(en)Monomeric eqFP611 variants exhibit red fluorescent properties and DNA encoding monomeric eqFP611 variants.

1.ApplicationNumber: US-200913131291-A
1.PublishNumber: US-8680238-B2
2.Date Publish: 20140325
3.Inventor: WIEDENMANN JOERG
KREDEL SIMONE
OSWALD FRANZ
NIENHAUS GERD ULRICH

4.Inventor Harmonized: WIEDENMANN JOERG(DE)
KREDEL SIMONE(DE)
OSWALD FRANZ(DE)
NIENHAUS GERD ULRICH(DE)

5.Country: US
6.Claims:
(en)Monomeric eqFP611 variants exhibit red fluorescent properties and DNA encoding monomeric eqFP611 variants.

7.Description:
(en)RELATED APPLICATIONS
This is a §371 of International Application No. PCT/EP2009/008413, with an international filing date of Nov. 26, 2009 (WO 2010/060618 A1, published Jun. 3, 2010), which is based on U.S. Patent Application No. 61/118,130, filed Nov. 26, 2008, the subject matter of which is incorporated by reference.
SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Jan. 5, 2012, is named RUF081US.txt and is 30,199 bytes in size.
TECHNICAL FIELD
This disclosure relates to monomeric variants of the red fluorescent protein eqFP611 (Genbank accession number AY130757) exhibiting a comparatively large Stokes shift in the orange red region of the spectrum between 557 and 630 nm, and their versatile fields of application in biology, in particular live-cell imaging.
BACKGROUND
Fluorescent proteins (FPs) are powerful, specific marker tools for cellular imaging, and their range of applications is continuously expanding (1). Red fluorescent proteins (RFPs) are of particular interest as they extend the color palette for multi-channel and FRET (fluorescence resonance energy transfer) imaging, and the reduced scattering of long-wavelength light makes them attractive as markers for deep-tissue imaging. A performance gap has been noticed for natural RFPs after isolation from marine invertebrates (2-4), in comparison to variants of the classical green fluorescent protein (GFP) (1). In particular, their tendency to form dimers or tetramers can be detrimental for fusion marker applications (4-6). Therefore, an entire “fruit basket” of monomeric FPs in many different hues was engineered from the tetrameric RFP DsRed (1, 7-8). Together with monomeric variants of GFP, eqFP578 and several reef coral proteins, the emission colors of these FPs cover a wide range from blue to red (1, 6, 9-10). Bright far-red fluorescent markers with emission maxima shifted up to 639 nm were developed on the basis of the Entacmaea quadricolor proteins eqFP578 (11).
Important FP applications are in biosensors that report on intracellular conditions via fluorescence resonance energy transfer (FRET) between two or more chromophors (1, 9-10). A large Stokes shift, i.e., a large wavelength separation between excitation and emission peaks assists in channel separation and facilitates the use of FPs in FRET-based applications, in multi-color imaging application and in whole-body and deep tissue imaging. Several red fluorescent proteins with Stokes shifts >47 are characterized by excitation/emission peaks beyond 582/629 nm. In contrast, there is no fluorescent protein known which exhibits a comparably large Stokes shift in the orange red region of the spectrum between 557 and 630 nm.
Accordingly, it could be helpful to provide novel monomeric fluorescent proteins having a comparably large Stokes shift in the orange red region of the spectrum between 557 and 630 nm, in particular to facilitate biological imaging or imaging applications.
SUMMARY
We provide a monomeric variant of red fluorescent protein eqFP611 including an altered amino sequence having at least one amino acid exchange selected from the group consisting of M12K, M15L, Y22H, D31E, V461, K67R, H72Y, T73P, F102I, K120Q, L147M, S158T, Q159H, N163K, Y169H, E185G, F187I, F192I, F194A, E175V, K207N, H214R, C222A, D223G, P225G, S226G and K227G.
We also provide a monomeric variant of red fluorescent protein eqFP611 including an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 3 and SEQ ID No. 5.
We further provide a fusion protein including a protein of interest fused to the monomeric variant of the red fluorescent protein eqFP611.
We still further provide a composition including the monomeric variant of the red fluorescent protein eqFP611 in a biologically compatible medium.
We further yet provide DNA encoding a monomeric variant of red fluorescent protein eqFP611 including an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 3 and SEQ ID No. 5.
We also further provide DNA including a nucleotide sequence selected from the group consisting of SEQ ID No. 2, SEQ ID No. 4 and SEQ ID No. 6.
We yet again provide an expression vector including expression control sequences operably linked to the DNA.
We further yet again provide a host cell including the DNA.
We also yet again provide a fluorescent reagent kit including at least one of a) DNA of SEQ ID No. 2, 4 or 6, b) an expression vector having DNA of SEQ ID No. 2, 4 or 6, and c) a host cell having DNA of SEQ ID No. 2, 4 or 6.
We still yet again provide a method for preparing a monomeric variant of red fluorescent protein eqFP611 including a) cultivating the host cell so that the host cell produces a monomeric variant of the red fluorescent protein eqFP611, and b) isolating and purifying the monomeric variant so produced by the host cell.
We also provide a method for selecting cells expressing a protein of interest including (a) introducing into cells DNA encoding a protein of interest and DNA encoding the monomeric variant of the red fluorescent protein eqFP611, (b) cultivating the cells from (a) under conditions permitting expression of the monomeric variant and the protein of interest, and (c) selecting cultivated cells from (b) which express the monomeric variant.
We also provide a method for measuring expression of a protein of interest in a cell including (a) introducing into a cell DNA encoding the monomeric variant of the red fluorescent protein eqFP611 fused to DNA encoding a protein of interest, the DNA being operably linked to and under control of an expression control sequence which moderates expression of the protein of interest, (b) cultivating the cell under conditions suitable for expression of the protein of interest, and (c) detecting fluorescence emission of the monomeric variant to measure expression of the protein of interest.
We also provide a method for determining localization of a protein of interest including (a) introducing into a cell DNA encoding the monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein of interest, the DNA being operably linked to and under control of a suitable expression control sequence, (b) cultivating the cell under conditions suitable for expression of the protein of interest; and (c) determining localization of the protein of interest by detecting fluorescence emission of the monomeric variant by optical means.
We also provide a method for localizing a subcellular structure in a cell including (a) introducing into a cell DNA encoding the monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein specific for a subcellular structure, the DNA being operably linked to and under control of an expression control sequence which moderates expression of the protein specific for a subcellular structure, (b) cultivating the cell under conditions suitable for expression of the protein specific for a subcellular structure; and (c) detecting fluorescence emission of the monomeric variant to localize the subcellular structure in the cell.
We also provide a method of comparing an effect of one or more test substance(s) on expression and/or localization of a protein of interest including (a) introducing, into a cell DNA encoding the monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein of interest, the DNA being operably linked to and under control of a suitable expression control sequence, (b) cultivating the cell under conditions suitable for expression of the protein of interest in the presence and absence of the test substance(s), (c) determining expression and/or localization of the protein of interest by detecting fluorescence emission of the monomeric variant by optical means, and (d) comparing the fluorescence emission obtained in the presence and absence of the test substance(s) to determine the effect of the test substance(s) on the expression and/or localization of the protein of interest.
We also provide a method for determining promoter activity in a cell including (a) introducing into a cell a vector that is constructed such that DNA encoding the monomeric variant of the red fluorescent protein eqFP611 is located downstream of a promoter to be tested, and (b) detecting fluorescence of the monomeric variant to determine activity of the promoter.



BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1A-F show the following: Subcellular localization of eqFP611 variants in HEK293 cells (A). The eqFP611 dimer 1 (RFP611, T122R) (13) is evenly distributed over the cell (B). The enhanced eqFP611 dimer 2 (T122G, F194A) shows a granular localization. (C-F) Cells co-expressing EGFP-SKL and an enhanced monomeric eqFP611 (T122R, F194A) variant show co-localization of green and red fluorescence in the peroxisomes. (C) Phase contrast image. (D) Green-channel image acquired with a standard FITC filter set. (E) Red-channel image product with a standard TRITC filter set. (F) Overlay image of the green and red channels. Bars: 2.5 μm.
FIGS. 2A-G show the following: Characterization of a monomeric eqFP611 variant (as set forth in SEQ ID No. 1, denoted as mRuby). (A) In vitro chromophore maturation at 37° C. as determined from the fluorescence emission at 605 nm (solid line: exponential fit). (B) Elution volume for concentrations of 4-30 mg/ml (0.16-1.2 mM) during gel-filtration analysis (standards for the oligomerization degree: GFP S65T, monomer; td-RFP611, dimer; eqFP611, tetramer). (C) Absorption, excitation and emission spectra (inset: fluorescence decay with exponential fit yielding a lifetime of 2.6±0.1 ns). (D) Absorption spectra at various pH values (inset: absorption at 558 nm versus pH; Henderson-Hasselbalch fit reveals a pKa of 4.4). (E) The increasing absorption at about 390 nm along with the decrease of the about 463 nm band of the protonated chromophore of the monomeric eqFP611 variant indicates the destruction of the acylimine bond of the chromophore over a period of 3.5 h time at pH 1.3. (F) Changes in the absorption spectrum of the monomeric eqFP611 variant during a 1-h time course of alkaline denaturation at pH 13. (G) Time-dependent fluorescence decay of the monomeric eqFP611 variant at pH 13 in comparison to other monomeric fluorescent proteins, measured, at their emission maxima.
FIGS. 3A-B show the following: Applications of a monomeric eqFP611 variant (as set forth in SEQ ID No. 1) as cellular marker proteins. (A) Epifluorescence image of NIH3T3 cells expressing the monomeric eqFP611 variant fused to human α-tubulin. Two cells from a single image were arranged in closer proximity. (B) Spinning-disk confocal image of the endoplasmic reticulum of a HeLa cell stained with ER-monomeric-eqFP611-variant-KDEL (“KDEL” disclosed as SEQ ID No. 7). False colors encode fluorescence intensity.
FIGS. 4A-C show the following: Peroxisome clusters in HEK293 cells. (A-C) Confocal images (Leica TCS 4Pi) of HEK293 cells co-expressing monomeric eqFP611 variant-PTS and H 2 B-EGFP during (A) interphase and (B) metaphase. The inset in (B) shows a magnification of a peroxisomal cluster. Tubulin fibers are labeled in green with Alexa Fluor®-488 via an anti-α-tubulin antibody (C) to reveal peroxisomal clustering at the spindle poles. Bars: 2 μm.
FIG. 5 shows the following: Inheritance of peroxisomes. Distribution of peroxisomes during different stages of mitosis in HeLa (upper row) and NIH3T3 cells (lower row). Peroxisomes are highlighted by monomeric eqFP611 variant-PTS. The spindle of the mitotic cells is stained with EGFP fused to a tubulin-binding protein [13]. Images were taken 24-48 h after transfection on an Olympus IX71 microscope equipped with standard FITC and TRITC filter sets. Bars: 5 μm.
FIGS. 6A-B show the following: Stability of a monomeric eqFP611 variant (as set forth in SEQ ID No. 1 denoted as mRuby) targeted to the endoplasmic reticulum (ER). (A) Comparison of ER-staining in HeLa cells expressing ER-EGFP-KDEL (“KDEL” disclosed as SEQ ID No. 7) (left column), ER-monomeric eqFP611 variant-KDEL (“KDEL” disclosed as SEQ ID No. 7) (right column) or both (middle column). Imaging of the EGFP fluorescence in the green channel (upper row) required exposure times of 4.0 s whereas fluorescence of the monomeric eqFP611 variant in the red channel could be already recorded with exposure times of 0.4 s using an Olympus IX71 microscope equipped with standard FITC (green channel) and TRITC (red channel) filter sets. (B) Magnified view of a HeLa cell expressing ER-monomeric eqFP611 variant-Kdel (“Kdel” disclosed as SEQ ID No. 7) photographed on the Olympus IX71 microscope with TRITC filter. Bars: 2 μm.
FIG. 7 displays a multiple sequence alignment of monomeric red fluorescent proteins and their tetrameric predecessors (SEQ ID Nos. 23, 1 and 24-29, respectively, in order of appearance). Modified amino acid residues are highlighted in different colors; cyan: residues involved in interface interactions; green: residues in the interior of the β-can; magneta: residues interacting with the chromophore; yellow: external residues; gray: GFP-termini of mCherry. The chromophore is underlined; β-strands are indicated by arrows.



