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Interactions of alkyltin salts with biological dithiols: Dealkylation and induction of a regular beta-turn structure in peptides

Authors :
Buck, Bethany A.
Mascioni, Alessandro
Cramer, Christopher J.
Veglia, Gianluigi
Source :
Journal of the American Chemical Society. Nov 10, 2004, Vol. 126 Issue 44, 14400-14410
Publication Year :
2004

Abstract

The high-resolution NMR study and DFT calculation of the interaction between alkyltin compounds and a biological molecule are reported. It was seen that 9-residue peptide containing a CXC motif extracted from the neuronal peptide stannin (SNN) has no preferred structure, but upon the addition of trimethyltin (TMT), dealkylates TMT to dimethyltin (DMT), and adopts a unique stable type-I beta-turn conformation.

Details

Language :
English
ISSN :
00027863
Volume :
126
Issue :
44
Database :
Gale General OneFile
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
edsgcl.126137616