| Literature DB >> 29947435 |
Kang Jin1, Xuechen Li1.
Abstract
Cysteine-based native chemical ligation (NCL) has been a very powerful approach for convergent synthesis of peptides and proteins. However, owing to the low abundance of cysteine (Cys) in proteins, applications of NCL in protein chemical synthesis are limited. To expand the peptide ligation toolbox, NCL followed by desulfurization has been developed to enable peptide ligation at Xaa-Ala conjunctions, that is, formal "alanine ligation". In this regard, effective peptide desulfurization methods are critical. This Concept article summarizes the development of different desulfurization strategies for peptide and protein chemical synthesis.Entities:
Keywords: cysteine surrogates; desulfurization; native chemical ligation (NCL); one-pot synthesis; proteins
Mesh:
Substances:
Year: 2018 PMID: 29947435 DOI: 10.1002/chem.201802067
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236