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Fluorophore

From Wikipedia, the free encyclopedia
(Redirected from Fluorescent dyes)
For uses and theory of fluorescence, see Fluorescence in the life sciences.
A fluorophore-labeled human cell.

A fluorophore (or fluorochrome, similarly to a chromophore) is a fluorescent chemical compound that can re-emit light upon light excitation. Fluorophores typically contain several combined aromatic groups, or planar or cyclic molecules with several π bonds.[1]

Fluorophores are sometimes used alone, as a tracer in fluids, as a dye for staining of certain structures, as a substrate of enzymes, or as a probe or indicator (when its fluorescence is affected by environmental aspects such as polarity or ions). More generally they are covalently bonded to macromolecules, serving as a markers (or dyes, or tags, or reporters) for affine or bioactive reagents (antibodies, peptides, nucleic acids). Fluorophores are notably used to stain tissues, cells, or materials in a variety of analytical methods, such as fluorescent imaging and spectroscopy.

Fluorescein, via its amine-reactive isothiocyanate derivative fluorescein isothiocyanate (FITC), has been one of the most popular fluorophores. From antibody labeling, the applications have spread to nucleic acids thanks to carboxyfluorescein. Other historically common fluorophores are derivatives of rhodamine (TRITC), coumarin, and cyanine.[2] Newer generations of fluorophores, many of which are proprietary, often perform better, being more photostable, brighter, or less pH-sensitive than traditional dyes with comparable excitation and emission.[3][4]

Fluorescence

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The fluorophore absorbs light energy of a specific wavelength and re-emits light at a longer wavelength. The absorbed wavelengths, energy transfer efficiency, and time before emission depend on both the fluorophore structure and its chemical environment, since the molecule in its excited state interacts with surrounding molecules. Wavelengths of maximum absorption (≈ excitation) and emission (for example, Absorption/Emission = 485 nm/517 nm) are the typical terms used to refer to a given fluorophore, but the whole spectrum may be important to consider. The excitation wavelength spectrum may be a very narrow or broader band, or it may be all beyond a cutoff level. The emission spectrum is usually sharper than the excitation spectrum, and it is of a longer wavelength and correspondingly lower energy. Excitation energies range from ultraviolet through the visible spectrum, and emission energies may continue from visible light into the near infrared region.

The main characteristics of fluorophores are:

  • Maximum excitation and emission wavelength (expressed in nanometers (nm)): corresponds to the peak in the excitation and emission spectra (usually one peak each).
  • Molar absorption coefficient (in mol−1cm−1): links the quantity of absorbed light, at a given wavelength, to the concentration of fluorophore in solution.
  • Quantum yield: efficiency of the energy transferred from incident light to emitted fluorescence (the number of emitted photons per absorbed photons).
  • Lifetime (in picoseconds): duration of the excited state of a fluorophore before returning to its ground state. It refers to the time taken for a population of excited fluorophores to decay to 1/e (≈0.368) of the original amount.
  • Stokes shift: the difference between the maximum excitation and maximum emission wavelengths.
  • Dark fraction: the proportion of the molecules not active in fluorescence emission. For quantum dots, prolonged single-molecule microscopy showed that 20-90% of all particles never emit fluorescence.[5] On the other hand, conjugated polymer nanoparticles (Pdots) show almost no dark fraction in their fluorescence.[6] Fluorescent proteins can have a dark fraction from protein misfolding or defective chromophore formation.[7]

These characteristics drive other properties, including photobleaching or photoresistance (loss of fluorescence upon continuous light excitation). Other parameters should be considered, as the polarity of the fluorophore molecule, the fluorophore size and shape (i.e. for polarization fluorescence pattern), and other factors can change the behavior of fluorophores.

Fluorophores can also be used to quench the fluorescence of other fluorescent dyes or to relay their fluorescence at even longer wavelengths.

