WO2015160690A1 - Protéines fluorescentes photoconvertibles - Google Patents
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- WO2015160690A1 WO2015160690A1 PCT/US2015/025540 US2015025540W WO2015160690A1 WO 2015160690 A1 WO2015160690 A1 WO 2015160690A1 US 2015025540 W US2015025540 W US 2015025540W WO 2015160690 A1 WO2015160690 A1 WO 2015160690A1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
- C07K14/43595—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from coelenteratae, e.g. medusae
Definitions
- the present invention generally relates to fluorescent proteins, for various uses such as for super-resolution microscopy.
- Photoactivatable fluorescent proteins are important probes, for example, for super-resolution microscopy, which allows the spatial organization of proteins in living cells to be probed with sub-diffraction-limit resolution.
- Super-resolution microscopy in general, is defined as optical microscopy at resolutions that exceed the resolution limit set by the diffraction limit of light.
- Recent advances in super-resolution microscopy include stochastic optical reconstruction microscopy (STORM), near-field scanning optical microscopy (NSOM), stimulated emission depletion (STED), ground state depletion microscopy (GSD), reversible saturable optical linear fluorescence transition (RESOLFT), saturated structured-illumination microscopy (SSEVI), and photoactivated localization microscopy (PALM).
- PROM stochastic optical reconstruction microscopy
- NOM near-field scanning optical microscopy
- STED stimulated emission depletion
- GSD ground state depletion microscopy
- RESOLFT reversible saturable optical linear fluor
- the present invention generally relates to fluorescent proteins, for various uses such as for super-resolution microscopy.
- the subject matter of the present invention involves, in some cases, interrelated products, alternative solutions to a particular problem, and/or a plurality of different uses of one or more systems and/or articles.
- the present invention is directed to a composition comprising mMAPLE2. In another set of embodiments, the present invention is directed to a composition comprising mMAPLE3. In another set of embodiments, the present invention is directed to a composition comprising SEQ ID NO: 2. In another set of embodiments, the present invention is directed to a composition comprising positions 2- 237 of SEQ ID NO: 2.
- the present invention is directed to a composition comprising SEQ ID NO: 1 with the provisios that position 111 is any amino acid residue except I and position 198 is any amino acid residue except Y. In another set of embodiments, the present invention is directed to a composition comprising positions 2- 237 of SEQ ID NO: 1 with the provisios that position 111 is any amino acid residue except I and position 198 is any amino acid residue except Y.
- the present invention is directed to a composition comprising positions 17-225 of SEQ ID NO: 2. In another set of embodiments, the present invention is directed to a composition comprising positions 17-225 of SEQ ID NO: 1 with the provisios that position 111 is any amino acid residue except I and position 198 is any amino acid residue except Y.
- the present invention is directed to a composition comprising SEQ ID NO: 3. In another set of embodiments, the present invention is directed to a composition comprising positions 2-237 of SEQ ID NO: 3.
- the present invention is directed to a composition comprising SEQ ID NO: 1 with the provisios that position 82 is any amino acid residue except E, position 83 is any amino acid residue except D, position 111 is any amino acid residue except I, position 197 is any amino acid residue except D, and position 198 is any amino acid residue except Y.
- the present invention is directed to a composition comprising positions 2-237 of SEQ ID NO: 1 with the provisios that position 82 is any amino acid residue except E, position 83 is any amino acid residue except D, position 111 is any amino acid residue except I, position 197 is any amino acid residue except D, and position 198 is any amino acid residue except Y.
- the present invention is directed to a composition comprising positions 17-225 of SEQ ID NO: 3.
- the present invention is generally directed to a nucleic acid, at least a portion of which encodes the amino acid sequence of mMAPLE2. In another set of embodiments, the present invention is generally directed to a nucleic acid, at least a portion of which encodes the amino acid sequence of mMAPLE3. In another set of embodiments, the present invention is generally directed to a nucleic acid, at least a portion of which encodes the amino acid sequence of SEQ ID NO: 2. In another set of embodiments, the present invention is generally directed to a nucleic acid, at least a portion of which encodes positions 2-237 of the amino acid sequence of SEQ ID NO: 2.
- the present invention is generally directed to a nucleic acid, at least a portion of which encodes SEQ ID NO: 1 with the provisios that position 111 is any amino acid residue except I and position 198 is any amino acid residue except Y. In another set of embodiments, the present invention is generally directed to a nucleic acid, at least a portion of which encodes positions 2-237 of SEQ ID NO: 1 with the provisios that position 111 is any amino acid residue except I and position 198 is any amino acid residue except Y.
- the present invention is generally directed to a nucleic acid, at least a portion of which encodes the amino acid sequence of SEQ ID NO: 3. In another set of embodiments, the present invention is generally directed to a nucleic acid, at least a portion of which encodes positions 2-237 of the amino acid sequence of SEQ ID NO: 3.
- the present invention is generally directed to a nucleic acid, at least a portion of which encodes SEQ ID NO: 1 with the provisios that position 82 is any amino acid residue except E, position 83 is any amino acid residue except D, position 111 is any amino acid residue except I, position 197 is any amino acid residue except D, and position 198 is any amino acid residue except Y.
- the present invention is generally directed to a nucleic acid, at least a portion of which encodes positions 2-237 of SEQ ID NO: 1 with the provisios that position 82 is any amino acid residue except E, position 83 is any amino acid residue except D, position 111 is any amino acid residue except I, position 197 is any amino acid residue except D, and position 198 is any amino acid residue except Y.
- the present invention is generally directed to a nucleic acid encoding an amino acid sequence that has a sequence identity of at least about 90% with SEQ ID NO: 2. In another set of embodiments, the present invention is generally directed to a nucleic acid encoding an amino acid sequence that has a sequence identity of at least about 95% with SEQ ID NO: 2. In another set of embodiments, the present invention is generally directed to a nucleic acid encoding an amino acid sequence that has a sequence identity of at least about 90% with SEQ ID NO: 3. In another set of embodiments, the present invention is generally directed to a nucleic acid encoding an amino acid sequence that has a sequence identity of at least about 95% with SEQ ID NO: 3.
- the present invention encompasses methods of making one or more of the embodiments described herein, for example, proteins such as mMAPLE2 and/or mMAPLE3. In still another aspect, the present invention encompasses methods of using one or more of the embodiments described herein, for example, proteins such as mMAPLE2 and/or mMAPLE3.
- Figs. 1A-1D illustrates measurements of certain PAFPs in accordance with one embodiment of the invention
- Figs. 2A-2F illustrates measurements of various PAFPs in accordance with another embodiment of the invention
- Figs. 3A-3D illustrates dimerization of certain PAFPs in yet another embodiment of the invention
- Figs. 4A-4B illustrates signaling efficiency of certain PAFPs in still another embodiment of the invention
- Figs. 5A-5G illustrates certain proteins in accordance with various embodiments of the invention
- Figs. 6A-6D illustrates blinking number distributions of certain PAFPs in another embodiment of the invention
- Figs. 7A-7B illustrates maturation half-life in yet another embodiment of the invention
- Fig. 8 illustrates signaling efficiency versus maturation half-life in still another embodiment of the invention.
- Figs. 9A-9C illustrates excitation and emission spectra in accordance with certain embodiments of the invention.
- SEQ ID NO: 1 is mMAPLE having a sequence:
- SEQ ID NO: 2 is mMAPLE2 having a sequence:
- SEQ ID NO: 3 is mMAPLE3 having a sequence:
- SEQ ID NO: 5 has a sequence SGGGGSK.
- SEQ ID NO: 6 has a sequence CHHHHHHGSG.
- SEQ ID NO: 7 has a sequence GSGHHHHHH.
- the present invention generally relates to fluorescent proteins, for various uses such as for super-resolution microscopy.
- the protein is mMAPLE2 or mMAPLE3.
- the protein comprises two or substitutions in mMAPLE.
- the present invention is generally directed to systems and methods for making or using such proteins, kits involving such proteins, nucleic acids encoding such proteins, vectors or plasmids comprising such proteins or nucleic acids, or cells or organisms comprising such proteins or nucleic acids, as well as fragments, homologs, analogs, derivatives, or functionally equivalent compositions.
- the present invention is generally directed to proteins that are generally related to mMAPLE (SEQ ID NO: 1), such as mMAPLE2 (SEQ ID NO: 2) and mMAPLE3 (SEQ ID NO: 3).
- mMAPLE2 SEQ ID NO: 2
- mMAPLE3 SEQ ID NO: 3
- Other proteins of the invention related to mMAPLE are discussed in more detail below. It should be noted that many of the proteins discussed herein are not naturally- occurring.
- such proteins may be fluorescent, or may be useful of microscopy.
- the proteins may be useful in super-resolution microscopy techniques such as PALM or STORM, or in other techniques including those described herein.
- such proteins may be photoactivatable,
- An entity is "activatable” if it can be activated from a state not capable of emitting light (e.g., at a specific wavelength) to a state capable of emitting light (e.g., at that wavelength).
- the entity may or may not be able to be deactivated, e.g., by using deactivation light or other techniques for deactivating light.
- An entity is "switchable” if it can be switched between two or more different states, one of which is capable of emitting light (e.g., at a specific wavelength). In the other state(s), the entity may emit no light, or emit light at a different wavelength. For instance, an entity can be "activated" to a first state able to produce light having a desired
- the entity is activatable using light, then the entity is a "photoactivatable” entity.
- the entity is switchable using light in combination or not in combination with other techniques, then the entity is a "photo switchable” entity.