DETAILED DESCRIPTION
We provide a monomeric variant of the red fluorescent protein eqFP611 having an altered amino sequence featuring at least one of the amino acid exchanges selected from the group consisting of M12K, M15L, Y22F1, D31E, V46I, K67R, H72Y, T73P, F102I, K120Q, L147M, S158T, Q159H, N163K, Y169H, E185G, F187I, F192I, F194A, E175V, K207N, H214R, C222A, D223G, P225G, S226G and K227G.
The numbering of the above listed amino acid exchanges are based on the amino acid sequence of eqFP611 deposited under genbank accession number AY130757. Further, amino acids are described using the single letter code. In this regard, for instance the term “M12K” means that the amino acid M (methionine) at position 12 from the eqFP611 has been exchanged by the amino acid K (lysine).
More specifically, we provide a monomeric variant of the red fluorescent protein eqFP611 having an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 3 and SEQ ID No. 5. In this regard, the monomeric rqFP611 variant as set forth in SEQ ID No. 3 is a codon optimized variant of the monomeric eqFP611 variant as set forth in SEQ ID No. 1. The monomeric eqFP611 variant as set forth in SEQ ID No. 5 carries the C-terminal tail of eqFP611 as a natural peroxisomal targeting signal.
The monomeric red fluorescent proteins are created from the tetrameric red fluorescent protein eqFP611 from the sea anemone Entacmaea quadricolor (Genbank accession number AY130757). The monomeric eqFP611 variants are in particular useful as labeling substances, preferably for live-cell imaging as well for imaging of fixed cells. The fluorescent proteins are characterized by advantageous properties such as red fluorescence with a large Stokes shift, monomeric nature, functional expression at 37° C., functional localization in the endoplasmic reticulum of mammalian cells, functional expression in fusion with tubulin in NIH3T3 cells, superior stability of fluorescence in cells fixed with paraformaldehyde and superior stability at extreme pH values. Moreover, a variant is presented that allows labeling of peroxisomes in eukaryotic cells.
The F102I variant of the tetrameric eqFP611 was chosen as the starting material for the development of a monomeric variant owing to its excellent expression at 37°. Introduction of amino acids 122 arginine and 194 alanine, which were known to disrupt the A/B and A/C subunit interactions in tetrameric DsRed and eqFP611 (7, 12), resulted in a nearly complete loss of fluorescence. In several rounds of random and multi-site-directed mutagenesis, the fluorescence was recovered by replacing amino acids that apparently impeded proper folding and maturation of the chromophor. In HEK293 cells transfected with these monomeric eqFP611, variants, the red fluorescence was not evenly distributed but rather appeared as dot-like structures in the cytoplasm. This localization resembled closely the aggregates reported for several non-soluble GFP-like proteins such as dsRed. In-depth analysis of the sequence and observation of the behavior of the “aggregates” during the cell cycle revealed that exposure of the A/C interface during monomerization exposed a subcellular targeting signal that directs the protein in cellular organelles, namely the amino acid sequence 229 GRL 231 at the C terminus of the monomeric eqFP611 variant as set forth in SEQ ID No. 5, and also the preceding triplet 226 SKL 228 serve as (type-1) peroxisomal targeting signal (PTS) (13). The presence of a functional PTS was verified by imaging HEK293 cells co-transfected with monomeric eqFP611 as set forth in SEQ ID No. 5 and EGFP-SKL, an established peroxisomal marker. Both green and red fluorescence showed perfect co-localization ( FIG. 1 ): We succeeded in removing peroxisomal targeting by replacing the C-terminal sequence 222 CDLPSKLGRL 231 (SEQ ID No. 8) of eqFP611 by 222 AGLGGG 227 (SEQ ID No. 9); amino acid modification and even truncation of the 229 GRL 231 tripeptide did not suffice (Supplemental Table 1). After completion of seven rounds of random mutagensis and four rounds of multi site-directed mutagenesis, a bright red-fluorescent monomer as set forth in SEQ ID No. 1 was finally obtained. Compared to wild-type eqFP611, it contains altogether 28 amino acid replacements and is shorter by four amino acids. Additional mutations may be introduced. For instance at least one amino acid exchange selected from the group Consisting of N2Y/K/D, S3P, L4M, K6Q/E, N8K, M11T, M12K/V/R/L, M15V/L, E16D, Y22H, T27I, E29K, D31E, N33 S/K, Y35F, M36L/V/K, K44N/R/Q, V46I/A, I57V, K67R, H72Y, T73S/P, I76V/F, S83T, D98E, F102I/L/V, V104A, M105I, E111V, D112G, C114S, Y117H, A119V, K120R/Q, T122R/A/G/M, S128A/P, N129H/D, Q134R, K136R, M146I, L147M, Y148C, D151N, Y157H/F, S158T, Q159H, A161V, N163K/R, D165E, Y169H, S171F/Y, S173F, E175V, T183S/A, V184D/I, E185G, N186Y, F187I/L, K188Q/E, G191D, F192I/Y, F194A/V/T, H197Y, E204D, S205R, D206G, K207D/N/Q/E, M209K/T, Q213L, H214R, H216R/Y, V218E, F221I/S/L/Y, C222W/Y/G/C, L224P, P225S and L231P may be introduced in a monomeric variant of the fluorescent protein eqFP611. These amino acid sequences may further improve folding of monomeric eqFP611 variants. To further improve the performance of the monomeric eqFP611 variant as set forth in SEQ ID No. 1 in live-cell imaging applications, the codon usage of the final variant was altered to facilitate expression. By this method, the fluorescence in mammalian cells could be increased by 5-8 fold. The codon optimized variant as set forth in SEQ ID No. 3 is particularly useful for labeling purposes in sensitive systems such as primary cell cultures or stem cells.
The following properties relate to the monomeric eqFP611 variant as set forth in SEQ ID No. 1 and 3. At 37° C., fluorescence spectrometry on dilute solutions of the purified protein yields a half-maturation time of 2.8 h, which makes the protein suitable for most cell biological imaging applications ( FIG. 2A ). A tendency to dimerize was absent in the entire range of physiologically relevant concentrations ( FIG. 2B ). With excitation and emission maxima at 558 nm and 605 nm, respectively, the eqFP611 variant combines a monomeric nature with a uniquely large Stokes shift in the orange-red emission region ( FIG. 2C , Supplementary Table 2). Its fluorescence lifetime of 2.6±0.1 ns is comparatively long for a monomeric red fluorescent protein (6), and together with its high quantum yield (0.35) and molar extinction coefficient of 112,000 M −1 cm −1 , the monomeric eqFP611 variant appears as superb marker in the red spectral range. It may be especially useful for FRET applications, where it bridges the gap between yellow-orange and far-red fluorescent proteins. The photobleaching probability of the monomeric eqFP611 variant (5.3×10 −6 ) is very similar to the one of its predecessor RFP611 (4.9×10 −6 ). The engineering process has significantly improved the stability of the monomeric eqFP611 variant at pH extremes as compared to tetrameric eqFP611. Below pH 5, the monomeric eqFP611 variant chromophore becomes protonated, as indicated by the increasing absorption band at 463 nm ( FIG. 2D ), but the protein remains stable even at pH 3. In contrast, the eqFP611 chromophore decomposes quickly at pH 3, as witnessed by the appearance of a 390-nm absorption band indicative of the neutral GFP (Green Fluorescent Protein) chromophore. At pH 13, the fluorescence of a variety of monomeric fluorescent proteins including EGFP (Enhanced Green Fluorescent Protein) disappears within seconds, whereas the fluorescence of the monomeric eqFP611 variant takes about an hour to vanish completely ( FIGS. 2E-G ). This stability at pH extremes makes the monomeric eqFP611 variant suitable for imaging of cellular organelles with pH values deviating from the standard physiological pH around pH 7. The stability of the monomeric eqFP611 variant is further beneficial for imaging of cells fixed with paraformaldehyde: The fluorescence of cells fixed in paraformaldehyde after expressing the state-of-the-art red fluorescent marker protein “mCherry” steadily faded in course of three weeks. In contrast, the fluorescence of cells expressing the monomeric eqFP611 variant slightly increased under the same experimental conditions. This property makes the monomeric eqFP611 variant an ideal marker for applications that rely on tracking of labeled cells or proteins in tissue fixed with paraformaldehyde.
To examine the performance of the monomeric eqFP611 variant (as set forth in SEQ ID No. 1 or 3) as a marker in live-cell imaging applications, it was fused to the N-terminus of α-tubulin because imaging of microtubules with such a fusion construct is known to be very sensitive to oligomerization, aggregation tendency and C-terminal amino acid linker properties of the marker protein (8). FIG. 3A exemplifies an excellent performance of the monomeric variant in highlighting tubulin fibers. Another challenging application, which requires a high stability of the marker protein, is its localization in the endoplasmic reticulum (ER). The construct ER-monomeric eqFP611 variant-KDEL (“KDEL” disclosed as SEQ ID No. 7) yielded excellent images of the ER with only 0.4 s light exposure in both epifluorescence and confocal microscopy modes ( FIG. 3B , FIGS. 6A-B ), whereas the popular marker protein EGFP targeted to the ER (ER-EGFP-KDEL (“KDEL” disclosed as SEQ ID No. 7)) required much longer exposure times under comparable conditions ( FIGS. 6A-B ).
Peroxisomes are the organelles that have been discovered last, and despite their essential functional roles in eukarytotic cells (13), many aspects of their biology are still not well understood (13). The present observation with the early monomeric eqFP611 variant as set forth in SEQ ID No. 5 that highlighted two peroxisome clusters during mitosis of HEK293 cells suggests an ordered partitioning of this organell to daughter cells. This finding contrasts the commonly held view that peroxisomes are distributed stochastically between dividing mammalian cells (14). Hence, it was further explored the issue of peroxisorrie inheritance in mammalian cells. To this end, the original C-terminal sequence of eqFP611 in the monomeric eqFP611 variant as set forth in SEQ ID No. 5 was restored to attain an efficient peroxisomal marker (monomeric eqFP611-PTS). HEK293 cells were co-transfected with monomeric eqFP611-PTS and the chromatin-binding histone 2B protein (H 2 B) fused to EGFP (1) so as to simultaneously image peroxisomes (in red) and chromatin (in green). During interphase, peroxisomes were seen to be evenly distributed over the cytoplasm ( FIG. 2C ). However, at the beginning of metaphase, peroxisomes began to congregate in two clusters on the bottom and top of the emerging metaphase plate ( FIG. 2D ). Additional immunochemical staining of the mitotic spindle revealed that the peroxisomes clustered around the spindle poles ( FIG. 2E ). By this ordered partitioning strategy, the cells can ensure that equal numbers of peroxisomes are inherited by the daughter cells. It was further examined this mechanism with two other mammalian cell lines, HeLa and NIH3T3. In HeLa cells, peroxisomes were also closely associated with the spindle pole during all stages of cell division ( FIG. 5 ). By contrast, NIH3T3 cells showed these peroxisomal associations to the centrosomes only during two stages of cell division, anaphase and telophase.
We also provided a monomeric variant of the red fluorescent protein having an amino acid sequence comprising a deletion, substitution and/or addition of one or several amino acids with respect to the amino acid sequence selected from the group consisting of SEQ ID No. 1, 3 and 5 and having red fluorescent properties.
The range of “1 to several” in “an amino acid sequence comprising a deletion, substitution, and/or addition of one or several amino acids” is not particularly limited but means, for example, about 1 to 20, preferably 1 to 10, more preferably 1 to 7, furthermore preferably 1 to 5, and particularly preferably 1 to 3.
We also provide a fusion compound, preferably a fusion protein, comprising a protein of interest fused to a monomeric variant of the red fluorescent protein eqFP611. The type of protein of interest with which the monomeric eqFP611 variant is fused is not particularly limited. Preferred examples may include proteins localizing in cells, proteins specific for intracellular structures, in particular intracellular organelles and targeting signals (e.g., a nuclear transport signal, a mitochondrial presequence and the like). The obtained fusion protein wherein the monomeric eqFP611 variant is fused with a protein of interest is allowed to be expressed in cells. By monitoring a fluorescence emitted it becomes possible to analyze the activity, localization, processing, or dynamics of the protein of interest in cells. That is, cells transformed or transfected with DNA encoding the monomeric eqFP611 variant are observed with the fluorescence microscope, so that the activity, localization, processing and dynamics of the protein of interest in the cells can visualized and thus analyzed.
The term “protein of interest” is intended also to encompass polypeptides and peptide fragments. Examples of such proteins of interest include: NFκB and subunits thereof, RAC1, PLC domains, MAPKAP2, PKC, Cytochrome C, RHO, β-actin, α-tubulin, STAT6 and protein kinase C isotypes.
We further provide a composition comprising a monomeric eqFP611 variant and a suitable biologically compatible medium. Examples of suitable biologically compatible media include: Nutritive media, buffer solutions, pharmaceutically acceptable carriers.
We still further provide DNA encoding a monomeric variant of the red fluorescent protein eqFP611 having an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 3 and SEQ ID No. 5.
The DNA may have a nucleotide sequence selected from the group consisting of SEQ ID No. 2, SEQ ID No. 4 and SEQ ID No. 6.
Furthermore, we address a nucleotide sequence comprising a deletion, substitution and/or addition of one or several nucleotides with respect to the nucleotide sequence as set forth in SEQ ID No. 2, 4 or 6. The range of “1 to several” in “a nucleotide sequence comprising a deletion, substitution and/or addition of one or several nucleotides” is not particularly limited but means, for example, about 1 to 50, preferably 1 to 30, more preferably 1 to 20, furthermore preferably 1 to 10, and particularly preferably 1 to 5.
The DNA may be prepared synthetically by establishes methods, e.g., the phosphoramidite method (15, 16). According to the phosphoramidite method, oligonucleotides are synthesized, e.g., in an automatic DNA synthesizer, purified, annealed, ligated and cloned into suitable vectors. The DNA may also be prepared by recombinant DNA methodology (17). The DNA may also be prepared by polymerase chain reaction (PCR) (18).
The method of introducing a desired mutation into a predetermined nucleotide sequence is known. For example, DNA having the mutation can be constructed by appropriately using known techniques such as site specific mutagenesis method, PCR using degenerate oligonucleotides, and exposure of cells containing the nucleic acid to a mutagen or radiation (19, 20).
The DNA sequence encoding a monomeric eqFP611 variant may be joined in-frame with a gene encoding a protein of interest and the desired fusion protein produced when inserted into an appropriate expression vector. For example, polymerase chain reaction or complementary oligonucleotides may be employed to engineer a polynucleotide sequence corresponding to a monomeric eqFP611 variant, 5′ or 3′ to the gene sequence corresponding to the protein of interest. Alternatively, the same techniques may be used to engineer a polynucleotide sequence corresponding to the sequence of a monomeric eqFP611 variant 5′ or 3′ to the multiple cloning site of an expression vector prior to insertion of a gene sequence encoding the protein of interest. The polynucleotide sequence corresponding to the sequence of a monomeric eqFP611 may comprise additional nucleotide sequences to include cloning sites, linkers, transcription and translation initiation and/or termination signals, labeling and purification tags.
In a further aspect, there is provided an expression vector comprising suitable expression control sequences operably linked to a DNA molecule. The DNA may be inserted into a recombinant vector, which may be any vector that may be conveniently be subjected to recombinant DNA procedures. The choice of vector will often depend on the host cell into which it is to be introduced. Thus, the vector may be an autonomously replicating vector, e.g., a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid. Alternatively, the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated.
The vector is preferably an expression vector in which the DNA sequence encoding a monomeric eqFP611 variant is operably linked to additional segments required for transcription of the DNA. In general, the expression vector is derived from plasmid or viral DNA, or may contain elements of both. The term, “operably linked” indicates that the segments are arranged so that they function in concert for their intended purposes, e.g., transcription initiates in a promoter and proceeds through the DNA sequence coding for a monomeric eqFP611 variant. The promoter may be any DNA sequence which shows transcriptional activity in a suitable host cell of choice, (e.g., a bacterial cell, a mammalian cell, a yeast cell, or an insect cell) for expressing a monomeric eqFP611 variant of the invention. The promoter may be derived from genes encoding proteins either homologous or heterologous to the host cell.
Examples of suitable promoters for directing the transcription of the DNA sequence encoding the monomeric eqFP611 variant are the CMV promoter, Ubiquitin C promoter, SV40 promoter and MT-1 (metallothionein gene) promoter. An example of a suitable promoter for use in insect cells is the polyhedron promoter. Examples of suitable promoters for use in yeast host cells include promoters from yeast glycolytic genes or alcohol dehydrogenase genes or ADH2-4-c promoters. Examples of suitable promoters for use in bacterial host cells include the promoter of the Bacillus stearothermophilus maltogenic amylase gene, the Bacillus licheniformis alpha-amylase gene, the Bacillus amyloliquefaciens BAN amylase gene, the Bacillus subtilis alkaline protease gene, or the Bacillus pumilus xylosidase gene, or the phage Lambda PR or PL promoters or the Escherichia coli lac, trp or tac promoters.
The DNA sequence encoding a monomeric eqFP611 variant may also, if necessary, be operably connected to a suitable terminator, such as the human growth hormone terminator or the TPI1 or ADH3 terminators. The vector may further comprise elements such as polyadenylation signals (e.g., from SV40 or the adenovirus 5 E1b region), transcriptional enhancer sequences (e.g., the SV40 enhancer) and translational enhancer sequences (e.g., the ones encoding adenovirus VA RNAs).
The recombinant vector may further comprise a DNA sequence enabling the vector to replicate in the host cell in question. An example of such a sequence (when the host cell is a mammalian cell) is the SV40 origin of replication. When the host cell is a yeast cell, examples of suitable sequences enabling the vector to replicate are the yeast plasmid 2μ replication genes REP 1-3 and origin of replication. The vector may also comprise selectable markers, such as a gene that confers resistance to a drug, e.g., ampicillin, kanamycin, tetracyclin, chloramphenicol, puromycin, neomycin or hygromycin.
A further aspect relates a host cell having the DNA. Preferably, the host cell is transformed or transfected with a DNA construct comprising an expression vector. The DNA construct or the recombinant vector is suitably introduced into a host cell which may be any cell which is capable of expressing the present DNA construct and includes bacteria, yeast and higher eukaryotic, in particular mammalian, cells.
Examples of bacterial host cells which, on cultivation, are capable of expressing the DNA construct are Gram-positive bacteria, e.g., species of Bacillus or Gram-negative bacteria such as E. coli . The transformation of the bacteria may be effected by using competent cells in a known manner.
Examples of suitable mammalian cell lines are the HEK293 and the HeLa cell lines, primary cells, and the COS (e.g., ATCC CRL 1650), BILK (e.g., ATCC CRL 1632, ATCC CCL 10), CHL (e.g., ATCC CCL 39) or CHO (e.g., ATCC CCL 61) cell lines. Methods of transforming or transfecting mammalian cells and expressing DNA sequences introduced in the cells are known (21-23).
Examples of suitable yeast cells include cells of Saccharomyces spp. or Schizosaccharomyces spp., in particular strains of Saccharomyces cerevisiae or Saccharomyces kluyveri . Transformed cells may be selected by a phenotype determined by a selectable marker, commonly drug resistance or the ability to grow in the absence of a particular nutrient, e.g., leucine. A preferred vector for use in yeast is the POT1 vector. The DNA sequence encoding a monomeric eqFP611 variant may be preceded by a signal sequence and optionally a leader sequence, e.g., as described above. Further examples of suitable yeast cells are strains of Kluyveromyces , such as K. lactis, Hansenula , e.g., H. polymorpha , or Pichia , e.g., P. pastoris (24).
There is further provided a fluorescent reagent kit comprising at least one of: a) the DNA of SEQ ID No. 2, 4 or 6 b) an expression vector having the DNA of SEQ ID No. 2, 4 or 6 and c) a host cell having the DNA of SEQ ID No. 2, 4 or 6.
Further, there is provided a method for preparing a monomeric variant of the red fluorescent protein eqFP611, the method comprising:
(a) cultivating a host cell so that the host cell produces a monomeric variant of the red fluorescent protein eqFP611; and (b) isolating and purifying said monomeric variant so produced by the host cell.

