Literature DB >> 12038765

Partial reduction and two-step modification of proteins for identification of disulfide bonds.

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:  

Mesh:

Substances:

Year:  2002        PMID: 12038765     DOI: 10.1021/ac015719j

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

1.  Experimental Assignment of Disulfide-Bonds in Purified Proteins.

Authors:  Hsin-Yao Tang; David W Speicher
Journal:  Curr Protoc Protein Sci       Date:  2019-02-12

2.  A new method for analysis of disulfide-containing proteins by matrix-assisted laser desorption ionization (MALDI) mass spectrometry.

Authors:  Hongmei Yang; Ning Liu; Xiaoyan Qiu; Shuying Liu
Journal:  J Am Soc Mass Spectrom       Date:  2009-09-03       Impact factor: 3.109

3.  Identification of the cysteine nitrosylation sites in human endothelial nitric oxide synthase.

Authors:  Monorama Tummala; Victor Ryzhov; Kandasamy Ravi; Stephen M Black
Journal:  DNA Cell Biol       Date:  2008-01       Impact factor: 3.311

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.