- a photo switchable entity may be switched between different light-emitting or non-emitting states by incident light of different wavelengths.
- a "switchable" entity can be identified by one of ordinary skill in the art by determining conditions under which an entity in a first state can emit light when exposed to an excitation wavelength, switching the entity from the first state to the second state, e.g., upon exposure to light of a switching wavelength, then showing that the entity, while in the second state, can no longer emit light (or emits light at a reduced intensity) or emits light at a different wavelength when exposed to the excitation wavelength.
- the switchable entity includes a first, light-emitting portion (e.g,. a fluorophore), and a second portion that activates or "switches" the first portion. For example, upon exposure to light, the second portion of the switchable entity may activate the first portion, causing the first portion to emit light.
- a first, light-emitting portion e.g,. a fluorophore
- the second portion of the switchable entity may activate the first portion, causing the first portion to emit light.
- the entity can be reversibly switched between the two or more states, e.g., upon exposure to the proper stimuli.
- a first stimulus e.g., a first wavelength of light
- a second stimulus e.g., a second wavelength of light or light with the first wavelength
- Any suitable method may be used to activate the entity.
- incident light of a suitable wavelength may be used to activate the entity to be able to emit light, and the entity can then emit light when excited by an excitation light.
- the photo switchable entity can be switched between different light-emitting or non- emitting states by incident light.
- an emissive entity in a sample is an entity such as an activatable entity, a switchable entity, a photoactivatable entity, or a photoswitchable entity. Examples of such entities are discussed herein. In some cases, more than one type of emissive entity may be present in a sample.
- the present invention is generally directed to proteins such as mMAPLE2 or mMAPLE3.
- the protein comprises a sequence SEQ ID NO: 2 or SEQ ID NO: 3.
- the protein may also contain fragments or portions of SEQ ID NO: 2 or SEQ ID NO: 3.
- the starting amino acid (M) may be absent, such that the protein comprises positions 2-237 of SEQ ID NO: 2 or SEQ ID NO: 3.
- one or both of the head and tail fragments of the protein may be removed, e.g., without substantially affecting the structural integrity of the protein.
- positions 1-16 may be removed and/or replaced with other sequences.
- positions 226-237 may be removed and/or replaced with other sequences.
- both may be removed and/or replaced with other sequences (e.g., keeping positions 17-225).
- the present invention is generally directed to a protein that is based on mMAPLE, but contains one or more modifications.
- the protein may have 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 modifications with respect to mMAPLE (SEQ ID NO: 1).
- the protein contains modifications in at least positions 111 and 198 with respect to mMAPLE.
- the protein may also contain modifications in other positions as well.
- the protein may contain modifications in one or more of positions 82, 83, or 197.
- the protein contains modifications at any one or more of positions 82, 83, 111, 197, or 198 of mMAPLE.
- one or more of these modifications is directed to changing an amino acid from one category (i.e., of basic, acidic, polar, or nonpolar amino acid residues) to a different category.
- amino acids facilitate the dimerization of mMAPLE to itself. Accordingly, it is believed that changing the amino acids at one or more of these locations may reduce or inhibit the ability of mMAPLE to dimerize.
- the basic amino acids are H, K, or R.
- the acidic acids are D or E.
- the polar amino acids are S, T, Y, Q, N, C, G.
- the nonpolar amino acids are F, L, I, M, V, P, A, W.
- position 111 and/or position 198 may be altered.
- position 111 may be altered to N, or position 198 may be altered to A.
- mMAPLE i.e., II 1 IN and Y198A
- the resulting protein is mMAPLE2.
- both of these substitutions need not be made, and that other amino acid residues can be used instead (e.g., position 111 may be substituted with any basic, polar, or acidic amino acid residue, and/or position 198 may be substituted with any basic, acidic, or nonpolar amino acid residue).
- positions 82, 83, 111, 197, and 198 may be modified.
- the amino acid residue may independently be altered to an amino acid residue.
- position 82 may be altered to R
- position 83 may be altered to K
- position 111 may be altered to N
- position 197 may be altered to K
- position 198 may be altered to A.
- the amino acid residue may be substituted with an amino acid residue of a different category (i.e., of basic, acidic, polar, or nonpolar amino acid residues).
- position 82 may be substituted with a basic, polar, or nonpolar amino acid;
- position 83 may be substituted with a basic, polar, or nonpolar amino acid
- position 111 may be substituted with a basic, polar, or acidic amino acid
- position 197 may be substituted with a basic, polar, or nonpolar amino acid
- position 198 may be substituted with a basic, acidic, or nonpolar amino acid.
- a protein may comprise positions 2-237 of mMAPLE with one or more of these substitutions; a protein may comprise positions 17- 225 of mMAPLE with one or more of these substitutions, a protein may comprise positions 1-225 or 2-225 of mMAPLE with one or more of these substitutions, a protein may comprise positions 17-237 of mMAPLE with one or more of these substitutions, etc.
- any of these proteins or protein fragments may contain one or more substitutions in positions 82, 83, 111, 197, and 198, as discussed above.
- the present invention is directed to a protein having a sequence having at least 80% sequence identity with either mMAPLE2 or mMAPLE3.
- the protein may have at least 85%, at least 90%, at least 92%, at least
- amino acid is given its ordinary meaning as used in the field of biochemistry.
- a series of isolated amino acids may be connected to form a peptide or a protein by reaction of the -NH 2 of one amino acid with the -COOH of another amino acid to form a peptide bond (-CO-NH-).
- the "natural amino acids,” as used herein, are the 20 amino acids commonly found in nature, typically in the L-isomer, i.e., alanine ("Ala” or “A”), arginine ("Arg” or “R”), asparagine (“Asn” or “N”), aspartic acid (“Asp” or “D”), cysteine (“Cys” or “C”), glutamine ("Gin” or “Q”), glutamic acid (“Glu” or “E”), glycine (“Gly” or “G”), histidine (“His” or “H”), isoleucine ("He” or “I”), leucine (“Leu” or “L”), lysine ("Lys” or “K”), methionine ("Met” or “M”), phenylalaine (“Phe” or “F”), proline (“Pro” or “P”), serine (“Ser” or “S”), threonine ("Thr” or “T”), tryptophan
- an amino acid that can be either asparagine or aspartic acid is referred to as "Asx" or "B," while an amino acid that can be either glutamine or glutamic acid is referred to as "Glx” or "Z.”
- Some amino acids are basic, e.g., H, K, or R.
- Some amino acids are acidic, e.g., D or E.
- Some amino acids are polar, e.g., S, T, Y, Q, N, C, G.
- Some amino acids are nonpolar, e.g., F, L, I, M, V, P, A, W.
- the present invention is generally directed to nucleic acids encoding any of the proteins described above, or elsewhere herein.
- nucleic acids may be, for example, DNA, cDNA, RNA, etc.
- the nucleic acid may be present as an isolated nucleic acid, or the nucleic acid may be incorporated into a cell, e.g., to produce the corresponding protein.
- the nucleic acid may be one that can be transfected into a cell.
- the nucleic acid is present in a vector or a plasmid.
- proteins and nucleic acids such as those discussed herein may be produced using standard molecular biology methods generally known to those of ordinary skill in the art (see, e.g., Green and Sambrook, Molecular Cloning, A Laboratory Manual, 2012, Cold Spring Harbor Press).
- a nucleic acid may be included within a vector.
- a vector is a nucleic acid (e.g., DNA or cDNA) used as a vehicle to artificially carry genetic material (e.g., an engineered nucleic acid) into another cell where, for example, it can be replicated and/or expressed.
- a vector is an episomal vector (see, e.g., Van Craenenbroeck K. et al. Eur. J. Biochem. 261, 5665, 2000, incorporated by reference herein).
- a non-limiting example of a vector is a plasmid. Plasmids are double- stranded generally circular DNA sequences that are capable of automatically replicating in a host cell.
- Plasmid vectors typically contain an origin of replication that allows for semi-independent replication of the plasmid in the host and also the transgene insert. Plasmids may have more features, including, for example, a "multiple cloning site," which includes nucleotide overhangs for insertion of a nucleic acid insert, and multiple restriction enzyme consensus sites to either side of the insert.
- a vector is a viral vector.
- Nucleic acids as discussed herein may comprise, in some embodiments, promoters operably linked to a nucleotide sequence.
- a "promoter” is a control region of a nucleic acid at which initiation and rate of transcription of the remainder of a nucleic acid are controlled.
- a promoter may also contain sub-regions at which regulatory proteins and molecules may bind, such as RNA polymerase and other transcription factors. Promoters may be constitutive, inducible, activatable, repressible, tissue-specific or any combination thereof.
- a nucleic acid sequence may be positioned under the control of a recombinant or heterologous promoter, which refers to a promoter that is not normally associated with the nucleotide sequence in its natural environment.
- promoters may include promoters of other genes; promoters isolated from any other prokaryotic cell; and synthetic promoters that are not "naturally occurring" such as, for example, those that contain different elements of different transcriptional regulatory regions and/or mutations that alter expression through methods of genetic engineering that are known in the art.
- sequences may be produced using recombinant cloning and/or nucleic acid amplification technology, including polymerase chain reaction (PCR).
- PCR polymerase chain reaction
- a promoter may drive expression or drive transcription of the nucleic acid sequence that it regulates.
- a promoter is considered to be "operably linked" when it is in a correct functional location and orientation in relation to the nucleotide sequence it regulates to control (“drive”) transcriptional initiation and/or expression of that sequence.
- a promoter may be classified in some cases as strong or weak according to its affinity for RNA polymerase (and/or sigma factor); this is related to how closely the promoter sequence resembles the ideal consensus sequence for the polymerase.