Suitably, the host cells, generally transformed or transfected as described above, are cultured in a suitable nutrient medium under conditions permitting the expression of a DNA encoding a monomeric eqFP611 variant. After completion of the culture, the cells may be recovered by centrifugal separation, and the recovered cells may be suspended in a water type buffer. Thereafter, the cells are typically disintegrated using an ultrasonic disintegrator or the like, so as to obtain a cell-free extract. A supernatant is obtained by centrifuging the cell-free extract, and then, a purified sample can be obtained from the supernatant by applying, singly or in combination. For instance, the following ordinary protein isolation and purification methods may be applied: the solvent extraction, the salting-out method using ammonium sulfate or the like, the desalting method, the precipitation method using an organic solvent, the anion exchange chromatography using resins such as diethylaminoethyl (DEAE) sepharose, the cation exchange chromatography using resins such as S-Sepharose FF (manufactured by Pharmacia), the hydrophobic chromatography using resins such as butyl sepharose or phenyl sepharose, the gel filtration method using a molecular sieve, the affinity chromatography, the chromatofocusing method and electrophoresis such as isoelectric focusing.
The medium used to culture the cells may be any conventional mediums suitable for growing the host cells, such as minimal or complex media containing appropriate supplements. Suitable media are available from commercial suppliers or may be prepared according to published protocols which are known.
We also provide a method for selecting cells expressing a protein of interest comprising:
(a) introducing into cells a DNA encoding a protein of interest and a DNA encoding a monomeric variant of the red fluorescent protein eqFP611; (b) cultivating the cells from (a) under conditions permitting expression of the monomeric variant and the protein of interest; and (c) selecting cultivated cells from (b) which express the monomeric variant.

