Coomassie brilliant blue

Coomassie Brilliant Blue R-250
Skeletal formula of Coomassie brilliant blue R-250
Space-filling model of the coomassie brilliant blue R-250 molecule
Names
Other names
C.I. 42660, C.I. Acid Blue 83
Brilliant indocyanine 6B, Brillantindocyanin 6B
Brilliant Cyanine 6B, Serva Blue R
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.025.509 Edit this at Wikidata
EC Number
  • 228-060-5
UNII
  • InChI=1S/C45H45N3O7S2.Na/c1-4-47(31-33-9-7-11-43(29-33)56(49,50)51)40-23-15-36(16-24-40)45(35-13-19-38(20-14-35)46-39-21-27-42(28-22-39)55-6-3)37-17-25-41(26-18-37)48(5-2)32-34-10-8-12-44(30-34)57(52,53)54;/h7-30H,4-6,31-32H2,1-3H3,(H2,49,50,51,52,53,54);/q;+1/p-1
    Key: NKLPQNGYXWVELD-UHFFFAOYSA-M
  • CCN(CC1=CC(=CC=C1)S(=O)(=O)O)C2=CC=C(C=C2)C(=C3C=CC(=[N+](CC)CC4=CC(=CC=C4)S(=O)(=O)[O-])C=C3)C5=CC=C(C=C5)NC6=CC=C(C=C6)OCC.[Na+]
Properties
C45H44N3NaO7S2 (Sodium salt)
Molar mass 825.97 g/mol
Insoluble in cold, slightly soluble in hot (bright red blue)
Solubility in ethanol Slightly soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Coomassie brilliant blue G-250
Solid Coomassie brilliant blue G
Brilliant blue G in isopropanol solution
Names
Other names
C.I. 42655, C.I. Acid Blue 90
Brilliant indocyanine G, Brillantindocyanin G
Xylene Brilliant Cyanine G, Serva Blue G
Identifiers
3D model (JSmol)
ECHA InfoCard 100.025.509 Edit this at Wikidata
KEGG
  • CCN(CC1=CC(=CC=C1)S(=O)(=O)O)C2=CC(=C(C=C2)/C(=C\3/C=CC(=[N+](CC)CC4=CC(=CC=C4)S(=O)(=O)O)C=C3C)/C5=CC=C(C=C5)NC6=CC=C(C=C6)OCC)C
Properties
C47H50N3NaO7S2 (Sodium salt)
Molar mass 856.03 g/mol
Slightly soluble in cold, soluble in hot (bright blue)
Solubility in ethanol Soluble
Pharmacology
Legal status
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Coomassie brilliant blue is the name of two similar triphenylmethane dyes that were developed for use in the textile industry but are now commonly used for staining proteins in analytical biochemistry. Coomassie brilliant blue G-250 differs from Coomassie brilliant blue R-250 by the addition of two methyl groups. The name "Coomassie" is a registered trademark of Imperial Chemical Industries.

Name and discovery

The name Coomassie was adopted at the end of the 19th century as a trade name by the Blackley-based dye manufacturer Levinstein Ltd, in marketing a range of acid wool dyes.[2] In 1896 during the Fourth Anglo–Ashanti War, British forces had occupied the town of Coomassie (modern-day Kumasi in Ghana). In 1918 Levinstein Ltd became part of British Dyestuffs, which in 1926 became part of Imperial Chemical Industries.[3] Although ICI still owns the Coomassie trademark, the company no longer manufactures the dyes.

The blue disulfonated triphenylmethane dyes were first produced in 1913 by Max Weiler, who was based in Elberfeld, Germany.[4] Various patents were subsequently taken out on the organic synthesis.[5][6][7]

Papers published in biochemistry journals frequently refer to these dyes simply as "Coomassie" without specifying which dye was used. In fact, the Colour Index lists over 40 dyes with "Coomassie" in their name. There are also other Coomassie "blue" dyes. For example, the Merck Index (10th edition) lists Coomassie Blue RL (Acid Blue 92, C.I. 13390), which has a completely different structure.

