| Literature DB >> 12038765 |
Volker Schnaible1, Stephan Wefing, Anne Bücker, Sybille Wolf-Kümmeth, Daniel Hoffmann.
Abstract
An experimental protocol was established to combine partial reduction, cyanylation, and a second modification step for the assignment of disulfide bonds in proteins that are resistant to proteolysis under native conditions. After proteolysis, disulfide bonds were assigned via MALDI mass spectrometry with subsequent semiautomatic interpretation using the program SearchXLinks, which enumerates all possible combinations of proteolytic fragments for all observed monoisotopic masses. The putative assignment of disulfide bonds was confirmed by ISD and PSD fragmentation of the corresponding protonated molecules.Entities:
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Year: 2002 PMID: 12038765 DOI: 10.1021/ac015719j
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986