We also encompass a method for measuring, in particular determining and/or monitoring, expression of a protein of interest in a cell comprising:
(a) introducing into a cell a DNA encoding a monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein of interest the DNA being operably linked to and under the control of an expression control sequence which moderates expression of the protein of interest; (b) cultivating the cell under conditions suitable for the expression of the protein of interest; and (c) detecting the fluorescence emission of the monomeric variant as a means for measuring, in particular determining and/or monitoring, the expression of the protein of interest.

The term “operably linked” means that the regulatory sequences necessary for expression of the coding sequence are placed in the DNA molecule in the appropriate positions relative to the coding sequence so as to effect expression of the coding sequence. The same definition is sometimes applied to the arrangement of coding sequences and transcription control elements (EG promoters, enhances, and termination elements) in an expression vector. This definition is also sometimes applied to the arrangement of nucleic acid sequences of a first and a second nucleic acid molecule wherein a highbred nucleic acid molecule is generated.
With respect to the above-mentioned method, the monomeric eqFP611 variants act as a fluorescent labeling substances. This is to say, the monomeric eqFP611 variant is preferably purified as a fusion protein with a protein of interest, and the fusion protein is introduced into cells by methods such as the microinjection. By observing the distribution of the fusion protein over time, targeting activity of the protein of interest can be detected in the cells.
As already mentioned, the type of the protein of interest with which the monomeric eqFP611 variant is fused is not particularly limited. Preferred examples may include proteins localizing in cells, proteins specific for intracellular structures, in particular organelles, and targeting signals (e.g., a nuclear transport signal a mitochondrial presequence and the like). For example, by using a protein specific for an intracellular structure in particular intracellular organella, as a protein of interest, the distribution and movement of nucleus, mitochondria, an endoplasmic reticulum, a Golgi body, a secretory vesicle, a peroxisome or the like can be observed.
Accordingly, we provide a method for determining the localization, in particular intra- and/or extracellular localization, of a protein of interest comprising:
(a) introducing into a cell a DNA encoding a monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein of interest the DNA being operably linked to and under the control of a suitable expression control sequence; (b) cultivating the cell under conditions suitable for the expression of the protein of interest; and (c) determining the localization of the protein of interest by detecting the fluorescence emission of the monomeric variant by optical means.