Dye colour

The suffix "R" in the name of Coomassie brilliant blue R-250 is an abbreviation for "red" as the blue colour of the dye has a slight reddish tint. For the "G" variant the blue colour has a more greenish tint. The "250" originally denoted the purity of the dye.

The colour of the two dyes depends on the acidity of the solution. The "G" form of the dye has been studied in detail.[8] At a pH of less than 0 the dye has a red colour with an absorption maximum at a wavelength of 465 nm. At a pH of around 1 the dye is green with an absorption maximum at 620 nm while above pH 2 the dye is bright blue with a maximum at 595 nm. At pH 7 the dye has an extinction coefficient of 43,000 M−1 cm−1.[8]

The different colours are a result of the different charged states of the dye molecule. In the red form, all three nitrogen atoms carry a positive charge. The two sulfonic acid groups have extremely low pKa and will normally be negatively charged, thus at a pH of around zero the dye will be a cation with an overall charge of +1. The green colour corresponds to a form of the dye with no net overall charge. In neutral media (pH 7), only the nitrogen atom of the diphenylamine moiety carries a positive charge and the blue dye molecule is an anion with an overall charge of −1. The pKa values for the losses of the two protons are 1.15 and 1.82, respectively. The final proton is lost under alkaline conditions and the dye becomes pink (pKa 12.4).[8]

The dye interacts electrostatically but noncovalently with the amino and carboxyl groups of proteins. The dye molecules bind to proteins, including those in wool (keratin), to form a protein–dye complex. The formation of the complex stabilises the negatively charged anionic form of the dye, producing the blue colour, even under acid conditions when most of the molecules in solution are in the cationic form.[8] This is the basis of the Bradford assay, which quantifies protein by Coomassie brilliant blue dye binding. The binding of the dye to a protein causes a shift in the absorbance maximum of the dye from 465 to 595 nm. The increase of absorption at 595 nm is monitored to determine protein concentration.[9]

The dye also forms a complex with the anionic detergent sodium dodecylsulfate (SDS).[10] The formation of this complex stabilizes the neutral, green form of the dye. This effect can interfere with the estimation of protein concentration using the Bradford assay. It is also likely that the anionic detergent competes with the dye for binding to the protein.

Applications in biochemistry

Coomassie brilliant blue R-250 was first used to visualise proteins in 1963 by Fazekas de St. Groth and colleagues. Protein samples were separated electrophoretically on a cellulose acetate sheet. The sheet was then soaked in sulfosalicylic acid to fix the protein bands and transferred to a solution of the dye.[11]

Two years later in 1965 Meyer and Lambert used Coomassie brilliant blue R-250 to stain protein samples after electrophoretic separation in a polyacrylamide gel. They soaked the gel in a dye solution containing methanol, acetic acid and water. As the dye stained the polyacrylamide gel as well as the protein, in order to visualise the protein bands they needed to destain the gel, which they did electrophoretically.[12] Subsequent publications reported that polyacrylamide gels could be successfully destained using an acetic acid solution.

The first report of the use of the G form of the dye to visualise protein bands in polyacrylamide gels came in 1967, where the dye was dissolved in an acetic acid solution containing methanol.[13] It was subsequently discovered that the protein bands could be stained without staining the polyacrylamide by using a colloid of the G form of the dye in a trichloroacetic acid solution containing no methanol. With this procedure it was no longer necessary to destain the gel.[14] Modern formulations typically use a colloid of the G form of dye in a solution containing phosphoric acid, ethanol (or methanol) and ammonium sulfate (or aluminium sulfate).[15][16][17][18]

The Bradford assay uses the spectral properties of Coomassie brilliant blue G-250 to estimate the amount of protein in a solution.[19] A protein sample is added to a solution of the dye in phosphoric acid and ethanol. Under the acid conditions the dye is normally a brownish colour but on binding to the protein the blue form of the dye is produced. The optical absorbance of the solution is measured at a wavelength of 595 nm. The dye is noted for its high level of sensitivity: 5 μg of protein[clarification needed] can be detected. However, among the disadvantages of the method is its variability of color development with different proteins: the absorbance change per unit mass of proteins varies with the type of the protein.[20]

On binding to a protein, the negatively charged Coomassie brilliant blue G-250 dye molecule will give an overall negative charge to the protein. This property can be used to separate proteins or protein complexes using polyacrylamide gel electrophoresis under non-denaturing conditions in a technique called blue native PAGE.[21][22] The mobility of the complex in the polyacrylamide gel will depend on both the size of the protein complex (i.e., the molecular weight) and the amount of dye bound to the protein.