- the strength of a promoter may depend on whether initiation of transcription occurs at that promoter with high or low frequency. Different promoters with different strengths may be used to construct nucleic acids with different levels of gene/protein expression (e.g., the level of expression initiated from a weak promoter is lower than the level of expression initiated from a strong promoter).
- a nucleic acid may be codon- optimized, for example, for expression in human cells or other types of cells, such as E. coli. Codon optimization is a technique to maximize the protein expression in living organism by increasing the translational efficiency of gene of interest by transforming a DNA sequence of nucleotides of one species into a DNA sequence of nucleotides of another species.
- engineered constructs are expressed in mammalian cells.
- engineered constructs are expressed in human cells, primate cells (e.g., vero cells), rat cells (e.g., GH3 cells, OC23 cells) or mouse cells (e.g., MC3T3 cells).
- HEK cells there are a variety of human cell lines, including, without limitation, HEK cells, HeLa cells, cancer cells from the National Cancer Institute's 60 cancer cell lines (NCI60), DU145 (prostate cancer) cells, Lncap (prostate cancer) cells, MCF-7 (breast cancer) cells, MDA-MB-438 (breast cancer) cells, PC3 (prostate cancer) cells, T47D (breast cancer) cells, THP-1 (acute myeloid leukemia) cells, U87 (glioblastoma) cells, SHSY5Y human neuroblastoma cells (cloned from a myeloma) and Saos-2 (bone cancer) cells.
- engineered constructs are expressed in human embryonic kidney (HEK) cells (e.g., HEK 293 or HEK 293T cells).
- HEK human embryonic kidney
- engineered constructs are expressed in bacterial cells, yeast cells, insect cells or other types of cells.
- a modified cell is a cell that contains an exogenous nucleic acid or a nucleic acid that does not occur in nature, such as those nucleic acids described herein.
- a modified cell contains an independently replicating nucleic acid (e.g., an engineered nucleic acid present on an episomal vector).
- a modified cell is produced by introducing a foreign or exogenous nucleic acid into a cell.
- a nucleic acid may be introduced into a cell by conventional methods, such as, for example, electroporation (see, e.g., Heiser
- a cell is modified to overexpress a protein of interest (e.g. , via introducing or modifying a promoter or other regulatory element near the
- a cell is modified by mutagenesis.
- a cell is modified by introducing a recombinant nucleic acid into the cell in order to produce a genetic change of interest (e.g. , via insertion or homologous recombination).
- suitable techniques to cause a cell to produce a protein of interest e.g., through overexpression or other well-known techniques.
- the cell may be the cell of an organism, e.g., a human or a non-human mammal, a bacterial cell (e.g., E. coli), or the like.
- Nucleic acids such as those discussed herein may be transiently expressed or stably expressed in various embodiments.
- Transient cell expression refers to expression by a cell of a nucleic acid that is not integrated into the nuclear genome of the cell.
- stable cell expression refers to expression by a cell of a nucleic acid that remains in the nuclear genome of the cell and its daughter cells.
- a cell is co-transfected with a marker gene and an exogenous nucleic acid (e.g. , engineered nucleic acid) that is intended for stable expression in the cell.
- the marker gene gives the cell some selectable advantage (e.g., resistance to a toxin, antibiotic, or other factor).
- marker genes and selection agents for use in accordance with the present disclosure include, without limitation, dihydrofolate reductase with methotrexate, glutamine synthetase with methionine sulphoximine, hygromycin phosphotransferase with hygromycin, puromycin N- acetyltransferase with puromycin, and neomycin phosphotransferase with Geneticin, also known as G418.
- Other marker genes/selection agents known to those of ordinary skill in the art are also contemplated in other embodiments.
- Expression of nucleic acids in transiently-transfected and/or stably-transfected cells may be constitutive or inducible. Inducible promoters for use as provided herein are described above.
- Mammalian cells modified to comprise a nucleic acid as discussed herein may be cultured (e.g., maintained in cell culture) using conventional mammalian cell culture methods known to those of ordinary skill in the art (see, e.g., Phelan M.C. Curr Protoc Cell Biol. 2007 Sep; Chapter 1: Unit 1.1, incorporated by reference herein).
- cells may be grown and maintained at an appropriate temperature and gas mixture (e.g., 37 °C, 5% C0 2 for mammalian cells) in a cell incubator. Culture conditions may vary for each cell type.
- cell growth media may vary in pH, glucose concentration, growth factors, and the presence of other nutrients.
- Growth factors used to supplement media are often derived from the serum of animal blood, such as fetal bovine serum (FBS), bovine calf serum, equine serum and/or porcine serum.
- FBS fetal bovine serum
- bovine calf serum bovine calf serum
- equine serum equine serum
- porcine serum equine serum
- culture media used as provided herein may be commercially available and/or well-described (see, e.g., Birch J. R., R.G. Spier (Ed.) Encyclopedia of Cell Technology, Wiley. 411-424, 2000; Keen M. J.
- images of a sample may be obtained using stochastic imaging techniques.
- stochastic imaging techniques various entities are activated and emit light at different times and imaged; typically the entities are activated in a random or "stochastic" manner.
- a statistical or "stochastic" subset of the entities within a sample can be activated from a state not capable of emitting light at a specific wavelength to a state capable of emitting light at that wavelength.
- Some or all of the activated entities may be imaged (e.g., upon excitation of the activated entities), and this process repeated, each time activating another statistical or "stochastic" subset of the entities.
- the entities are deactivated (for example, spontaneously, or by causing the deactivation, for instance, with suitable deactivation light). Repeating this process any suitable number of times allows an image of the sample to be built up using the statistical or "stochastic" subset of the activated emissive entities activated each time. Higher resolutions may be achieved in some cases because the emissive entities are not all simultaneously activated, making it easier to resolve closely positioned emissive entities.
- Non-limiting examples of stochastic imaging techniques include stochastic optical reconstruction microscopy (STORM), single-molecule localization microscopy (SMLM), spectral precision distance microscopy (SPDM), super-resolution optical fluctuation imaging (SOFI), photoactivated localization microscopy (PALM), and fluorescence
- FPALM photoactivation localization microscopy
- the term "light” generally refers to electromagnetic radiation, having any suitable wavelength (or equivalently, frequency).
- the light may include wavelengths in the optical or visual range (for example, having a wavelength of between about 380 nm and about 750 nm, i.e., "visible light"), infrared wavelengths (for example, having a wavelength of between about 700 micrometers and 1000 nm), ultraviolet wavelengths (for example, having a wavelength of between about 400 nm and about 10 nm), or the like.
- more than one type of entity may be used, e.g., entities that are chemically different or distinct, for example, structurally. However, in other cases, the entities are chemically identical or at least substantially chemically identical.
- the resolution of the entities in the images can be, for instance, on the order of 1 micrometer or less, as described herein.
- the resolution of an entity may be determined to be less than the wavelength of the light emitted by the entity, and in some cases, less than half the wavelength of the light emitted by the entity. For example, if the emitted light is visible light, the resolution may be determined to be less than about 700 nm.
- two (or more) entities can be resolved even if separated by a distance of less than about 500 nm, less than about 300 nm, less than about 200 nm, less than about 100 nm, less than about 80 nm, less than about 60 nm, less than about 50 nm, or less than about 40 nm. In some cases, two or more entities separated by a distance of less than about 35 nm, less than about 30 nm, less than about 25 nm, less than about 20 nm, less than about 15 nm, less than about 10 nm, or less than about 5 nm can be resolved using embodiments of the present invention.
- STORM stochastic optical reconstruction microscopy
- incident light is applied to emissive entities within a sample in a sample region to activate the entities, where the incident light has an intensity and/or frequency that is able to cause a statistical subset of the plurality of emissive entities to become activated from a state not capable of emitting light (e.g., at a specific wavelength) to a state capable of emitting light (e.g., at that wavelength).
- the emissive entities may spontaneously emit light, and/or excitation light may be applied to the activated emissive entities to cause these entities to emit light.
- the excitation light may be of the same or different wavelength as the activation light.
- the emitted light can be collected or acquired, e.g., in one, two, or more objectives as previously discussed. In certain embodiments the positions of the entities can be determined in two or three dimensions from their images.
- the excitation light is also able to subsequently deactivate the statistical subset of the plurality of emissive entities, and/or the entities may be deactivated via other suitable techniques (e.g., by applying deactivation light, by applying heat, by waiting a suitable period of time, etc.).
- a stochastic image of some or all of the emissive entities within a sample may be produced, e.g., from the determined positions of the entities.
- various image processing techniques such as noise reduction and/or x, y and/or z position determination can be performed on the acquired images.
- incident light having a sufficiently weak intensity may be applied to a plurality of entities such that only a subset or fraction of the entities within the incident light are activated, e.g., on a stochastic or random basis.
- the amount of activation can be any suitable fraction, e.g., less than about 0.01%, less than about 0.03%, less than about 0.05%, less than about 0.1%, less than about 0.3%, less than about 0.5%, less than about 1%, less than about 3%, less than about 5%, less than about 10%, less than less than about 15%, less than about 20%, less than about 25%, less than about 30%, less than about 35%, less than about 40%, less than about 45%, less than about 50%, less than about 55%, less than about 60%, less than about 65%, less than about 70%, less than about 75%, less than about 80%, less than about 85%, less than about 90%, or less than about 95% of the entities may be activated, depending on the application.
- a sparse subset of the entities may be activated such that at least some of them are optically resolvable from each other and their positions can be determined.
