Literature DB >> 28526476

Revisiting ligation at selenomethionine: Insights into native chemical ligation at selenocysteine and homoselenocysteine.

Rebecca Notis Dardashti1, Norman Metanis2.   

Abstract

Selenomethionine (Sem) has been incorporated recombinantly into proteins many times to elucidate their structure and function. In this paper, we revisit incorporation via chemical protein synthesis to shed light on the mechanism of native chemical ligation. The effect of chalcogen position on ligation is investigated, and selenium-containing peptide ligation is optimized. Additionally, selective methylation is performed on selenolates in a peptide in the presence of unprotected thiols.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chemical protein synthesis; Native chemical ligation; Peptide methylation; Selenocysteine; Selenomethionine

Mesh:

Substances:

Year:  2017        PMID: 28526476     DOI: 10.1016/j.bmc.2017.05.006

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

1.  O-GlcNAcylation of High Mobility Group Box 1 (HMGB1) Alters Its DNA Binding and DNA Damage Processing Activities.

Authors:  Aaron T Balana; Anirban Mukherjee; Harsh Nagpal; Stuart P Moon; Beat Fierz; Karen M Vasquez; Matthew R Pratt
Journal:  J Am Chem Soc       Date:  2021-09-21       Impact factor: 16.383

Review 2.  Synthesis and semisynthesis of selenopeptides and selenoproteins.

Authors:  Jun Liu; Rujin Cheng; Sharon Rozovsky
Journal:  Curr Opin Chem Biol       Date:  2018-04-30       Impact factor: 8.822

3.  Selenolysine: A New Tool for Traceless Isopeptide Bond Formation.

Authors:  Rebecca Notis Dardashti; Shailesh Kumar; Shawn M Sternisha; Post Sai Reddy; Brian G Miller; Norman Metanis
Journal:  Chemistry       Date:  2020-03-31       Impact factor: 5.236

  3 in total

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