Literature DB >> 15649066

High-throughput method for N-terminal sequencing of proteins by MALDI mass spectrometry.

Minoru Yamaguchi1, Takashi Nakazawa, Hiroki Kuyama, Takashi Obama, Eiji Ando, Taka-aki Okamura, Norikazu Ueyama, Shigemi Norioka.   

Abstract

A high-throughput method for sequencing of N termini of proteins by using postsource decay (PSD) of matrix-assisted laser desorption/ionization mass spectrometry has been developed. After a protein blotted on the PVDF membrane was successively reduced, S-alkylated, and guanidinated, its N-amino group was coupled to biotinylcysteic acid. The protein was then extracted from the membrane and digested with trypsin. The derivatized N-terminal fragment was then specifically isolated from the tryptic digest with avidin resins, and its de novo sequencing was successfully performed by PSD utilizing a sulfonic acid group introduced to the N terminus.

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Year:  2005        PMID: 15649066     DOI: 10.1021/ac048776w

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


  2 in total

1.  Chemoenzymatic labeling of protein C-termini for positive selection of C-terminal peptides.

Authors:  Guoqiang Xu; Sung Bin Y Shin; Samie R Jaffrey
Journal:  ACS Chem Biol       Date:  2011-08-10       Impact factor: 5.100

2.  Solid-phase N-terminal peptide enrichment study by optimizing trypsin proteolysis on homoarginine-modified proteins by mass spectrometry.

Authors:  Saiful M Chowdhury; Gerhard R Munske; Jonathon Yang; Daria Zhukova; Hamilton Nguyen; James E Bruce
Journal:  Rapid Commun Mass Spectrom       Date:  2014-03-30       Impact factor: 2.419

  2 in total

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