Size (molecular weight)

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Most fluorophores are organic small molecules of 20–100 atoms (200–1000 Dalton; the molecular weight may be higher depending on grafted modifications and conjugated molecules), but there are also much larger natural fluorophores that are proteins: green fluorescent protein (GFP) is 27 kDa, and several phycobiliproteins (PE, APC...) are ≈240kDa. As of 2020, the smallest known fluorophore was claimed to be 3-hydroxyisonicotinaldehyde, a compound of 14 atoms and only 123 Da.[8]

Fluorescence particles like quantum dots (2–10 nm diameter, 100–100,000 atoms) are also considered fluorophores.[9]

The size of the fluorophore might sterically hinder the tagged molecule and affect the fluorescence polarity.

Families

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Fluorescence of different substances under UV light. Green is a fluorescein, red is Rhodamine B, yellow is Rhodamine 6G, blue is quinine, purple is a mixture of quinine and rhodamine 6g. Solutions are about 0.001% concentration in water.

Fluorophore molecules could be either utilized alone, or serve as a fluorescent motif of a functional system. Based on molecular complexity and synthetic methods, fluorophore molecules could be generally classified into four categories: proteins and peptides, small organic compounds, synthetic oligomers and polymers, and multi-component systems.[10][11]

Fluorescent proteins GFP, YFP, and RFP (green, yellow, and red, respectively) can be attached to other specific proteins to form a fusion protein, synthesized in cells after transfection of a suitable plasmid carrier.

Non-protein organic fluorophores belong to following major chemical families:

These fluorophores fluoresce due to delocalized electrons which can jump a band and stabilize the energy absorbed. For example, benzene, one of the simplest aromatic hydrocarbons, is excited at 254 nm and emits at 300 nm.[12] This discriminates fluorophores from quantum dots, which are fluorescent semiconductor nanoparticles.

They can be attached to proteins to specific functional groups, such as amino groups (active ester, carboxylate, isothiocyanate, hydrazine), carboxyl groups (carbodiimide), thiol (maleimide, acetyl bromide), and organic azide (via click chemistry or non-specifically (glutaraldehyde)).

Additionally, various functional groups can be present to alter their properties, such as solubility, or confer special properties, such as boronic acid which binds to sugars or multiple carboxyl groups to bind to certain cations. When the dye contains an electron-donating and an electron-accepting group at opposite ends of the aromatic system, this dye will probably be sensitive to the environment's polarity (solvatochromic), hence called environment-sensitive. Often dyes are used inside cells, which are impermeable to charged molecules; as a result of this, the carboxyl groups are converted into an ester, which is removed by esterases inside the cells, e.g., fura-2AM and fluorescein-diacetate.

The following dye families are trademark groups, and do not necessarily share structural similarities.

Bovine Pulmonary Artery Endothelial cell nuclei stained blue with DAPI, mitochondria stained red with MitoTracker Red CMXRos, and F-actin stained green with Alexa Fluor 488 phalloidin and imaged on a fluorescent microscope.

Examples of frequently encountered fluorophores

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Reactive and conjugated dyes

