3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde
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Names | |
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IUPAC name 4-(2-Formylquinoline-3-carbonyl)benzoic acid | |
Other names CBQCA, ATTO-TAG CBQCA | |
Identifiers | |
3D model (JSmol) | |
PubChem CID | |
CompTox Dashboard (EPA) | |
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Properties | |
C18H11NO4 | |
Molar mass | 305.289 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde (CBQCA) is a fluorogenic amine labeling dye that is not fluorescent itself, but covalently reacts with primary amines to form fluorescent products.[1] It was first reported in 1991.[2]
CBQCA is largely used in the context of quantifying peptides or proteins. Either cyanide or thiols are required as a co-substrate in the fluorogenic reaction, although thiols also react with and mask the CBQCA aldehyde thereby preventing the fluorogenic reaction against the targeted primary amines.[1] Once bound to protein the excitation wavelength is 465 nm (blue) and the emission wavelength is ~550 nm (green).[3]
Reaction
[edit]CBQCA, which is non-fluorescent, reacts with primary amines in the presence of cyanide to form fluorescent products:
See also
[edit]References
[edit]- ^ a b You, Wendy W.; Haugland, Rosaria P.; Ryan, Diane K.; Haugland, Richard P. (1997). "3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde, a Reagent with Broad Dynamic Range for the Assay of Proteins and Lipoproteins in Solution". Analytical Biochemistry. 244 (2). Elsevier BV: 277–282. doi:10.1006/abio.1996.9920. ISSN 0003-2697. PMID 9025944.
- ^ Liu, Jinping.; Hsieh, You Zoung.; Wiesler, Donald.; Novotny, Milos. (1991-03-01). "Design of 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde as a reagent for ultrasensitive determination of primary amines by capillary electrophoresis using laser fluorescence detection". Analytical Chemistry. 63 (5). American Chemical Society (ACS): 408–412. doi:10.1021/ac00005a004. ISSN 0003-2700. PMID 2064006.
- ^ Fisher Scientific, Thermo. "CBQCA Protein Quantitation Kit - Product Information" (PDF). Retrieved 7 April 2023.