Literature DB >> 31880156

N, S-Double Labeling of N-Terminal Cysteines via an Alternative Conjugation Pathway with 2-Cyanobenzothiazole.

Wenjian Wang1, Jianmin Gao1.   

Abstract

Conjugation of 2-cyanobenzothiazole (CBT) with N-terminal cysteines (NCys) typically gives a luciferin product. We herein report an alternative reaction pathway leading to an N-terminal amidine rendering the side chain thiol available for further modification. Examination of peptide sequence dependence of this amidine conjugation reveals a tripeptide tag CIS that allows facile N, S-double labeling of a protein of interest with >90% yield. This alternative reaction pathway of CBT-NCys condensation presents a significant addition to the toolbox for site-specific protein modifications.

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Year:  2020        PMID: 31880156     DOI: 10.1021/acs.joc.9b02959

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Fast and Cysteine-Specific Modification of Peptides, Proteins and Bacteriophage Using Chlorooximes.

Authors:  Fa-Jie Chen; Mengmeng Zheng; Vincent Nobile; Jianmin Gao
Journal:  Chemistry       Date:  2022-03-10       Impact factor: 5.236

2.  N-Terminal cysteine mediated backbone-side chain cyclization for chemically enhanced phage display.

Authors:  Mengmeng Zheng; Fredrik Haeffner; Jianmin Gao
Journal:  Chem Sci       Date:  2022-06-30       Impact factor: 9.969

  2 in total

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