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Dye Ex (nm) Em (nm) MW Notes
Hydroxycoumarin 325 386 331 Succinimidyl ester
Aminocoumarin 350 445 330 Succinimidyl ester
Methoxycoumarin 360 410 317 Succinimidyl ester
Cascade Blue (375);401 423 596 Hydrazide
Pacific Blue 403 455 406 Maleimide
Pacific Orange 403 551
3-Hydroxyisonicotinaldehyde 385 525 123 QY 0.15; pH sensitive
Lucifer yellow 425 528
NBD 466 539 294 NBD-X
R-Phycoerythrin (PE) 480;565 578 240 k
PE-Cy5 conjugates 480;565;650 670 aka Cychrome, R670, Tri-Color, Quantum Red
PE-Cy7 conjugates 480;565;743 767
Red 613 480;565 613 PE-Texas Red
PerCP 490 675 35kDa Peridinin chlorophyll protein
TruRed 490,675 695 PerCP-Cy5.5 conjugate
FluorX 494 520 587 (GE Healthcare)
Fluorescein 495 519 389 FITC; pH sensitive
BODIPY-FL 503 512
G-Dye100 498 524 suitable for protein labeling and electrophoresis
G-Dye200 554 575 suitable for protein labeling and electrophoresis
G-Dye300 648 663 suitable for protein labeling and electrophoresis
G-Dye400 736 760 suitable for protein labeling and electrophoresis
Cy2 489 506 714 QY 0.12
Cy3 (512);550 570;(615) 767 QY 0.15
Cy3B 558 572;(620) 658 QY 0.67
Cy3.5 581 594;(640) 1102 QY 0.15
Cy5 (625);650 670 792 QY 0.28
Cy5.5 675 694 1272 QY 0.23
Cy7 743 767 818 QY 0.28
TRITC 547 572 444 TRITC
X-Rhodamine 570 576 548 XRITC
Lissamine Rhodamine B 570 590
Texas Red 589 615 625 Sulfonyl chloride
Allophycocyanin (APC) 650 660 104 k
APC-Cy7 conjugates 650;755 767 Far Red

Abbreviations:

Nucleic acid dyes

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Dye Ex (nm) Em (nm) MW Notes
Hoechst 33342 343 483 616 AT-selective
DAPI 345 455 AT-selective
Hoechst 33258 345 478 624 AT-selective
SYTOX Blue 431 480 ~400 DNA
Chromomycin A3 445 575 CG-selective
Mithramycin 445 575
YOYO-1 491 509 1271
Ethidium Bromide 210;285 605 394 in aqueous solution
GelRed 290;520 595 1239 Non-toxic substitute for Ethidium Bromide
Acridine Orange 503 530/640 DNA/RNA
SYTOX Green 504 523 ~600 DNA
TOTO-1, TO-PRO-1 509 533 Vital stain, TOTO: Cyanine Dimer
TO-PRO: Cyanine Monomer
Thiazole Orange 510 530
CyTRAK Orange 520 615 - (Biostatus) (red excitation dark)
Propidium Iodide (PI) 536 617 668.4
LDS 751 543;590 712;607 472 DNA (543ex/712em), RNA (590ex/607em)
7-AAD 546 647 7-aminoactinomycin D, CG-selective
SYTOX Orange 547 570 ~500 DNA
TOTO-3, TO-PRO-3 642 661
DRAQ5 600/647 697 413 (Biostatus) (usable excitation down to 488)
DRAQ7 599/644 694 ~700 (Biostatus) (usable excitation down to 488)

Cell function dyes

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Dye Ex (nm) Em (nm) MW Notes
Indo-1 361/330 490/405 1010 AM ester, low/high calcium (Ca2+)
Fluo-3 506 526 855 AM ester. pH > 6
Fluo-4 491/494 516 1097 AM ester. pH 7.2
DCFH 505 535 529 2'7'Dichorodihydrofluorescein, oxidized form
DHR 505 534 346 Dihydrorhodamine 123, oxidized form, light catalyzes oxidation
SNARF 548/579 587/635 pH 6/9

