Premium
Bismuth(III) Complexes of the Tripeptide Glutathione (γ‐L‐Glu–L‐Cys–Gly)
Author(s) -
Sadler Peter J.,
Sun Hongzhe,
Li Hongyan
Publication year - 1996
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.19960020615
Subject(s) - tripeptide , chemistry , glutathione , titration , deprotonation , nuclear magnetic resonance spectroscopy , aqueous solution , stereochemistry , chelation , in vivo , thiol , inorganic chemistry , medicinal chemistry , nuclear chemistry , organic chemistry , peptide , biochemistry , enzyme , ion , microbiology and biotechnology , biology
Abstract The tripeptide glutathione (γ‐ L ‐Glu‐ L ‐Cys‐Gly, GSH) is thought to play an important role in the pharmacology of bismuth drugs, but to our knowledge no chemical studies of bismuth glutathione complexes have been reported. We report here studies of interactions of the antiulcer compound ranitidine bismuth citrate (1) and [Bi(edta)] − with glutathione in aqueous solution and in intact red blood cells by NMR spectroscopy. The deprotonated thiol group is shown to be the strongest binding site for Bi III , and a complex with the stoichiometry [Bi(GS) 3 ] is formed, as determined by 13 C NMR titrations. A remarkably large lowfield shift of approximately 1.37 ppm for the β‐CH 2 1 H NMR resonances of GSH was observed on binding to Bi III . The complex [Bi(GS) 3 ] is stable over the pH * range 2–10 (pH * = pH meter reading in D 2 O solution). A formation constant log K of 29.6±0.4 ( I = 0.1 M, 298 K) for [Bi(GS) 3 ] was determined by displacement of edta by GSH. The rate of exchange of GSH between free and bound forms is pH‐dependent, ranging from slow exchange (on the 1 H NMR timescale) at low pH (ca. 3 s −1 at pH 4.0) to intermediate exchange at biological pH (ca. 1500 s −1 ). Such facile exchange may be important in the transport and delivery of Bi III in vivo. Spin‐echo 1 H NMR showed that 1 reacts with GSH in red cells both in vivo and in vitro. A first‐order reaction of 1 with red blood cells was observed in vitro ( k = 0.20±0.04 h −1 , t 1/2 = 3 h, 310 K), and the rate‐determining step appeared to involve the passage of Bi III through the cell membrane.