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

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-term...

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Detalles Bibliográficos
Autores principales: Liu, Jiamei, Wei, Tongyao, Tan, Yi, Liu, Heng, Li, Xuechen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809390/
https://www.ncbi.nlm.nih.gov/pubmed/35222920
http://dx.doi.org/10.1039/d1sc06387a
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author Liu, Jiamei
Wei, Tongyao
Tan, Yi
Liu, Heng
Li, Xuechen
author_facet Liu, Jiamei
Wei, Tongyao
Tan, Yi
Liu, Heng
Li, Xuechen
author_sort Liu, Jiamei
collection PubMed
description 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.
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spelling pubmed-88093902022-02-24 Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs) Liu, Jiamei Wei, Tongyao Tan, Yi Liu, Heng Li, Xuechen Chem Sci Chemistry 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. The Royal Society of Chemistry 2021-12-28 /pmc/articles/PMC8809390/ /pubmed/35222920 http://dx.doi.org/10.1039/d1sc06387a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Jiamei
Wei, Tongyao
Tan, Yi
Liu, Heng
Li, Xuechen
Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title_full Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title_fullStr Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title_full_unstemmed Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title_short Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
title_sort enabling chemical protein (semi)synthesis via reducible solubilizing tags (rsts)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809390/
https://www.ncbi.nlm.nih.gov/pubmed/35222920
http://dx.doi.org/10.1039/d1sc06387a
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