We further provide a method for localizing a subcellular structure in a cell comprising:
(a) introducing into a cell a DNA encoding a monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein or peptide specific for a subcellular structure the DNA preferably being operably linked to and under the control of an expression control sequence which moderates expression of the protein or the peptide specific for a subcellular structure; (b) cultivating the cell under conditions suitable for the expression of the protein or the peptide specific for a subcellular structure; and (c) detecting the fluorescence emission of the monomeric variant as a means for localizing the subcellular structure in the cell.

Suitable proteins ° being specific for cellular substructures, in particular organelles are proteins being specific for endoplasmic recticulum, peroxisomes, nucleus, in particular organelles with pH values deviating from 7. Alternatively, the peptide specific for a subcellular structure may be a targeting signal, in particular cellulare substructures, for instance peroxisomes, endoplasmic reticulum, nucleus, mitochondria and the like. To this means, a monomeric eqFP611 variant may be fused to the targeting signal for labeling of cellular substructures, in particular for labeling the aforementioned organelles.
Further, we provide a method of comparing the effect of one or more test substance(s) on the expression and/or localization of a protein of interest comprising:
(a) introducing into a cell a DNA encoding a monomeric variant of the red fluorescent protein eqFP611 fused to a DNA encoding a protein of interest the DNA being operably linked to and under the control of a suitable expression control sequence; (b) cultivating the cell under conditions suitable for the expression of the protein of interest in the presence and absence of the test substance(s); (c) determining the expression and/or localization of the protein of interest by detecting the fluorescence emission of the monomeric variant by optical means; and (d) comparing the fluorescence emission obtained in the presence and absence of the test substance(s) to determine the effect of the test substance(s) on the expression and/or localization of the protein of interest.

Finally, a method determines promoter activity in a cell comprising:
(a) introducing into a cell a vector that is constructed such that DNA encoding a monomeric variant of the red fluorescent protein eqFP611 is located downstream of a promoter to be tested; and (b) detecting the fluorescence of the monomeric variant as a means for determining the activity of the promoter.

The fluorescence of the monomeric eqFP611 variant can be detected with a viable cell or with fixed cells. Such detection can be carried out using, for example, a fluorescence microscope (Axiophoto Filter Set 09 manufactured by Carl Zeiss) or an image analyzer (Digital Image Analyzer manufactured by ATTO). The type of a microscope can be appropriately selected depending on purposes. Where frequent observation such as pursuit of a change over time is carried out, an ordinary incident-light fluorescence microscope is preferable. Where observation is carried out while resolution is emphasized, for example, in the case of searching localization in cells specifically, a confocal laser scanning microscope is preferable. In terms of maintenance of the physiological state of cells and prevention from contamination, an inverted microscope is preferable as microscope system. When an erecting microscope with a high-powered lens is used, a water immersion lens can be used. An appropriate filter set can be selected depending on the fluorescence wavelength of the monomeric eqFP611 variant. For example, since the wavelength of maximum absorption of the monomeric eqFP611 variant having the amino acid sequence as set forth in SEQ ID No. 1 is 558 nm, and the wavelength of maximum fluorescence thereof is 605 nm, circa 550 to 610 nm filter for fluorescence light can be used. Due to the large Stokes shift of the inventive monomeric eqFP611 variants, there is no cross-talk between the filters of a filter set when detecting the fluorescence of the monomeric eqFP611 variants.
Further, when viable cells are observed with time using a fluorescence microscope, photographing should be performed in a short time, and therefore a high sensitivity cooled CCD camera is used. In the cooled CCD camera, thermal noise is reduced by cooling CCD, and very weak fluorescent images can be clearly photographed with short-time exposure.
Alternatively or in combination to the above described fluorescence microscopy, the fluorescence may be detected by tracking, quantifying, and sorting of cells labeled with a monomeric eqFP611 variant using flow cytometry or fluorescence activated cell sorting (FACS).
To sum up, we provide novel monomeric variants of the red fluorescent protein eqFP611 exhibiting a large Stokes shift. This makes the monomeric variants in particular useful as labeling substances or markers (labels), preferably in biological and/or medicinal imaging. Preferably, the monomeric eqFP611 variants may be used as labeling substances for tracking cells, for instance in biological tissues or in cell cultures. The cells themselves may be living cells. Suitable cells may include differentiated cells and stem cells, particularly embryonic stem cells. Due to the superior stability of the monomeric eqFP611 variants upon fixation compounds, in particular paraformaldehyde, the monomeric variants of the tetrameric eqFP611 may also be used for labeling fixed cells. As already mentioned, the monomeric eqFP611 variants may further be used as labeling substances for selecting cells expressing a protein of interest. Furthermore, the monomeric eqFP611 variants may be used as labeling substances for measuring, in particular determining and/or monitoring, the expression, preferably the tissue specific expression, of a protein of interest. A further field of application of the monomeric eqFP611 variants relates to their use as labeling substances for determining and/or monitoring of cell differentiation, in particular stem cell differentiation, preferably embryonic stem cell differentiation. As already mentioned before, the monomeric eqFP611 variants may further be used as labeling substances for localization, in particular intra- and/or extracellular localization, of a protein of interest or for localization of a subcellular structure in a cell. Besides, the monomeric variants of eqFP611 may be used as markers for determining the promoter activity in a cell. A further area of application covers the use the inventive monomeric eqFP611 variants as labeling substances for measuring, in particular determining and/or monitoring, the gene expressions in cellular assays for screening of chemical compounds.
A preferred area of application relates to the use of the monomeric eqFP611 variants for diagnosing and/or monitoring of diseases. Preferably, the monomeric eqFP611 variants may be used in whole body imaging. For instance, the monomeric variants are used for monitoring of tumor development and/or for tracking of metastases. Furthermore, the monomeric eqFP611 variants may be used for determining and/or monitoring of peroxisomal biogenesis disorders.
The aforementioned fields of application impressively corroborate the versatility of the monomeric eqFP611 variants in the field of biology and medicine.
EXAMPLES
Example 1
Mutagenesis and Screening
The coding cDNA of tetrameric eqFP611 and its monomeric variants were ligated in the pQE-32 (Qiagen, Hilden, Germany). Monomerizing interface mutations were introduced by site-directed mutagenesis via overlap extension PCR (25). Random mutagenesis was performed according to the manufacturer's protocol using the Diversify PCR Random Mutagenesis Kit (Clontech Laboratories, Inc., Mountain View, Calif., USA), in conditions optimal for four to five mutations per 1000 bp. QuikChange Multi Site-Directed Mutagenesis Kit (Stratagene, La Jolla, Calif., USA) was used subsequently to spot mutations that act synergistically to promote folding. For this purpose, up to six oligonucleotide primers were applied in the mutagenesis reaction to a mixture of up to four different mutant templates. E. coli XL1-Blue or XL10-Gold® ultracompetent cells (Stratagene, La Jolla, Calif., USA) were transformed with the mutant plasmid libraries and bacterial colonies on agar plates were screened for fluorescence after overnight incubation at 37° C. using a UVA (365 nm) transilluminator (Benda, Wiesloch, Germany) and a fluorescence microscope (Axioplan I, Carl Zeiss Jena GmbH, Jena, Germany).
Example 2
Protein Expression, Purification and Gel Filtration Experiments
The eqFP611-variants carrying an N-terminal poly-His tag were expressed in E. coli M15 [pREP4] (Qiagen, Hilden, Germany). The proteins were purified using Talon™ metal affinity resin (Clontech Laboratories, Inc., Mountain View, Calif., USA) and gel filtration (Superdex 200, Äkta System, GE Healthcare Biosciences, Little Chalfont, UK) as described (4, 26).
Example 3
Determination of Maturation Times
Maturation times at 37° C. were determined as described (4). The protein solutions were diluted to ensure an OD ˜560 ˜0.1 after maturation to avoid artificially shortened maturation times due to inner filter effects. Maturation time courses at 37° C. were recorded with a Cary Eclipse Spectrofluorometer (Varian Inc., Palo Alto, Calif., USA).
Example 4
Spectroscopic Characterization
Absorption spectra were recorded on a Cary 50 Spectrophotometer (Varian Inc., Palo Alto, Calif., USA). Fluorescence emission and excitation spectra were measures with a Cary Eclipse Spectrofluorometer (Varian Inc., Palo Alto, Calif., USA). The spectral characterization of the monomeric eqFP611 variants at pH extremes and photobleaching experiments were conducted as described in literature (12). Fluorescence lifetime measurements on the monomeric eqFP611 variants were performed with a Zeiss Axiovert 135 inverted microscope (Carl Zeiss Jena GmbH, Jena, Germany) by using a computer card for time-correlated single-photon counting (TIMEHARP 200, Pico-Quant, Berlin, Germany) similar to previous reports (4). The excitation light pulses (532 nm) were generated by mode-locked, frequency-doubled solid-state laser (GE-100, Time Bandwidth Products, Zurich, Switzerland). The fluorescence quantum yield in 1×PBS, pH 7.0, was determined using eqFP611 (quantum yield of 0.45) as a reference (4). Measurements of the molar extinction coefficient using the alkaline denaturation method (Ward, 2005) failed because of the extraordinary stability of the monomeric eqFP611 variants. High concentrations of 0.3-1.0 N NaOH had been applied to denature the monomeric eqFP611 variants and to calculate the chromophore concentration by using the extinction coefficient of denatured GFP (Green Fluorescent Protein) at pH 13 (27). After complete denaturation, not only was the acylimine bond of the red chromophore reduced, but a significant fraction of the resulting GFP-chromophore was also destroyed, resulting in artificially high molar extinction coefficients of up to 250,000 M −1 cm −1 . Accordingly, the extinction coefficient of the monomeric eqFP611 variants were measured with the dynamic difference method.
Example 5
Vector Construction
For expression in mammalian cells, various monomeric eqFP611 variants were cloned into the pcDNA3 vector (Invitrogen, Carlsbad, Calif., USA). Human α-tubulin from the pEGFP-Tub vector (Clontech Laboratories, Inc., Mountain View, Calif., USA) was inserted into pcDNA3.1 (−) downstream of the coding sequence of monomeric eqFP611 variants (Invitrogen, Carlsbad, Calif., USA). An endoplasmic reticulum retention signal (KDEL (SEQ ID No. 7)) (28) was introduced to the C-terminus of the monomeric eqFP611 variant and EGFP by PCR. The PCR products were inserted into the expression vector pCI-leader, encoding the signal peptide (METDT-LLLW-VLLL-WVP-GSTGD (SEQ ID No. 10)) from the murine Igκ chain.
Example 6
Eukaryotic Expression and Imaging
HeLa and HEK293 cells were grown on chambered cover glasses (Nalge Nunc International Corp., Rochester, N.Y., USA). Images were taken 24-48 h post-transfection using fluorescene microscopes (DM IRB, Leica Microsystems, Wetzlar, Germany, IX71, Olympus, Hamburg, Germany) equipped with a digital camera (C4742, Hamamatsu, Japan), a 100-W mercury lamp and standard FITC and TRITC filter sets. Subcellular localization of monomeric eqFP611 variants with peroxisomal targeting signals (PTS) were assayed by confocal microscopy. HEK293 cells were transfected with a pcDNA3 vector encoding monomeric eqFP611 variant with a peroxisomal targeting signal alone or in combination with a pcDNA3 vector encoding EGFP-H2B. Cells were fixed, permeabilized, and used directly for microscopic analysis or after immunostaining with an antiserum directed against human α-tubulin and an Alexa Fluor® 488-coupled secondary antibody. Cells were plated on circular quartz coverslips (Leica Microsystems, Wetzlar, Germany). Sandwiches of two coverslips were assembled with PBS/glycerol (13%/87% by volume) as a mounting medium. Images were collected on a Leica TCS 4Pi scanning confocal laser microscope (Leica Microsystems, Wetzlar, Germany) using a 100×, NA 1.35, glycerol immersion objective and 488-nm excitation for EGFP and Alexa Fluor® 488, whereas monomeric eqFP611 variant was excited at 561 nm. The emitted photos were registered by using two avalanche photodiodes (APDs; SPCM-AQR-14, Perkin-Elmer, Canada). A maximum-intensity projection of a 3D stack was prepared for presentation.







