Issue 5, 2022

Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)

Abstract

Chemical synthesis of proteins with poor solubility presents a challenging task. The existing solubilizing tag strategies are not suitable for the expressed protein segment. To address this issue, we report herein that solubilizing tags could be introduced at the side chain of the peptide and C-terminal peptide salicylaldehyde esters via a disulfide linker. Such reducible solubilizing tags (RSTs) are compatible with peptide salicylaldehyde ester-mediated Ser/Thr ligation and Cys/Pen ligation for purifying and ligating peptides with poor solubility. This strategy features operational simplicity and readily accessible materials. Both the protein 2B4 cytoplasmic tail and FCER1G protein have been successfully synthesized via this strategy. Of particular note, the RST strategy could be used for solubilizing the expressed protein segment for protein semi-synthesis of the HMGB1 protein.

Graphical abstract: Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)

Supplementary files

Article information

Article type
Edge Article
Submitted
17 Nov 2021
Accepted
27 Dec 2021
First published
28 Dec 2021
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2022,13, 1367-1374

Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)

J. Liu, T. Wei, Y. Tan, H. Liu and X. Li, Chem. Sci., 2022, 13, 1367 DOI: 10.1039/D1SC06387A

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