Coomassie blue staining can also be used as a loading control staining method in western blot analysis.[23] It is applied as an anionic pre-antibody stain.

Medical uses

In 2009, brilliant blue G was used in scientific experiments to treat spinal injuries in laboratory rats.[24] It acts by reducing the body's natural swelling response, which can cause neurons in the area to die of metabolic stress. Testing on the rats proved effective. In comparison to the rats that had not received the dye, the rats that were treated with the dye performed better on motion tests.[25] It is unknown whether this treatment can be used effectively in humans. The animal experiments administered the dye within 15 minutes of injury, but to be effective in a real-life setting, where it may take time for a patient to reach the emergency room, the treatment needs to be effective even when administered up to two hours after injury. The only reported side effect was that the rats temporarily turned blue.[24][26][27]

Under the trade names ILM Blue and Brilliant Peel, brilliant blue G is used as a stain to assist surgeons in retinal surgery.[28] In December 2019, brilliant blue G (under the trade name TissueBlue, DORC International, Netherlands) was approved for use in humans in the United States.[29][30][31]

Tissueblue was approved for medical use in Canada in January 2021.[32][33]

Application in forensic science

The ability of the Coomassie dye to target amino acids with aromatic groups (phenylalanine, tyrosine, tryptophan) and basic side chains (lysine, arginine and histidine) allows the Bradford assay to be used for fingerprint analysis. The assay was successfully used to identify the biological sex of the fingerprint. Female samples were shown to have a higher absorbance than male samples when tested at similar wavelengths. This provides a simpler method for fingerprint analysis by reducing the number of amino acids needing to be analyzed from 23 to 6 and requires little to no assay preparation, in contrast to the ninhydrin chemical assay, which requires assay preparation such as heating and enzyme cascade.[34]