- the activation of the subset of the entities can be synchronized by applying a short duration of incident light. Iterative activation cycles may allow the positions of all of the entities, or a substantial fraction of the entities, to be determined. In some cases, an image with sub-diffraction limit resolution can be constructed using this information.
- a sample may contain a plurality of various entities, some of which are at distances of separation that are less than the wavelength of the light emitted by the entities or below the diffraction limit of the emitted light. Different locations within the sample may be determined (e.g., as different pixels within an image), and each of those locations independently analyzed to determine the entity or entities present within those locations. In some cases, the entities within each location are determined to resolutions that are less than the wavelength of the light emitted by the entities or below the diffraction limit of the emitted light, as previously discussed.
- the activation light and deactivation light have the same wavelength. In some cases, the activation light and deactivation light have different wavelengths. In some cases, the activation light and excitation light have the same wavelength. In some cases, the activation light and excitation light have different wavelengths. In some cases, the excitation light and deactivation light have the same wavelength. In some cases, the excitation light and deactivation light have different wavelengths. In some cases, the activation light, excitation light and deactivation light all have the same wavelength.
- the light may be monochromatic (e.g., produced using a laser) or polychromatic.
- the entity may be activated upon stimulation by electric fields and/or magnetic fields.
- the entity may be activated upon exposure to a suitable chemical environment, e.g., by adjusting the pH, or inducing a reversible chemical reaction involving the entity, etc.
- any suitable method may be used to deactivate the entity, and the methods of activating and deactivating the entity need not be the same. For instance, the entity may be deactivated upon exposure to incident light of a suitable wavelength, or the entity may be deactivated by waiting a sufficient time.
- the switchable entity can be immobilized, e.g., covalently, with respect to a binding partner, i.e., a molecule that can undergo binding with a particular analyte.
- binding partners include specific, semi- specific, and nonspecific binding partners as known to those of ordinary skill in the art.
- binding partner e.g., protein, nucleic acid, antibody, etc.
- a binding partner refers to a reaction that is determinative of the presence and/or identity of one or other member of the binding pair in a mixture of heterogeneous molecules (e.g., proteins and other biologies).
- the ligand would specifically and/or preferentially select its receptor from a complex mixture of molecules, or vice versa.
- Other examples include, but are not limited to, an enzyme would specifically bind to its substrate, a nucleic acid would specifically bind to its complement, an antibody would specifically bind to its antigen.
- the binding may be by one or more of a variety of mechanisms including, but not limited to ionic interactions, and/or covalent interactions, and/or hydrophobic
- the switchable entity By immobilizing a switchable entity with respect to the binding partner of a target molecule or structure (e.g., DNA or a protein within a cell), the switchable entity can be used for various determination or imaging purposes.
- a switchable entity having an amine-reactive group may be reacted with a binding partner comprising amines, for example, antibodies, proteins or enzymes.
- more than one switchable entity may be used, and the entities may be the same or different.
- the light emitted by a first entity and the light emitted by a second entity have the same wavelength.
- the entities may be activated at different times and the light from each entity may be determined separately. This allows the location of the two entities to be determined separately and, in some cases, the two entities may be spatially resolved, even at distances of separation that are less than the wavelength of the light emitted by the entities or below the diffraction limit of the emitted light (i.e., "sub-diffraction limit" resolutions).
- the light emitted by a first entity and the light emitted by a second entity have different wavelengths (for example, if the first entity and the second entity are chemically different, and/or are located in different environments).
- the entities may be spatially resolved even at distances of separation that are less than the wavelength of the light emitted by the entities or below the diffraction limit of the emitted light.
- the light emitted by a first entity and the light emitted by a second entity have substantially the same wavelengths, but the two entities may be activated by light of different wavelengths and the light from each entity may be determined separately.
- the entities may be spatially resolved even at distances of separation that are less than the wavelength of the light emitted by the entities, or below the diffraction limit of the emitted light.
- the entities may be independently switchable, i.e., the first entity may be activated to emit light without activating a second entity.
- the methods of activating each of the first and second entities may be different (e.g., the entities may each be activated using incident light of different wavelengths).
- a sufficiently weak intensity of light may be applied to the entities such that only a subset or fraction of the entities within the incident light are activated, i.e., on a stochastic or random basis. Specific intensities for activation can be determined by those of ordinary skill in the art using no more than routine skill.
- the first entity may be activated without activating the second entity.
- the entities may be spatially resolved even at distances of separation that are less than the wavelength of the light emitted by the entities, or below the diffraction limit of the emitted light.
- the sample to be imaged may comprise a plurality of entities, some of which are substantially identical and some of which are substantially different. In this case, one or more of the above methods may be applied to independently switch the entities.
- the entities may be spatially resolved even at distances of separation that are less than the wavelength of the light emitted by the entities, or below the diffraction limit of the emitted light.
- incident light having a sufficiently weak intensity may be applied to a plurality of entities such that only a subset or fraction of the entities within the incident light are activated, e.g., on a stochastic or random basis.
- the amount of activation may be any suitable fraction, e.g., about 0.1%, about 0.3%, about 0.5%, about 1%, about 3%, about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% of the entities may be activated, depending on the application.
- a sparse subset of the entities may be activated such that at least some of them are optically resolvable from each other and their positions can be determined.
- the activation of the subset of the entities can be synchronized by applying a short duration of the incident light. Iterative activation cycles may allow the positions of all of the entities, or a substantial fraction of the entities, to be determined. In some cases, an image with sub-diffraction limit resolution can be constructed using this information.
- a microscope may be configured so to collect light emitted by the switchable entities while minimizing light from other sources of fluorescence (e.g., "background noise").
- imaging geometry such as, but not limited to, a total-internal-reflection geometry, a spinning-disc confocal geometry, a scanning confocal geometry, an epi-fluorescence geometry, an epi-fluorescence geometry with an oblique incidence angle, etc., may be used for sample excitation.
- a thin layer or plane of the sample is exposed to excitation light, which may reduce excitation of fluorescence outside of the sample plane.
- a high numerical aperture lens may be used to gather the light emitted by the sample.
- the light may be processed, for example, using filters to remove excitation light, resulting in the collection of emission light from the sample.
- the magnification factor at which the image is collected can be optimized, for example, when the edge length of each pixel of the image corresponds to the length of a standard deviation of a diffraction limited spot in the image.
- the switchable entities may also be resolved as a function of time. For example, two or more entities may be observed at various time points to determine a time-varying process, for example, a chemical reaction, cell behavior, binding of a protein or enzyme, etc.
- the positions of two or more entities may be determined at a first point of time (e.g., as described herein), and at any number of subsequent points of time.
- the common entity may then be determined as a function of time, for example, time-varying processes such as movement of the common entity, structural and/or configurational changes of the common entity, reactions involving the common entity, or the like.
- the time-resolved imaging may be facilitated in some cases since a switchable entity can be switched for multiple cycles, with each cycle giving one data point of the position of the entity.
- one or more light sources may be time-modulated (e.g., by shutters, acoustic optical modulators, or the like).
- a light source may be one that is activatable and deactivatable in a programmed or a periodic fashion.
- more than one light source may be used, e.g., which may be used to illuminate a sample with different wavelengths or colors.
- the light sources may emanate light at different frequencies, and/or color-filtering devices, such as optical filters or the like, may be used to modify light coming from the light sources such that different wavelengths or colors illuminate a sample.
- drift correction or noise filters may be used.
- a fixed point is identified (for instance, as a fiduciary marker, e.g., a fluorescent particle may be immobilized to a substrate), and movements of the fixed point (i.e., due to mechanical drift) are used to correct the determined positions of the switchable entities.
- the correlation function between images acquired in different imaging frames or activation frames can be calculated and used for drift correction.
- the drift may be less than about 1000 nm/min, less than about 500 nm/min, less than about 300 nm/min, less than about 100 nm/min, less than about 50 nm/min, less than about 30 nm/min, less than about 20 nm/min, less than about 10 nm/min, or less than 5 nm/min.
- Such drift may be achieved, for example, in a microscope having a translation stage mounted for x-y positioning of the sample slide with respect to the microscope objective.
- the slide may be immobilized with respect to the translation stage using a suitable restraining mechanism, for example, spring loaded clips.
- a buffer layer may be mounted between the stage and the microscope slide. The buffer layer may further restrain drift of the slide with respect to the translation stage, for example, by preventing slippage of the slide in some fashion.
- the buffer layer in one embodiment, is a rubber or polymeric film, for instance, a silicone rubber film.
- one embodiment of the invention is directed to a device comprising a translation stage, a restraining mechanism (e.g., a spring loaded clip) attached to the translation stage able to immobilize a slide, and optionally, a buffer layer (e.g., a silicone rubber film) positioned such that a slide restrained by the restraining mechanism contacts the buffer layer.
- a "focus lock" device may be used in some cases.
- a laser beam may be reflected from the substrate holding the sample and the reflected light may be directed onto a position-sensitive detector, for example, a quadrant photodiode.
- the position of the reflected laser which may be sensitive to the distance between the substrate and the objective, may be fed back to a z-positioning stage, for example a piezoelectric stage, to correct for focus drift.
- the device may also include, for example, a spatial light modulator and/or a polarizer, e.g., as discussed herein.
- a computer and/or an automated system may be provided that is able to automatically and/or repetitively perform any of the methods described herein.
- a computer may be used to control excitation of the switchable entities and the acquisition of images of the switchable entities.
- a sample may be excited using light having various wavelengths and/or intensities, and the sequence of the wavelengths of light used to excite the sample may be correlated, using a computer, to the images acquired of the sample containing the switchable entities.