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SUPPLEMENTAL TABLE 1



Peroxisomal localization of monomeric eqFP611

variants with different C-terminal sequences

in HEK293 cells.







Peroxisomal


SEQ
localization a







ID
24 h post-
48 h post-



trans-
trans-

C-terminal sequence
No.
fection
fection



_ 216 HAVAKFCDLPSKLGRL 231 b
11
++++++
++++++

_ 216 HAVAK HSGLL 225
12
+++++−
+++++−

_ 216 HAVAK HSGL 224
13
+++−−−
+++−−−

_ 216 HAVAKF AGL 224
14
−−−−−−
++−−−−

_ 216 HA E A Q F SGLL 225
15
−−−−−−
+−−−−−

_ 216 HAVAK HSG 223
16
−−−−−−
−−−−−−

_ 216 HAVAK HSGGG 225
17
−−−−−−
−−−−−−

_ 216 HA E A Q F SG 223
18
−−−−−−
−−−−−−

_ 216 HAVAKF CDL 224
19
−−−−−−
−−−−−−

_ 216 HAVAKF AGGG 225
20
−−−−−−
−−−−−−

_ 216 HAVAKF AGLGGG 227 c
21
−−−−−−
−−−−−−



a Rating based on the co-localization with EGFP-SKL from complete (++++++) to absent (−−−−−−)

b C-terminal sequence of wildtype eqFP611

c C-terminal sequence of monomeric eqFP variants as set forth in SEQ ID No. 1









































SUPPLEMENTAL TABLE 2 Fluorescence properties of monomeric eqFP variants as set forth in SEQ ID No. 1, its predecessors and other monomeric fluorescent proteins emitting in the orange to far-red spectral region. Excitation Emission Maximum Maximum Stokes E mol Relative FP Variant [nm] [nm] shift QY [M −1 cm −1 ] Brightness d mKO (Karasawa et al., 2004) 548 559 11 0.6 51,600 c 1.0 c mOrange (Shaner et al., 2004) 548 562 14 0.69 71,000 a 1.5 a tagRFP (Merzlyak et al., 2007) 555 584 29 0.48 100,000 a 1.5 a mRuby 558 605 47 0.35 not applicable a 1.2 b 112,000 b eqFP611 (Wiedenmann et al., 2002) 559 611 52 0.45 116,000 a 1.6 a 146,000 b 2.1 b RFP611 559 611 52 0.48 120,000 a 1.8 a 151,000 b 2.3 b mCherry (Shaner et al., 2004) 587 615 28 0.22 72,000 a 0.5 a mRaspberry (Wang et al., 2004) 598 625 27 0.15 86,000 a 0.4 a mKate (Shcherbo et al., 2007) 588 635 47 0.33 45,000 a 0.5 a mPlum (Wang et al., 2004) 590 649 59 0.1 41,000 a 0.1 a 143,400 b, c 0.4 b a Concentration of the red chromophore determined by the alkaline denaturation method (Gross et al., 2000). b Concentration of the red chromophore determined by the dynamic difference method. c Concentration of the red chromophore deduced from the protein concentration as determined by the Bradford test. d Product of QY and E mol compared to the brightness of EGFP (53,000M −1 cm −1 × 0.6) (Patterson et al., 1997).
Sequences (in Accordance with the Annexed Sequence Protocol)






