Derivatization of bile acids with taurine for analysis by fast atom bombardment mass spectrometry with collision-induced fragmentation.

Autor: J Zhang, WJ Griffiths, T Bergman, J Sjövall
Jazyk: angličtina
Rok vydání: 1993
Předmět:
Zdroj: Journal of Lipid Research, Vol 34, Iss 11, Pp 1895-1900 (1993)
Druh dokumentu: article
ISSN: 0022-2275
DOI: 10.1016/S0022-2275(20)35107-5
Popis: When analyzed by fast atom bombardment mass spectrometry, taurine-conjugated bile acids give intense [M-H]-pseudomolecular ions that can be subjected to collision-induced fragmentation to give structural information. A method has been developed that permits rapid coupling of taurine to unconjugated, glycine-conjugated, sulfated, and glucuronidated bile acids. The reaction is performed for 2 h at room temperature in aqueous pyridine hydrochloride buffer, with or without dioxane, using 0.1 M 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide as the coupling agent and 0.2 M taurine. The yields are higher than 95%. In contrast to published coupling reactions, the method permits conjugation of bile acids with the labile 7 alpha-hydroxy-3-oxo-4-ene structure.
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