Literature DB >> 18577371

A method for N-terminal de novo sequence analysis of proteins by matrix-assisted laser desorption/ionization mass spectrometry.

Hiroki Kuyama1, Kazuhiro Sonomura, Osamu Nishimura, Susumu Tsunasawa.   

Abstract

A novel method for isolation and de novo sequencing of N-terminal peptides from proteins is described. The method presented here combines selective chemical tagging using succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP-Ac-OSu) at the N(alpha)-amino group of peptides after digestion by metalloendopeptidase (from Grifola frondosa) and selective capture procedures using p-phenylenediisothiocyanate resin, by which the N-terminal peptide can be isolated, whether or not it is N-terminally blocked. The isolated N-terminal peptide modified N-terminally with TMPP-Ac-OSu reagent produces a simple fragmentation pattern under tandem mass spectrometric analysis to significantly facilitate sequencing.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18577371     DOI: 10.1016/j.ab.2008.05.053

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  2 in total

1.  Using chemical derivatization and mass spectrometric analysis to characterize the post-translationally modified Staphylococcus aureus surface protein G.

Authors:  Moo-Jin Suh; David J Clark; Prashanth P Parmer; Robert D Fleischmann; Scott N Peterson; Rembert Pieper
Journal:  Biochim Biophys Acta       Date:  2010-02-20

2.  Peptide Sequencing Directly on Solid Surfaces Using MALDI Mass Spectrometry.

Authors:  Zhan-Gong Zhao; Lalaine Anne Cordovez; Stephen Albert Johnston; Neal Woodbury
Journal:  Sci Rep       Date:  2017-12-19       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.