- the computer may apply light having various wavelengths and/or intensities to a sample to yield different average numbers of activated switchable elements in each region of interest (e.g., one activated entity per location, two activated entities per location, etc.).
- this information may be used to construct an image of the switchable entities, in some cases at sub-diffraction limit resolutions, as noted above.
- the system may include a microscope, a device for activating and/or switching the entities to produce light having a desired wavelength (e.g., a laser or other light source), a device for determining the light emitted by the entities (e.g., a camera, which may include color- filtering devices, such as optical filters), and a computer for determining the spatial positions of the two or more entities.
- a desired wavelength e.g., a laser or other light source
- a device for determining the light emitted by the entities e.g., a camera, which may include color- filtering devices, such as optical filters
- a computer for determining the spatial positions of the two or more entities.
- the systems and methods described herein may also be combined with other imaging techniques known to those of ordinary skill in the art, such as high-resolution fluorescence in situ hybridization (FISH) or immunofluorescence imaging, live cell imaging, confocal imaging, epi-fluorescence imaging, total internal reflection fluorescence imaging, etc.
- FISH fluorescence in situ hybridization
- an existing microscope e.g., a commercially- available microscope
- components such as discussed herein, e.g., to acquire images and/or to determine the positions of emissive entities, as discussed herein.
- PAFPs Photoactivatable fluorescent proteins
- properties of PAFPs may influence the quality of the super- solution images. These properties include (i) the number of photons emitted per switching cycle, which affects the localization precision of individual molecules, (ii) the ratio of the on- and off- switching rate constants, which limits the achievable localization density, (iii) the dimerization tendency, which could cause undesired aggregation of target proteins, and (iv) the signaling efficiency, which determines the fraction of target-PAFP fusion proteins that is detectable in a cell. In this example, these properties were evaluated for twelve commonly used PAFPs.
- reconstruction microscopy and related imaging methods take advantage of photo switching and imaging of single molecules to circumvent the diffraction limit of spatial resolution in light microscopy.
- PRM reconstruction microscopy
- only a subset of the fluorescent labels in the sample is switched on at any given time such that the positions of individual fluorophores can be localized from their images with high precision. Iteration of this process allows numerous fluorescent labels to be localized and an image with sub- diffraction-limit resolution to be reconstructed from the fluorophore localizations.
- Fluorescent proteins that can be activated from dark to fluorescent or converted from one color to another are widely used for such imaging approaches.
- photoactivatable fluorescent proteins PAFPs
- PAFPs photoactivatable fluorescent proteins
- the photon budget defined as the average number of photons emitted in each switching event. Given that the error of localizing an individual fluorophore approximately scales with the inverse square root of the number of detected photons, a higher photon budget may lead to higher localization precision and hence higher image resolution, ii) The on- off switching rate ratio (on-off ratio), defined as the ratio between the on-switching (activation) and off- switching or photobleaching rates under the illumination of the imaging light only. Even in the absence of activation light, the imaging light itself can also switching on the PAFPs, albeit at a low rate.
- the ratio between the on- switching and off- switching rates under this condition determines the lower bound of the fraction of PAFP molecules in the on state at any given time.
- the presence of activation light would increase this fraction.
- the product of this fraction and the density of fluorescent labels reaches ⁇ 1 fluorophore per diffraction-limited volume, it becomes difficult to resolve and precisely localize the activated fluorophores.
- the on-off ratio limits the density of fluorescent labels that can be localized, which in turn affects the effective image resolution based on the Nyquist sampling theorem, iii) The dimerization tendency.
- Many PAFPs have a weak tendency to form dimers, this could even be true for the PAFP that are reported as being monomeric.
- the signaling efficiency defined as the ratio between the number of detectable PAFP-fusion molecules per cell and the expression level of the fusion protein. Fluorescent proteins do not necessarily fold with 100% efficiency. Among the folded molecules, not all of them will become mature at the time of imaging. Among the matured PAFP molecules, only a subset can be photoactivated and imaged. Because of these deficiencies, the number of fusion molecules detected could be substantially lower than the expression level of the fusion protein. PAFPs with higher signaling efficiencies will lead to higher localization densities for a given target protein, which will in turn increase the effective image resolution.
- This example measured the above properties of twelve commonly used PAFPs, including PAGFP, Dendra2, mEos2, mEos3.2, tdEos, mKikGR, PAmCherry, PAtagRFP, mMaple, PSCFP2, Dronpa, and mGeosM. From this screen, it was found that none of these PAFPs was optimal in all four criteria described above. For example, PAtagRFP and mEos3.2 exhibited the highest photon budgets among PAFPs, excellent on-off ratios, and undetectable dimerization tendencies, but showed poor signaling efficiencies.
- mMaple provided excellent signaling efficiency and on-off ratio with a photon budget nearly equal to those of PAtagRFP and mEos3.2, but had a substantial dimerization tendency.
- two new PAFPs were developed in this example based on mMaple that exhibited substantially reduced or undetectable dimerization tendencies while maintaining the high signaling efficiency, high photon budget and low on-off ratio of mMaple. These new PAFPs may substantially facilitate super-resolution imaging of cellular structures.
- Photon budget of photoactivatable fluorescent proteins To evaluate the properties of PAFPs under conditions similar to typical super-resolution imaging experiments, each PAFP was fused to various target proteins and expressed these fusion proteins in either mammalian cells or bacteria. In order to measure the photon budget, the PAFPs were fused to the mammalian focal adhesion protein Zyxin, transiently transfected BS-C-1 cells with the fusion constructs, and imaged the cells using the super- resolution imaging mode in which individual activated proteins were imaged. The distributions of the photon numbers detected per activation event were determined for all twelve PAFPs. Four example distributions, for mEos3.2, mMaple, PSCFP2 and PAGFP, are shown in Fig. 1. The mean photon numbers determined from these distributions are listed in Table 1.
- FIG. 1A Photon number measurements of PAFPs.
- the histograms are example photon number distributions of mEos3.2 (Fig. 1A), mMaple (Fig. IB), PSCFP2 (Fig. 1C), and PAGFP (Fig. ID) measured by imaging individual Zyxin-PAFP fusion proteins in live BS-C-1 cells. The mean photon numbers are indicated.
- rsFastLime and rsEGFP were also imaged. Both of these proteins gave relatively low photon budget ( ⁇ 60 photons per switching event), which would lead to relatively poor localization precision. It is, however, worth noting that these proteins are excellent choices for a different mode of super-resolution imaging (RESOLFT) due to the large number of switching cycles that they exhibit before photobleaching.
- RESOLFT super-resolution imaging
- On-off ratio of photoactivatable fluorescent proteins To determine the on-off ratio, the rates for switching on and switching off (or photobleaching) the PAFPs were measured in the presence of imaging light only. By definition, the on-switching rate is the increment in probability of the on-switching events per unit time. To measure this quantity, the Zyxin-PAFP expressing cells were imaged in the super-resolution mode for a short period of time without any activation light (with imaging light only). The samples were then imaged to completion with an additional activation light at 405 nm. The ratio of the total number of activation events accumulated by a certain time during the period without activation light over the total number of activation events by the end of the imaging process was determined.
- the slope of this cumulative activation probability against time then gave the on-switching rate (Fig. 2A, B, Table 2).
- the off-switching rate was determined from the inverse of the mean lifetime of the on state of each PAFP in the presence of the imaging light (Fig. 2C, D, Table 2).
- the ratios between the on- and off- switching rates were determined for all twelve PAFPs (Table 1). Because both on- and off-switching rates scale linearly with the illumination intensity, the on-off ratio should be independent of the light intensity.
- the on-off ratios were generally very small (10 ⁇ 5 - 10 "6 ) except for PAGFP, Dronpa and mGeosM, which were -10 " .
- On-switching rate and mean lifetime of PAFPs were measured live BS-C-1 cells transiently transfected with zyxin::PAFP plasmids. Each frame corresponds to 16 ms.
- Dimerization tendency of photoactivatable fluorescent proteins Dimerization or oligomerization of fluorescent proteins may cause undesired aggregation of the target proteins.
- the fluorescent proteins are fused to the E. coli protease ClpP, which itself oligomerizes to form a tetradecameric complex. It has been suggested that ClpP proteins tend to aggregate and form a single visible punctum in E.
- E. coli codon- optimized PAFP sequences were fused to the chromosomal copy of clpP, and it was reported whether cells exhibit the single-punctum phenotype (Table 1, Fig. 3A). Fusion with mKikGR, mGeosM, mMaple, PAmCherry, PSCFP2, or mEos2 all led ClpP to form a single punctum in at least a subset of cells, suggesting that these PAFPs exhibit appreciable dimerization tendency, whereas
- FIG. 2A-2B Cumulative on-switching probability as a function of time without activation light. The slope of the line gives the on-switching rate.
- FIGs. 2C-2D Distribution of the on-state lifetime. Bars represent measured data, which were fitted with a binned exponential
- E. coli nucleoid-associated protein H-NS E. coli chemotactic receptor Tar
- mammalian intermediate filament protein Vimentin fused to different PAFPs.
- H-NS appears as a few large and discrete clusters in cells when fused to mEos2, a previously reported monomeric version of the Eos fluorescent protein. Similar results were observed when H-NS was fused to another reported monomeric PAFP,
- H-NS Given the residual dimerization tendency of mEos2 and PAmCherry detected by the ClpP assay (Fig. 3A), the study of H-NS using other PAFPs was extended. Notably, H-NS generally appeared as large and discrete clusters in cells when fused to PAFPs with appreciable dimerization tendency detected by the ClpP assay, such as mEos2, PAmCherry and mMaple. H-NS also appeared as large clusters when fused to tdEos, even though tdEos did not show sufficient dimerization to drive ClpP aggregation.