SEQ ID No. 1 (denoted as mRuby):

MNSLIKENMRMKVVLEGSVNGHQFKCTGEGEGNPYMGTQTMRIKVIEGG



PLPFAFDILATSFMYGSRTFIKYPKGIPDFFKQSFPEGFTWERVTRYED



GGVITVMQDTSLEDGCLVYHAQVRGVNFPSNGAVMQKKTKGWEPNTEMM



YPADGGLRGYTHMALKVDGGGHLSCSFVTTYRSKKTVGNIKMPGIHAVD



HRLERLEESDNEMFVVQREHAVAKFAGLGGG.



SEQ ID No. 2 (denoted as mRuby):

ATGAATTCACTGATCAAGGAAAATATGCGTATGAAGGTGGTCCTGGAAG



GTTCGGTCAACGGCCACCAATTCAAATGCACAGGTGAAGGAGAAGGCAA



TCCGTACATGGGAACTCAAACCATGAGGATCAAAGTCATCGAGGGAGGA



CCCCTGCCATTTGCCTTTGACATTCTTGCCACGAGCTTCATGTATGGCA



GCCGTACTTTTATCAAGTACCCGAAAGGCATTCCTGATTTCTTTAAACA



GTCCTTTCCTGAGGGTTTTACTTGGGAAAGAGTTACAAGATACGAAGAT



GGTGGAGTCATTACCGTTATGCAGGACACCAGCCTTGAGGATGGCTGTC



TCGTTTACCACGCCCAAGTCAGGGGGGTAAACTTTCCCTCCAATGGTGC



CGTGATGCAGAAGAAGACCAAGGGTTGGGAGCCTAATACAGAGATGATG



TATCCAGCAGATGGTGGTCTGAGGGGATACACTCATATGGCACTGAAAG



TTGATGGTGGTGGCCATCTGTCTTGCTCTTTCGTAACAACTTACAGGTC



AAAAAAGACCGTCGGGAACATCAAGATGCCCGGTATCCATGCCGTTGAT



CACCGCCTGGAAAGGTTAGAGGAAAGTGACAATGAAATGTTCGTAGTAC



AACGCGAACACGCAGTTGCCAAGTTCGCCGGGCTTGGTGGTGGTTAA



SEQ ID No. 3 (denoted as mRuby, codon

optimized variant):

MNSLIKENMRMKVVLEGSVNGHQFKCTGEGEGNPYMGTQTMRIKVIEGG



PLPFAFDILATSFMYGSRTFIKYPKGIPDFFKQSFPEGFTWERVTRYED



GGVITVMQDTSLEDGCLVYHAQVRGVNFPSNGAVMQKKTKGWEPNTEMM



YPADGGLRGYTHMALKVDGGGHLSCSFVTTYRSKKTVGNIKMPGIHAVD



HRLERLEESDNEMFVVQREHAVAKFAGLGGG*



SEQ ID No. 4 (denoted as mRuby, codon

optimized variant):

ATGAACAGCCTGATCAAAGAAAACATGCGGATGAAGGTGGTGCTGGAAG



GCAGCGTGAACGGCCACCAGTTCAAGTGCACCGGCGAGGGCGAGGGCAA



CCCCTACATGGGCACCCAGACCATGCGGATCAAAGTGATCGAGGGCGGA



CCTCTGCCCTTCGCCTTCGACATCCTGGCCACATCCTTCATGTACGGCA



GCCGGACCTTCATCAAGTACCCCAAGGGCATCCCCGATTTCTTCAAGCA



GAGCTTCCCCGAGGGCTTCACCTGGGAGAGAGTGACCAGATACGAGGAC



GGCGGCGTGATCACCGTGATGCAGGACACCAGCCTGGAAGATGGCTGCC



TGGTGTACCATGCCCAGGTCAGGGGCGTGAATTTTCCCAGCAACGGCGC



CGTGATGCAGAAGAAAACCAAGGGCTGGGAGCCCAACACCGAGATGATG



TACCCCGCTGACGGCGGACTGAGAGGCTACACCCACATGGCCCTGAAGG



TGGACGGCGGAGGGCACCTGAGCTGCAGCTTCGTGACCACCTACCGGTC



CAAGAAAACCGTGGGCAACATCAAGATGCCCGGCATCCACGCCGTGGAC



CACCGGCTGGAAAGGCTGGAAGAGTCCGACAACGAGATGTTCGTGGTGC



AGCGGGAGCACGCCGTGGCCAAGTTCGCCGGCCTGGGCGGAGGGTGA



SEQ ID No. 5 (denoted as mRuby, with peroxisomal

targeting signal):

MNSLIKENMRMKVVLEGSVNGHQFKCTGEGEGNPYMGTQTMRIKVIEGG



PLPFAFDILATSFMYGSRTFIKYPKGIPDFFKQSFPEGFTWERVTRYED



GGVITVMQDTSLEDGCLVYHAQVRGVNFPSNGAVMQKKTKGWEPNTEMM



YPADGGLRGYTHMALKVDGGGHLSCSFVTTYRSKKTVGNIKMPGIHAVD



HRLERLEESDNEMFVVQREHAVAKFCDLPSKLGRL



SEQ ID No. 6 (denoted as mRuby, with peroxisomal

targeting signal):

ATGAATTCACTGATCAAGGAAAATATGCGTATGAAGGTGGTCCTGGAAG



GTTCGGTCAACGGCCACCAATTCAAATGCACAGGTGAAGGAGAAGGCAA



TCCGTACATGGGAACTCAAACCATGAGGATCAAAGTCATCGAGGGAGGA



CCCCTGCCATTTGCCTTTGACATTCTTGCCACGAGCTTCATGTATGGCA



GCCGTACTTTTATCAAGTACCCGAAAGGCATTCCTGATTTCTTTAAACA



GTCCTTTCCTGAGGGTTTTACTTGGGAAAGAGTTACAAGATACGAAGAT



GGTGGAGTCATTACCGTTATGCAGGACACCAGCCTTGAGGATGGCTGTC



TCGTTTACCACGCCCAAGTCAGGGGGGTAAACTTTCCCTCCAATGGTGC



CGTGATGCAGAAGAAGACCAAGGGTTGGGAGCCTAATACAGAGATGATG



TATCCAGCAGATGGTGGTCTGAGGGGATACACTCATATGGCACTGAAAG



TTGATGGTGGTGGCCATCTGTCTTGCTCTTTCGTAACAACTTACAGGTC



AAAAAAGACCGTCGGGAACATCAAGATGCCCGGTATCCATGCCGTTGAT



CACCGCCTGGAAAGGTTAGAGGAAAGTGACAATGAAATGTTCGTAGTAC



AACGCGAACACGCAGTTGCCAAGTTCTGTGACCTTCCATCCAAACTGGG



ACGTCTTTGA