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Understanding base‐assisted desulfurization using a variety of disulfide‐bridged peptides
Author(s) -
Galande Amit K.,
Trent John O.,
Spatola Arno F.
Publication year - 2003
Publication title -
peptide science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.10532
Subject(s) - chemistry , lanthionine , dehydroalanine , cysteine , cystine , peptide , heteronuclear single quantum coherence spectroscopy , stereochemistry , nuclear magnetic resonance spectroscopy , amino acid , combinatorial chemistry , organic chemistry , biochemistry , enzyme
A recently rediscovered reaction of base‐assisted lanthionine formation has been applied to several systems of disulfide‐bridged peptides. In addition to previously described nonapeptides consisting of i, i+3 cystine linkages, the reaction has now been extended to systems consisting of shorter (i, i+2) and longer (i, i+4) disulfide bridges. The desulfurization reaction is also compatible with disulfide bridges formed through homocysteines and penicillamines, yielding unusual amino acids such as cystathionine and β,β‐dimethyl lanthionine (referred to as “penthionine”) in a peptide chain, respectively. Systematic study of this transformation has provided several new insights into its mechanism. We have observed formation of dehydroalanine and dehydrovaline residues resulting from i, i+2‐bridged cysteines and i, i+3‐bridged cysteine/penicillamine peptides, respectively, thereby supporting a β‐elimination/Michael‐addition mechanism for this transformation. Amino acid analysis and NMR data from total correlation spectroscopy (TOCSY) and 1 H‐ 13 C heteronuclear single quantum correlation (HSQC) experiments show three diastereomeric lanthionine‐bridged peptides in the product mixture. But in the case of desulfurization of a cysteine/homocysteine containing disulfide‐bridged peptide, Michael addition appears to be stereoselective, yielding a single stereoisomer of cystathionine within the peptide. According to molecular modeling and CD spectroscopy, constrained peptides such as those containing penicillamine are less likely to undergo facile desulfurization. Flexibility of the torsional angles (C α H—C α —C β —S) corresponding to the cysteine residues and temperature appear to be contributing factors determining the extent of desulfurization. © 2003 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 71: 534–551, 2003