Fluorescent proteins

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Dye Ex (nm) Em (nm) MW QY BR PS Notes
GFP (Y66H mutation) 360 442
GFP (Y66F mutation) 360 508
EBFP 380 440 0.18 0.27 monomer
EBFP2 383 448 20 monomer
Azurite 383 447 15 monomer
GFPuv 385 508
T-Sapphire 399 511 0.60 26 25 weak dimer
Cerulean 433 475 0.62 27 36 weak dimer
mCFP 433 475 0.40 13 64 monomer
mTurquoise2 434 474 0.93 28 monomer
ECFP 434 477 0.15 3
CyPet 435 477 0.51 18 59 weak dimer
GFP (Y66W mutation) 436 485
mKeima-Red 440 620 0.24 3 monomer (MBL)
TagCFP 458 480 29 dimer (Evrogen)
AmCyan1 458 489 0.75 29 tetramer, (Clontech)
mTFP1 462 492 54 dimer
GFP (S65A mutation) 471 504
Midoriishi Cyan 472 495 0.9 25 dimer (MBL)
Wild Type GFP 396,475 508 26k 0.77
GFP (S65C mutation) 479 507
TurboGFP 482 502 26 k 0.53 37 dimer, (Evrogen)
TagGFP 482 505 34 monomer (Evrogen)
GFP (S65L mutation) 484 510
Emerald 487 509 0.68 39 0.69 weak dimer, (Invitrogen)
GFP (S65T mutation) 488 511
EGFP 488 507 26k 0.60 34 174 weak dimer, (Clontech)
Azami Green 492 505 0.74 41 monomer (MBL)
ZsGreen1 493 505 105k 0.91 40 tetramer, (Clontech)
TagYFP 508 524 47 monomer (Evrogen)
EYFP 514 527 26k 0.61 51 60 weak dimer, (Clontech)
Topaz 514 527 57 monomer
Venus 515 528 0.57 53 15 weak dimer
mCitrine 516 529 0.76 59 49 monomer
YPet 517 530 0.77 80 49 weak dimer
TurboYFP 525 538 26 k 0.53 55.7 dimer, (Evrogen)
ZsYellow1 529 539 0.65 13 tetramer, (Clontech)
Kusabira Orange 548 559 0.60 31 monomer (MBL)
mOrange 548 562 0.69 49 9 monomer
Allophycocyanin (APC) 652 657.5 105 kDa 0.68 heterodimer, crosslinked[13]
mKO 548 559 0.60 31 122 monomer
TurboRFP 553 574 26 k 0.67 62 dimer, (Evrogen)
tdTomato 554 581 0.69 95 98 tandem dimer
TagRFP 555 584 50 monomer (Evrogen)
DsRed monomer 556 586 ~28k 0.1 3.5 16 monomer, (Clontech)
DsRed2 ("RFP") 563 582 ~110k 0.55 24 (Clontech)
mStrawberry 574 596 0.29 26 15 monomer
TurboFP602 574 602 26 k 0.35 26 dimer, (Evrogen)
AsRed2 576 592 ~110k 0.21 13 tetramer, (Clontech)
mRFP1 584 607 ~30k 0.25 monomer, (Tsien lab)
J-Red 584 610 0.20 8.8 13 dimer
R-phycoerythrin (RPE) 565 >498 573 250 kDa 0.84 heterotrimer[13]
B-phycoerythrin (BPE) 545 572 240 kDa 0.98 heterotrimer[13]
mCherry 587 610 0.22 16 96 monomer
HcRed1 588 618 ~52k 0.03 0.6 dimer, (Clontech)
Katusha 588 635 23 dimer
P3 614 662 ~10,000 kDa phycobilisome complex[13]
Peridinin Chlorophyll (PerCP) 483 676 35 kDa trimer[13]
mKate (TagFP635) 588 635 15 monomer (Evrogen)
TurboFP635 588 635 26 k 0.34 22 dimer, (Evrogen)
mPlum 590 649 51.4 k 0.10 4.1 53
mRaspberry 598 625 0.15 13 monomer, faster photobleach than mPlum
mScarlet 569 594 0.70 71 277 monomer[14]

Advanced fluorescent proteins

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StayGold and mStayGold are advanced fluorescent proteins that have significantly contributed to the field of live-cell imaging. StayGold, known for its high photostability and brightness, was originally designed as a dimeric fluorescent protein, which, while effective, posed challenges related to the aggregation and labelling accuracy.[15] To address these limitations, mStayGold was engineered as a monomeric variant, enhancing its utility in precise protein labeling. mStayGold exhibits superior photostability, maintaining fluorescence under high irradiance conditions and demonstrates increased brightness compared to its former variant StayGold. Additionally, it matures faster, allowing for quicker imaging post-transfection. These advancements make mStayGold a versatile tool for a variety of applications, including single molecule tracking and high resolution imaging of dynamic cellular processes, thereby expanding the capabilities of fluorescent protein in biological research.[16]