- Vimentin filaments were cluster into thick bundles in mammalian cells, whereas Vimentin-mEos3.2 appeared as thin filaments that were similar to immunofluorescence images of Vimentin in untransfected cells (Fig 3D).
- FIG. 3A Phase contrast (left) and conventional fluorescent images (right) of live E. coli cells expressing ClpP-PAFP fusions. PAFPs with substantial dimerization tendencies (mEos2, mMaple) result in the formation of ClpP puncta. PAFPs with little to no dimerization tendencies (mEos3.2, PAtagRFP) produce a diffusive ClpP distribution.
- FIG. 3B Overlaid super-resolution and phase contrast (gray) images of live E. coli cells expressing H-NS-PAFP fusions.
- FIG. 3C Overlaid super-resolution and phase contrast images of fixed E.
- FIG. 3D Super-resolution images of fixed Cos-7 cells expressing Vimentin-PAFP fusions or fixed untransfected Cos-7 cells with immunofluorescent labeling of Vimentin (IM).
- Scale bars: 1000 nm. Signaling efficiency of photoactivatable fluorescent proteins. Even when the PAFP is fused to the target protein at its endogenous chromosomal locus, the number of detectable fluorescent proteins does not necessarily reflect the expression level of the fusion protein. This deficiency not only prevents quantitative analysis of the target protein, but may also reduce the resolution of the image by effectively decreasing the labeling density.
- the relative signaling efficiency of different PAFPs was compared by determining the number of single-molecule localizations per cell of the PAFPs fused to a common target protein under endogenous expression, the PAFPs were fused to the E. coli gene hupA, which encodes a subunit of the nucleoid-associated protein HU, at its endogenous chromosomal locus and determined the total number of HU-PAFP localizations per cell (Fig. 4 and Table 1).
- the four green PAFPs were too dim to be detected as single molecules in E. coli, while the eight red PAFPs showed similar photon budget to those measured in mammalian cells (data not shown).
- mMaple provided by far the largest number of HU localizations, which was 6 - 32 fold higher than those of other HU-PAFP fusion proteins (Fig. 4).
- FIG. 4A Super- resolution images of live E. coli cells expressing HU-PAFP fusions overlaid with phase contrast images (gray). Super-resolution images were acquired till all the PAFP molecules in the field of view were bleached.
- Fig. 4B Numbers of observed localizations per cell for different HU-PAFP fusions. (Error bars represent standard errors of the means).
- the difference in the number of HU-PAFP localizations for different PAFPs may be attributed to multiple reasons.
- One of the possible reasons could be the difference in the number of blinking (switching) events per fluorophore.
- the average number of blinking events were measured in fixed HU-PAFP expressing cells (Table 3).
- the average number of blinking events spanned only a small range from 1.7 to 3.3, which are similar to the results derived from purified PAFP in vitro (Fig. 6).
- the localization numbers divided by the average numbers of blinking events yielded the numbers of imaged molecules per cell (Table 3), which is still much bigger in the case of HU- mMaple expressing cells (4 - 36 fold higher than in other HU-PAFP expressing cells).
- FIG. 6 Blinking number distributions of mEos2, mMaple, mMaple2 and mMaple3 from in vitro measurements.
- the percentages of mEos2, mMaple, mMaple2 and mMaple3 that exhibit more than 1 emission bursts are 56%, 57%, 61%, and 60% respectively.
- the average numbers of blinking (burst) events of the mEos2, mMaple, mMaple2 and mMaple3 molecules are 2.9, 2.8, 3.3 and 3.1, respectively.
- mMaple gives the highest signaling efficiency of 20%.
- the 20% value is roughly consistent with the observations that -60% maturable mMaple have matured under the imaging conditions in E. coli, -70% of mature mMaple can be converted from the green form to the red form, and -80% of the converted molecules are bright enough to be localized by the analysis software. Based on the above observations, approximately one third of mMaple molecules are expected to be localized. The left-over discrepancy could be due to that not all PAFPs are folded into the fluorescent conformation.
- Fig. 7A or HU-mMaple (Fig. 7B) were immobilized on a coverslip and treated with kanamycin to inhibit protein synthesis. Further increase in cellular fluorescence was caused by maturation of existing fluorophores. The average fluorescence per cell pixel was plotted as a function of time (dots) and fit to an exponential curve (black line) to get the maturation half-life.
- Figure 8 PAFP signaling efficiency versus maturation half-life.
- the numbers of imaged molecules per cell after adjustment for the number of blinking events per molecule are plotted against the maturation half-lives.
- the numbers of molecules in the figure are from E. coli cells grown at 32 °C to match the temperature used for maturation half-life measurements. As a result the numbers are different from those reported in
- the black line indicates the expected number of observable molecules at each half-life value if the maturation time of the fluorophore is the only variable causing the difference in the signaling efficiency. This line was derived from the number of imaged mMaple molecules and Eq. 5 (see below), assuming equal expression rate. The discrepancy between the line and the measured dots shows that the difference in maturation half-life cannot fully account for the difference in signaling efficiency.
- the signaling efficiency of the PAFPs was measured in mammalian cells by transient transfection of A549 cells with the zyxin::PAFP constructs.
- conventional fluorescent microscopy was used and cells were imaged till the PAFPs were fully bleached.
- the number of imaged molecules in each cell was estimated by dividing the total photon count from the cell by the product of the average photon number per switching event (Table 1) and the average number of blinking events for each PAFP (Table 4).
- Table 4 The results indicate that mMaple again offers much higher signaling efficiency (7-70 folder higher) than the other red PAFPs, even in mammalian cells.
- PSCFP2 offers a comparable signaling efficiency to that of mMaple (Table 4).
- New PAFPs with high signaling efficiency and low dimerization tendency show that mMaple has a much higher signaling efficiency than all of the other tested PAFPs.
- the dimerization tendency of mMaple could lead to aggregation effects on the target proteins.
- Dendra2, mEos3.2, and PAtagRFP exhibit undetectable dimerization tendency, but have low signaling efficiency. It is thus desirable to develop a new PAFP that has both high signaling efficiency and low dimerization tendency.
- two new PAFPs were engineered by introducing point mutations into mMaple designed to destabilize the dimerization of this protein.
- mMaple2 Two mutations make mEos3.2 more monomeric than mEos2: 1102N and Y189A. Based on a sequence alignment between mEos2 and mMaple, comparable mutations were made, II 1 IN and Y198A, in mMaple. The properties of this new protein were tested. The protein was termed mMaple2. The properties were tested by fusing it to Zyxin, ClpP, and HupA and performing measurements on the photon budget, on-off ratio, dimerization tendency and signaling efficiency as described above. mMaple2 exhibited a similar photon budget, on-off ratio and signaling efficiency as those of mMaple (Fig. 5A, B, C, Table 1, 3, 4). ClpP-mMaple2 proteins still formed puncta in some cells. However, the percentage of cells with puncta was significantly reduced in comparison to ClpP-mMaple, suggesting a lower dimerization tendency of mMaple2 (Fig. 5D).
- FIG. 5A-5D Photon budget (Fig. 5A), on-off switching rate ratio (Fig. 5B), signaling efficiency (Fig. 5C) and dimerization tendency (Fig. 5D) of mMaple2 and mMaple3 in comparison with mMaple.
- FIG. 5D Sample fluorescent images of ClpP-mMaple2 and ClpP-mMaple3 expressing E. coli. Error bars are standard errors of the means and are too small to be visualized in (Fig. 5A).
- FIG. 5E H-NS appears more spread out in E.
- coli cells when fused to mMaple3 in comparison to the mMaple and mMaple2 fusion proteins.
- Tar-mMaple2 and Tar-mMaple3 appear more distributed along the cell envelope and less concentrated at the polar caps than Tar-mMaple.
- Fig. 5G Vimentin-mMaple2 and Vimentin-mMaple3 are less bundled than Vimentin-mMaple. (Scale bars: 1000 nm.)
- H-NS-mMaple3 Aggregation effects of mMaple2 and mMaple3 were tested on H-NS, Tar and Vimentin.
- H-NS-mMaple3 showed substantially more spread out H-NS distributions than H-NS-mMaple, though H-NS-mMaple2 still appeared as a few discrete clusters in each cell (Fig. 5E).
- Tar-mMaple2 and Tar-mMaple3 were substantially less concentrated at the cell poles than Tar-mMaple (Fig. 5F).
- Vimentin-mMaple2 and Vimentin-mMaple3 filaments were much less bundled than Vimentin-mMaple filaments (Fig. 5G). All of these observations are consistent with the reduced dimerization tendency of mMaple2 and the undetectable dimerization tendency of mMaple3.
- Figure 9 Excitation and emission spectra of mMaple, mMaple2 and mMaple3 before and after photo-conversion.
- the dashed lines are excitation spectra.
- the solid lines are emission spectra.
- the left lines are measurements before photo-conversion.
- the right lines are measurements after photo-conversion.
- the spectra are nearly identical among the three PAFPs.