References

  1. ^ "Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Retrieved 25 March 2024.
  2. ^ Fox, M. R. (1987). Dye-makers of Great Britain 1856-1976 : A History of Chemists, Companies, Products and Changes. Manchester: Imperial Chemical Industries. p. 38.
  3. ^ Fox, M. R. (1987). Dye-makers of Great Britain 1856-1976 : A History of Chemists, Companies, Products and Changes. Manchester: Imperial Chemical Industries. p. 259.
  4. ^ Colour Index (PDF). Vol. 4 (3rd ed.). Bradford: Society of Dyers and Colourists. 1971. pp. 4397–4398. Archived from the original (PDF) on 2011-07-19. Retrieved 2010-07-20.
  5. ^ FR patent 474260, "Procédé de production de colorants de la série du triarylméthane", issued 1915-02-16, assigned to Bayer 
  6. ^ US patent 1218232, Weiler, Max, "Blue Triphenylmethane Dye", issued 1917-03-06 
  7. ^ GB patent 275609, "Manufacture of Triarylmethane-dyestuffs", issued 1927-11-03, assigned to IG Farbenindustrie 
  8. ^ a b c d Chial, H. J.; Thompson, H. B.; Splittgerber, A. G. (1993). "A spectral study of the charge forms of Coomassie Blue G". Analytical Biochemistry. 209 (2): 258–266. doi:10.1006/abio.1993.1117. PMID 7682385.
  9. ^ Bradford, Marion M. (1976). "A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding" (PDF). Analytical Biochemistry. 72 (1–2): 248–254. doi:10.1016/0003-2697(76)90527-3. PMID 942051. S2CID 4359292.
  10. ^ Compton, S. J.; Jones, C. G. (1985). "Mechanism of dye response and interference in the Bradford protein assay". Analytical Biochemistry. 151 (2): 369–374. doi:10.1016/0003-2697(85)90190-3. PMID 4096375.
  11. ^ Fazekas de St. Groth, S.; Webster, R. G.; Datyner, A. (1963). "Two new staining procedures for quantitative estimation of proteins on electrophoretic strips". Biochimica et Biophysica Acta. 71: 377–391. doi:10.1016/0006-3002(63)91092-8. PMID 18421828.
  12. ^ Meyer, T. S.; Lambert, B. L. (1965). "Use of Coomassie brilliant blue R250 for the electrophoresis of microgram quantities of parotid saliva proteins on acrylamide-gel strips". Biochimica et Biophysica Acta (BBA) - General Subjects. 107 (1): 144–145. doi:10.1016/0304-4165(65)90403-4. PMID 4159310.
  13. ^ Altschul, A. M.; Evans, W. J. (1967). "Zone electrophoresis with polyacrylamide gel". Enzyme Structure. Methods in Enzymology. Vol. 11. pp. 179–186. doi:10.1016/S0076-6879(67)11019-7. ISBN 9780121818609.. Page 184 personal communication from W. J. Saphonov.
  14. ^ Diezel, W.; Kopperschläger, G.; Hofmann, E. (1972). "An improved procedure for protein staining in polyacrylamide gels with a new type of Coomassie Brilliant Blue". Analytical Biochemistry. 48 (2): 617–620. doi:10.1016/0003-2697(72)90117-0. PMID 4115985.
  15. ^ Neuhoff, V.; Stamm, R.; Eibl, H. (1985). "Clear background and highly sensitive protein staining with Coomassie Blue dyes in polyacrylamide gels: a systematic analysis". Electrophoresis. 6 (9): 427–448. doi:10.1002/elps.1150060905. S2CID 94797941.
  16. ^ Candiano, G.; Bruschi, M.; Musante, L.; Santucci, L.; Ghiggeri, G. M.; Carnemolla, B.; Orecchia, P.; Zardi, L.; Righetti, P. G. (2004). "Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis". Electrophoresis. 25 (9): 1327–1333. doi:10.1002/elps.200305844. PMID 15174055. S2CID 25960150.
  17. ^ Steinberg, T. H. (2009). "Chapter 31 Protein Gel Staining Methods". Guide to Protein Purification, 2nd Edition. Methods in Enzymology. Vol. 463. pp. 541–563. doi:10.1016/S0076-6879(09)63031-7. ISBN 9780123745361. PMID 19892191.
  18. ^ Pink, M.; Verma, N.; Rettenmeier, A. W.; Schmitz-Spanke, S. (2010). "CBB staining protocol with higher sensitivity and mass spectrometric compatibility". Electrophoresis. 31 (4): 593–598. doi:10.1002/elps.200900481. PMID 20162584. S2CID 39038371.
  19. ^ Bradford, M. M. (1976). "Rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding". Analytical Biochemistry. 72 (1–2): 248–254. doi:10.1016/0003-2697(76)90527-3. PMID 942051. S2CID 4359292.
  20. ^ Congdon, Robert W.; Muth, Gregory W.; Splittgerber, Allan G. (September 1993). "The binding interaction of Coomassie blue with proteins". Analytical Biochemistry. 213 (2): 407–413. doi:10.1006/abio.1993.1439. PMID 7694523.
  21. ^ Schägger, H.; Jagow, G. (1991). "Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form". Analytical Biochemistry. 199 (2): 223–231. doi:10.1016/0003-2697(91)90094-A. PMID 1812789.
  22. ^ Wittig, I.; Braun, H. P.; Schägger, H. (2006). "Blue native PAGE". Nature Protocols. 1 (1): 418–428. doi:10.1038/nprot.2006.62. PMID 17406264. S2CID 19715017.
  23. ^ Welinder, Charlotte; Ekblad, Lars (2011). "Coomassie Staining as Loading Control in Western Blot Analysis". Journal of Proteome Research. 10 (3): 1416–1419. doi:10.1021/pr1011476. PMID 21186791.
  24. ^ a b Peng, W.; Cotrina, M. L.; Han, X.; Yu, H.; Bekar, L.; Blum, L.; Takano, T.; Tian, G. F.; et al. (2009). "Systemic administration of an antagonist of the ATP-sensitive receptor P2X7 improves recovery after spinal cord injury". Proceedings of the National Academy of Sciences of the United States of America. 106 (30): 12489–12493. doi:10.1073/pnas.0902531106. PMC 2718350. PMID 19666625.
  25. ^ Ehrenberg, Rachel (23 September 2013). "Brilliant blue for the spine". Science News. Society for Science & the Public. Retrieved 9 December 2017.
  26. ^ "Blue M&Ms 'mend spinal injuries'". Telegraph. 2009-07-28. Retrieved 2010-01-19.
  27. ^ "Blue Food Dye Treats Spine Injury in Rats". Wired.com. 2009-07-27. Retrieved 2010-01-19.
  28. ^ Mennel, S.; Meyer, C. H.; Schmidt, J. C.; Kaempf, S.; Thumann, G. (2008). Trityl dyes patent blue V and brilliant blue G - clinical relevance and in vitro analysis of the function of the outer blood-retinal barrier. Developments in Ophthalmology. Vol. 42. pp. 101–114. doi:10.1159/000138988. ISBN 978-3-8055-8551-4. PMID 18535384.
  29. ^ "Drug Trials Snapshots: TissueBlue". U.S. Food and Drug Administration (FDA). 20 December 2019. Retrieved 17 March 2020.
  30. ^ "TissueBlue- brilliant blue g injection, solution". DailyMed. 29 December 2019. Retrieved 17 March 2020.
  31. ^ "Drug Approval Package: TissueBlue". U.S. Food and Drug Administration (FDA). 10 January 2020. Retrieved 17 March 2020.
  32. ^ "Summary Basis of Decision (SBD) for Tissueblue". Health Canada. 23 October 2014. Retrieved 29 May 2022.
  33. ^ "Health product highlights 2021: Annexes of products approved in 2021". Health Canada. 3 August 2022. Retrieved 25 March 2024.
  34. ^ Brunelle, Erica; Le, Anh Minh; Huynh, Crystal; Wingfield, Kelly; Halámková, Lenka; Agudelo, Juliana; Halámek, Jan (2017-04-04). "Coomassie Brilliant Blue G-250 Dye: An Application for Forensic Fingerprint Analysis". Analytical Chemistry. 89 (7): 4314–4319. doi:10.1021/acs.analchem.7b00510. ISSN 0003-2700. PMID 28293949.

