Issue 10, 2017

Sortase A-mediated on-resin peptide cleavage and in situ ligation: an efficient one-pot strategy for the synthesis of functional peptides and proteins

Abstract

Sortase A was firstly found to recognize a PEGA resin supported peptide donor containing a LPXTG motif and to ligate with a suitable acceptor containing oligo-glycine to afford conjugates in one-pot. This approach combining enzymatic on-resin cleavage, activation and in situ ligation, was employed to synthesize dual functional peptides, modify peptides with lipids, biotin and PEG, as well as protein N-terminal labeling in high efficiency.

Graphical abstract: Sortase A-mediated on-resin peptide cleavage and in situ ligation: an efficient one-pot strategy for the synthesis of functional peptides and proteins

Supplementary files

Article information

Article type
Research Article
Submitted
17 Jun 2017
Accepted
16 Jul 2017
First published
17 Jul 2017

Org. Chem. Front., 2017,4, 2058-2062

Sortase A-mediated on-resin peptide cleavage and in situ ligation: an efficient one-pot strategy for the synthesis of functional peptides and proteins

X. Cheng, T. Zhu, H. Hong, Z. Zhou and Z. Wu, Org. Chem. Front., 2017, 4, 2058 DOI: 10.1039/C7QO00481H

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