- the photon budgets are not substantially different for different PAFPs within the same color group, but the red PAFPs provide substantially more photons (600- 900 photons per activation event) than the green PAFPs (200-300 photons). Even the red PAFPs' photon budgets are substantially lower than those of the bright
- photoswitchable/photoactivatable dyes (several thousand to one million photons) (7, 32). Given that the localization precision scales approximately linearly with the inverse square root of the photon numbers, the PAFPs thus give substantially lower localization precision than photo switchable dyes. Second, the on-off ratios are also not substantially different for different PAFPs within the same color group, but the red PAFPs tend to show much lower on-off ratio (10 ⁇ 5 - 10 "6 ) than the green PAFPs (-10 3 ). PSCFP2 is a noticeable exception with an on-off ratio similar to the red PAFPs.
- the on-off ratios of the red PAFPs are substantially lower than those of the popularly used photo swtichable dyes (10 ⁇ 3 - 10 "4 ), and hence PAFPs can provide substantially higher localization density.
- natural fluorescent proteins tend to dimerize or tetramerize. Although mutant fluorescent proteins have been made to reduce dimerization, many of the so-called monomeric fluorescent proteins still have some residual dimerization tendency and thus can cause undesired aggregation and mislocalization of the target proteins to which they are fused.
- the majority appeared to exhibit a substantial propensity towards aggregation or bundling of target proteins.
- the fourth property that was probed is the signaling efficiency, which determines the number of detectable molecules of the PAFP fusion protein for a given target protein.
- the signaling efficiency determines the number of detectable molecules of the PAFP fusion protein for a given target protein.
- the signaling efficiency is low, the number of localizations is not sufficient to map out the fine organization of the target protein.
- mMaple has the highest signaling efficiency, which is about one order of magnitude higher than the other PAFPs.
- the downside of mMaple is, however, its relatively high dimerization tendency.
- mMaple3 provides excellent performance in all four key properties described here, including high signaling efficiency, low dimerization tendency, high photon budget and low on-off ratio. In the cases that the localization number provided by mMaple3 is sub-optimal, one should also consider labeling with mMaple2, which will give substantially higher localization numbers, but it is important to check whether fusion with mMaple2 has led to undesired aggregation effect.
- the large number of localizations provided by mMaple2 and mMaple3 will not only facilitate mapping out the fine spatial distribution of the target protein, but will also allow the localizations to be divided into more snapshots to facilitate time-lapsed imaging of the dynamics of cellular structures.
- mEos3.2 and PAtagRFP are excellent choices for their high photon budget and undetectable dimerization tendency.
- the four properties measured in this work are four key properties of PAFPs to consider when imaging the spatial organization of a target protein with single-molecule- based super-resolution imaging. However, they are not the only important properties to consider when other experimental requirements need to be taken into account. For example, spectral properties are essential for multi-color imaging. For two-color imaging, green PAFPs are particularly useful (when paired with a red PAFP) even though they generally give lower photon numbers and higher on-off ratios. Dark-to- fluorescent PAFPs are also more favorable than color-changing PAFPs as the former take a smaller spectral space.
- the number of switching cycles is another important parameter to consider.
- PAFPs that can be switched on only once though almost all PAFPs tend to blink more than once.
- mapping of protein spatial organization a larger number of switching cycles per molecule would allow the target structure to be sampled multiple times, which can improve the image quality. This property is also advantageous when it comes to time-lapsed imaging for probing dynamics.
- RESOLFT reversibly switching fluorescent proteins with a large number of switching cycles (such as rsEGFP) may be required.
- New plasmids were constructed with PCR and isothermal assembly. E. coli chromosomal insertions were created by lambda RED recombination. E. coli cells were grown to exponential phase in M9 minimal media before imaging. Mammalian cell lines were transfected with purified plasmids using nucleofection or lipofection, and incubated for 24-26 hours before imaging. Phase-contrast, super-resolution or conventional fluorescence images were collected on an Olympus ⁇ -71 inverted microscope with 405- , 488-, and 561-nm laser lines. Images were analyzed with custom-written software. See below for details.
- E. coli codon- optimized PAFP sequences with a seven- amino-acid linker (SGGGGSK) (SEQ ID NO: 5) at the 5' ends were inserted into plasmid pBAD18, followed by a chloramphenicol resistance marker (cam). There are also two frt sites flanking the cam region.
- the cam markers in the clpP fusion constructs were later removed by Flp-frt recombination.
- the plasmids expressing Tar-PAFPs were designed with a pTrcHis2a (Life Technologies) backbone and direct fusion of PAFP sequences to the 3' end of tar.
- the plasmids for PAFP protein purification were cloned by inserting PAFP sequences into a pET-3a backbone (EMD Millipore), with an extra 10-amino-acid sequence after the start codon.
- the extra sequence codes for 6 histidines and a linker (CHHHHHHGSG) (SEQ ID NO: 6).
- the plasmid for HupA protein purification was cloned by inserting into pET-3a the hupA coding sequence, followed by a 3-amino-acid linker and 6 histidine codons at the 3' end (GSGHHHHHH) (SEQ ID NO: 7). All newly constructed plasmids and chromosomal insertions have been verified by sequencing.
- BS-C-1 cells grown at 37 °C in a 5% C02 atmosphere in Eagle Modified Minimum Essential Medium (ATCC) supplemented with 10% fetal bovine serum (Invitrogen) were transfected with pZyxin-PAFP plasmids using Amaxa cell line nucleofector kit V (Lonza) according to the manufacturer' s protocol, and plated in LabTek II 8-well chambered coverglass (Nunc). 24 hrs after transfection, live cells were washed with Dulbecco's Phosphate-buffered Saline (DPBS) and imaged.
- DPBS Dulbecco's Phosphate-buffered Saline
- E. coli strains expressing the ClpP-PAFP, H-NS-PAFP or HU-PAFP fusions were inoculated into lysogeny broth (LB), and grown to saturation overnight while shaking at 37 °C (unless otherwise stated).
- the LB cultures were then diluted 2000 times into M9 minimal media supplemented with 0.4% glucose, MEM amino acids and vitamins (Invitrogen), and further grown at 37 °C for ⁇ 5 hrs to an OD600nm of 0.15 (unless otherwise stated). 1 mL of each culture was concentrated 40 times by
- Cos7 cells grown at 37 °C in a 5% C0 2 atmosphere in Dulbecco's Modified Eagle Medium (Gibco) supplemented with 10% fetal bovine serum and MEM non-essential amino acids (Gibco) were transfected with the pVimentin-PAFP plasmids using Lipofectamine 2000 (Life Technologies) according to the manufacturer's protocol.
- PHEM buffer 25 mM HEPES, 10 mM EGTA, 60 mM PIPES, 2 mM MgC12, pH 6.9 for 15 minutes, rinsed three times in PHEM buffer, and imaged in DPBS.
- A549 cells grown in the same condition as Cos7 were transfected with pZyxin-PAFP plasmids using Lipofectamine 2000 according to the manufacturer's protocol.
- A549 cells were used for their higher transfection efficiency as compared to BS-C-1. 26 hrs after transfection, cells were fixed with 2% paraformaldehyde in PHEM buffer for 15 minutes. Cells were then rinsed three times in PHEM buffer, and imaged in DPBS.
- Optical setup and imaging conditions An Olympus IX-71 inverted microscope was used with a lOOx UPlanSApo, NA 1.40, oil immersion phase objective, and an active sample stabilization system.
- a 405 nm laser (CUBE 405-50C, Coherent) was used for photo-activation.
- a 488 nm laser (Sapphire 488-200CW, Coherent) was used to excite and image the green PAFPs.
- a 561 nm laser (Sapphire 561-200CW) was used to excite and image the red PAFPs.
- the power densities at the sample, with epi- fluorescence illumination were 0-1 kW/cm 2" at 405 nm, 390 W/cm 2" at 488 nm, and 1.8 kW/cm” at 561 nm.
- the illumination was further adjusted to near-TIRF (for bacteria) or TIR (for mammalian cells) configurations, which increased the power density by another factor of 3-4.
- a Di01-R561 (Semrock) dichroic mirror and an FF01-617/73 (Semrock) band pass emitter for the red PAFPs was used, or a
- ZT488RDC Chroma dichroic mirror and an ET525/50m (Chroma) band pass emitter for the green PAFPs.
- Movies of fluorescence images were acquired at 60 Hz. In most cases, super-resolution imaging was done with simultaneous illumination of the activation and excitation light, with gradual increase in the activation light power. For the on-off ratio measurements, super-resolution imaging of the Zyxin-PAFP samples was performed first without activation for 30 sec, and then gradually increased the activation power till the samples were fully imaged. For conventional fluorescence imaging, samples were simultaneously illuminated with the activation and excitation light.
- Image analysis The image processing procedure of the super-resolution images used known techniques. Conventional fluorescence images of ClpP-PAFP were obtained by averaging 120 frames of the 60-Hz movie. Other analyses, including cell segregation, punctum detection, statistical calculation, and curve fitting, were performed with MATLAB R2012a.
- This culture was diluted 1 in 200 into fresh medium and grown for 2 hours at 32 °C.
- Cells were harvested at an OD600 of 0.2-0.3.
- a single channel of a fluidics chamber (Ibidi ⁇ -Slide VI 0.4; 80606) was coated with 1% polyethylenimine (PEI, Aldrich) for 15 minutes at room temperature then washed twice with fresh medium. Freshly harvested cells were added to the channel, and the chamber was spun at 200G for 30 s to press the cells flat against the surface. The chamber was then washed five times with MOPS minimal defined medium (Teknova M2106) supplemented with 0.2% w/v glucose. This medium was also supplemented with 500 microgram/mL kanamycin to completely inhibit protein synthesis.