Abbreviations:

Applications

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Further information: Fluorescence in the life sciences

Fluorophores have particular importance in the field of biochemistry and protein studies, for example, in immunofluorescence, cell analysis,[17] immunohistochemistry,[3][18] and small molecule sensors.[19][20]

Uses outside the life sciences

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Fluorescent sea dye

Fluorescent dyes find a wide use in industry, going under the name of "neon colors", such as:

See also

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References

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  1. ^ Juan Carlos Stockert, Alfonso Blázquez-Castro (2017). "Chapter 3 Dyes and Fluorochromes". Fluorescence Microscopy in Life Sciences. Bentham Science Publishers. pp. 61–95. ISBN 978-1-68108-519-7. Retrieved 24 December 2017.
  2. ^ Rietdorf J (2005). Microscopic Techniques. Advances in Biochemical Engineering / Biotechnology. Berlin: Springer. pp. 246–9. ISBN 3-540-23698-8. Retrieved 2008-12-13.
  3. ^ a b Tsien RY; Waggoner A (1995). "Fluorophores for confocal microscopy". In Pawley JB (ed.). Handbook of biological confocal microscopy. New York: Plenum Press. pp. 267–74. ISBN 0-306-44826-2. Retrieved 2008-12-13.
  4. ^ Lakowicz, JR (2006). Principles of fluorescence spectroscopy (3rd ed.). Springer. p. 954. ISBN 978-0-387-31278-1.
  5. ^ Pons T, Medintz IL, Farrell D, Wang X, Grimes AF, English DS, Berti L, Mattoussi H (2011). "Single-molecule colocalization studies shed light on the idea of fully emitting versus dark single quantum dots". Small. 7 (14): 2101–2108. doi:10.1002/smll.201100802. PMID 21710484.
  6. ^ Koner AL, Krndija D, Hou Q, Sherratt DJ, Howarth M (2013). "Hydroxy-terminated conjugated polymer nanoparticles have near-unity bright fraction and reveal cholesterol-dependence of IGF1R nanodomains". ACS Nano. 7 (2): 1137–1144. doi:10.1021/nn3042122. PMC 3584654. PMID 23330847.
  7. ^ Garcia-Parajo MF, Segers-Nolten GM, Veerman JA, Greve J, van Hulst NF (2000). "Real-time light-driven dynamics of the fluorescence emission in single green fluorescent protein molecules". PNAS. 97 (13): 7237–7242. Bibcode:2000PNAS...97.7237G. doi:10.1073/pnas.97.13.7237. PMC 16529. PMID 10860989.
  8. ^ Cozens, Tom (2020-12-16). "Fluorescent molecule breaks size record for green-emitting dyes". chemistryworld.com. Retrieved 2021-12-03.
  9. ^ Li Z, Zhao X, Huang C, Gong X (2019). "Recent advances in green fabrication of luminescent solar concentrators using nontoxic quantum dots as fluorophores". J. Mater. Chem. C. 7 (40): 12373–12387. doi:10.1039/C9TC03520F. S2CID 203003761.
  10. ^ Liu, J.; Liu, C.; He, W. (2013), "Fluorophores and Their Applications as Molecular Probes in Living Cells", Curr. Org. Chem., 17 (6): 564–579, doi:10.2174/1385272811317060003
