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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8809390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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