- MOPS minimal defined medium Teknova M2106
- Cells were harvested with centrifugation, and resuspended in 15 mL of native wash buffer (50 mM Tris, pH 8.0 / 200 mM NaCl / 5 mM Imidazole / 10 mM ⁇ / 0.5 mM benzamidine) with half of a tablet of protease inhibitor (Roche). Cells were lysed by sonication and the debris was spun down by centrifugation. 4mL of Ni-NTA agarose (Qiagen) were washed in sterile water by centrifugation, applied to the supernatant of cell lysate, and incubated at 4 °C for >1 hr.
- native wash buffer 50 mM Tris, pH 8.0 / 200 mM NaCl / 5 mM Imidazole / 10 mM ⁇ / 0.5 mM benzamidine
- Ni-NTA particles were then washed with 15 mL of native wash buffer by centrifugation, and transferred into a chromatography column (Bio-Rad, Poly-Prep).
- the particle matrix was washed with an additional 40 mL of native wash buffer by gravity flow, washed 1 final time with 1 mL of elution buffer (100 mM NaCl / 300 mM Imidazole pH 7.0 / 10 mM beta-ME), and then eluted in 1 mL fractions with elution buffer.
- the fractions containing PAFP were combined and dialyzed overnight in dialysis buffer (20 mM Tris, pH 7.5 / 100 mM NaCl / 1 mM EDTA / 10 mM beta-ME).
- dialysis buffer (20 mM Tris, pH 7.5 / 100 mM NaCl / 1 mM EDTA / 10 mM beta-ME).
- the excitation and emission spectra of the purified proteins were measured with a Cary Eclipse fluorescence spectrophotometer. Photo-conversion of the purified proteins was achieved by shining the 405-nm imaging laser on the protein solution.
- biotinylated PAFP molecules were sparsely immobilized on a streptavidin coated coverslip in a flow chamber.
- Purified PAFPs were biotinylated with ImmunoProbe Biotinylation Kit (Sigma- Aldrich) according to the manufacturer's protocol.
- Flow chambers and streptavidin coated coverslips were prepared.
- the biotinylated proteins were diluted in phosphate buffered saline (PBS) before being added into the chamber. After 1 min, the chamber was washed with PBS to remove unbound molecules.
- PBS phosphate buffered saline
- Immobilized PAFPs were imaged with the same microscope and settings as in previous super-resolution imaging. The density of immobilized molecules was kept low such that individual molecules were well resolved from each other. The numbers of blinking events were extracted with custom written programs.
- HupA protein solution used as concentration standard were prepared by transforming BL21(DE3)pLysS competent cells (Invitrogen) with the pET3a-hupA-6xHis plasmid. Protein purification procedure was the same as that described in the PAFP purification section. The size and purity of the protein were verified by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and SYPRO Red staining (Invitrogen). The concentration was determined with a bovine serum albumin standard.
- E. coli cells with hupA: :PAFP fusions were grown under the same condition as in the imaging experiments.
- the cell concentrations were estimated by optical density measurements and LB agar plating. 1 mL of cells were resuspended in 97 microliters of T200 buffer (50 mM Tris, pH 8 / 200 mM NaCl) plus 1 microliters of TURBO DNase (Life Technologies) and 2 microliters of Ready-Lyse Lysozyme (Epicentre). Cells were lysed by three freeze-thaw cycles in liquid nitrogen and 37 °C water bath.
- the HupA concentration standard or the lysed cell content solutions were mixed with 2x Laemmli Sample Buffer (BioRad) with a 1: 1 ratio, heat- denatured, separated by a 4-15% Tris-HCl Ready Gel PAGE gel (BioRad), and transferred to a Hybond-P membrane (GE Healthcare).
- the membrane was blocked with 5% milk (Nestle) in DPBS plus 0.1% Tween 20 (PBST) for 1 hr at room temperature.
- polycolonal anti-HU primary antibody (provided by Professor Jon Kaguni) was diluted 1:30,000 into the 5% milk in PBST and added to the membrane. After overnight incubation at 4 °C, the membrane was washed three times in PBST (7 min each).
- ECL HRP-linked donkey- anti-rabbit IgG (GE Healthcare) was diluted 1: 10,000 into 5% milk in PBST, added to the membrane, and incubated for 45 min at room temperature. After three more washes in PBST (7 min each),
- chemiluminescence signal was generated by Lumigen TMA-6 Reagent, and detected with an Alphalnnotech Chemilmager.
- Immunofluorescence sample preparation For the immunofluorescence imaging of Vimentin, untransfected Cos7 cells were fixed as in the PAFP imaging experiments. Then cells were blocked with a blocking buffer (DPBS with 3% BSA, 0.5% Triton-X- 100) for 15 min, and treated with ⁇ 1 microgram/mL mouse anti- Vimentin primary antibody (Invitrogen) in the blocking buffer for 30 min at room temperature.
- DPBS with 3% BSA, 0.5% Triton-X- 100 for 15 min, and treated with ⁇ 1 microgram/mL mouse anti- Vimentin primary antibody (Invitrogen) in the blocking buffer for 30 min at room temperature.
- the cells were washed three times (10 min each) with a wash buffer (DPBS with 0.2% BSA and 0.1% Triton-X-100), and then treated with -2.5 microgram /mL donkey anti-mouse secondary antibody conjugated with Alexa 647 (Jackson Immunoresearch) in the blocking buffer for 30 min at room temperature. Afterwards, cells were washed three times (10 min each) with the wash buffer and one more time with DPBS, and post-fixed with 3% paraformaldehyde and 0.1% glutaraldehyde for 10 min at room temperature. After three more washes with DPBS, the cells were imaged in the imaging buffer (DPBS with 1% ⁇ , 0.8% glucose, 1 mg/mL glucose oxidase and 40 microgram /mL catalase).
- DPBS 1% ⁇ , 0.8% glucose, 1 mg/mL glucose oxidase and 40 microgram /mL catalase
- km is inversely proportional to the PAFP maturation half-life ( m).
- kd is inversely proportional to the doubling time (rd) of E. coli under these growth condition.
- the maturation half-life of mMaple at 32 °C was measured to be 48 min and the doubling time of E. coli at 32 °C in the M9 media was determined to be 74 min. So the mature fraction for mMaple is 0.61.
- the expected ratio of mature fluorophores between two different PAFPs can be written as:
- the maturation half-life of mEos2 and mMaple at 32 °C are 340 and 48 min respectively.
- the expression levels of the two are similar (Table 3).
- the expected ratio of the cellular concentrations of the mature fluorophores should be a spk - 0.29
- the mature fraction is expected to be close to 1 due to the very long doubling time of the cells (-22 hrs for A549).
- the signaling efficiency of the slowly maturing PAFPs e.g. mEos2
- the signaling efficiency of the fast-maturing mMaple should improve in the mammalian cells.
- the improvement may not be large. If it is assumed the maturation half-lives of the PAFPs in mammalian cells are similar to those measured in E. coli, the expected improvement of the signaling efficiency of mEos2 relative to that of mMaple should only be ⁇ 2.8-fold.
- the phrase "at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements.
- This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase "at least one" refers, whether related or unrelated to those elements specifically identified.
- At least one of A and B can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.
Abstract
La présente invention concerne d'une manière générale des protéines fluorescentes, destinées à diverses utilisations telles que la microscopie à super résolution. Selon un ensemble de modes de réalisation, la protéine est mMAPLE2 ou mMAPLE3. Selon un autre ensemble de modes de réalisation, la protéine comprend deux substitutions ou plus dans mMAPLE. En outre, selon certains modes de réalisation, la présente invention concerne d'une manière générale des systèmes et des procédés de production ou d'utilisation de telles protéines, des kits comprenant de telles protéines, des acides nucléiques codant pour de telles protéines, des vecteurs ou des plasmides comprenant de telles protéines ou acides nucléiques, ou des cellules ou des organismes comprenant de telles protéines ou acides nucléiques, ainsi que des fragments, des homologues, des analogues, des dérivés ou des compositions fonctionnellement équivalentes.
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WO2021102122A1 (fr) | 2019-11-20 | 2021-05-27 | President And Fellows Of Harvard College | Procédés d'imagerie multifocale pour un profilage moléculaire |
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EP3270159A4 (fr) * | 2015-03-11 | 2018-08-08 | Kyoto University | Procédé d'observation utilisant une sonde de dissociation de liaison |
US10858688B2 (en) | 2015-03-11 | 2020-12-08 | Kyoto University | Observation method using binding and dissociation probe |
DE102017211031A1 (de) * | 2016-11-21 | 2018-05-24 | Carl Zeiss Microscopy Gmbh | Verfahren und Mikroskop zum Ermitteln einer Fluoreszenzintensität |
CN110114709A (zh) * | 2016-11-21 | 2019-08-09 | 卡尔蔡司显微镜有限责任公司 | 确定荧光强度的方法和显微镜 |
US11231576B2 (en) | 2016-11-21 | 2022-01-25 | Carl Zeiss Microscopy Gmbh | Method and microscope for determining a fluorescence intensity |
US11788123B2 (en) | 2017-05-26 | 2023-10-17 | President And Fellows Of Harvard College | Systems and methods for high-throughput image-based screening |
CN109285119A (zh) * | 2018-10-23 | 2019-01-29 | 百度在线网络技术(北京)有限公司 | 超分辨图像生成方法及装置 |
WO2021102122A1 (fr) | 2019-11-20 | 2021-05-27 | President And Fellows Of Harvard College | Procédés d'imagerie multifocale pour un profilage moléculaire |
EP4104860A4 (fr) * | 2020-02-10 | 2024-03-06 | Exostemtech Co Ltd | Exosome comprenant une protéine photoclivable, et utilisation associée |
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