  11. ^ Juan Carlos Stockert, Alfonso Blázquez-Castro (2017). "Chapter 4 Fluorescent Labels". Fluorescence Microscopy in Life Sciences. Bentham Science Publishers. pp. 96–134. ISBN 978-1-68108-519-7. Retrieved 24 December 2017.
  12. ^ Omlc.ogi.edu
  13. ^ a b c d e Columbia Biosciences
  14. ^ Bindels, Daphne S.; Haarbosch, Lindsay; van Weeren, Laura; Postma, Marten; Wiese, Katrin E.; Mastop, Marieke; Aumonier, Sylvain; Gotthard, Guillaume; Royant, Antoine; Hink, Mark A.; Gadella, Theodorus W. J. (January 2017). "mScarlet: a bright monomeric red fluorescent protein for cellular imaging". Nature Methods. 14 (1): 53–56. doi:10.1038/nmeth.4074. ISSN 1548-7105. PMID 27869816. S2CID 3539874.
  15. ^ Hirano, Masahiko; Ando, Ryoko; Shimozono, Satoshi; Sugiyama, Mayu; Takeda, Noriyo; Kurokawa, Hiroshi; Deguchi, Ryusaku; Endo, Kazuki; Haga, Kei; Takai-Todaka, Reiko; Inaura, Shunsuke; Matsumura, Yuta; Hama, Hiroshi; Okada, Yasushi; Fujiwara, Takahiro (July 2022). "A highly photostable and bright green fluorescent protein". Nature Biotechnology. 40 (7): 1132–1142. doi:10.1038/s41587-022-01278-2. ISSN 1546-1696. PMC 9287174. PMID 35468954.
  16. ^ Ando, Ryoko; Shimozono, Satoshi; Ago, Hideo; Takagi, Masatoshi; Sugiyama, Mayu; Kurokawa, Hiroshi; Hirano, Masahiko; Niino, Yusuke; Ueno, Go; Ishidate, Fumiyoshi; Fujiwara, Takahiro; Okada, Yasushi; Yamamoto, Masaki; Miyawaki, Atsushi (April 2024). "StayGold variants for molecular fusion and membrane-targeting applications". Nature Methods. 21 (4): 648–656. doi:10.1038/s41592-023-02085-6. ISSN 1548-7105. PMC 11009113. PMID 38036853.
  17. ^ Sirbu, Dumitru; Luli, Saimir; Leslie, Jack; Oakley, Fiona; Benniston, Andrew C. (2019). "Enhanced in vivo Optical Imaging of the Inflammatory Response to Acute Liver Injury in C57BL/6 Mice Using a Highly Bright Near-Infrared BODIPY Dye". ChemMedChem. 14 (10): 995–999. doi:10.1002/cmdc.201900181. ISSN 1860-7187. PMID 30920173. S2CID 85544665.
  18. ^ Taki, Masayasu (2013). "Chapter 5. Imaging and sensing of cadmium in cells". In Astrid Sigel; Helmut Sigel; Roland K. O. Sigel (eds.). Cadmium: From Toxicology to Essentiality. Metal Ions in Life Sciences. Vol. 11. Springer. pp. 99–115. doi:10.1007/978-94-007-5179-8_5. PMID 23430772.
  19. ^ Sirbu, Dumitru; Butcher, John B.; Waddell, Paul G.; Andras, Peter; Benniston, Andrew C. (2017-09-18). "Locally Excited State-Charge Transfer State Coupled Dyes as Optically Responsive Neuron Firing Probes" (PDF). Chemistry - A European Journal. 23 (58): 14639–14649. doi:10.1002/chem.201703366. ISSN 0947-6539. PMID 28833695.
  20. ^ Jiang, Xiqian; Wang, Lingfei; Carroll, Shaina L.; Chen, Jianwei; Wang, Meng C.; Wang, Jin (2018-08-20). "Challenges and Opportunities for Small-Molecule Fluorescent Probes in Redox Biology Applications". Antioxidants & Redox Signaling. 29 (6): 518–540. doi:10.1089/ars.2017.7491. ISSN 1523-0864. PMC 6056262. PMID 29320869.
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