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A Malayali girl sits with a Brahmin before the vidyarambham ceremony on Navaratri Hindu rite of passage for young children For the Malayalam film, see Vidhyarambham. Part of a series onHinduism Hindus History OriginsHistorical Hindu synthesis (500/200 BCE–300 CE) History Indus Valley Civilisation Historical Vedic religion Dravidian folk religion Śramaṇa Tribal religions in India Traditional Itihasa-Purana Epic-Puranic royal genealogies Epic-Puranic chronology Traditions Major traditions ...

 

Dutch footballer and manager Andries Jonker Jonker in 2010Personal informationFull name Andries Jonker[1]Date of birth (1962-09-22) 22 September 1962 (age 61)Place of birth Amsterdam, NetherlandsHeight 1.78 m (5 ft 10 in)Team informationCurrent team Netherlands (women)Youth career VolendamSenior career*Years Team Apps (Gls) De Volewijckers 0000–1980 Volendam 1980– De Volewijckers De Meer 0000–1988 ZFC Managerial career1988–1990 DRC Amsterdam II1999–2000 V...

Spirit in Basque mythology This article includes a list of references, related reading, or external links, but its sources remain unclear because it lacks inline citations. Please help improve this article by introducing more precise citations. (May 2015) (Learn how and when to remove this message) El aquelarre, Francisco Goya. Akerbeltz or Aker (from Basque aker, 'billy goat' and beltz, 'black') is a spirit in the folk mythology of the Basque people. It is said to live inside the land and is...

 

ナワ族Nahua総人口1,000,000(1979年)居住地域メキシコ言語ナワトル語宗教不明 ナワ族(ナワぞく、Nahua)は、メキシコに住む民族。原住民中最大の民族である。 ナワ族はメキシコ中央部のメキシコ盆地を中心とする地域に居住するが、伝説によれば、北方からやってきたと伝えられる。これは、ナワ族の言語であるナワトル語が北方系のユト・アステカ語族に属し、周辺�...