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Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization
Thiol catalysts are essential in native chemical ligation (NCL) to increase the reaction efficiency. In this paper, we report the use of thiocholine in chemical protein synthesis, including NCL-based peptide ligation and metal-free desulfurization. Evaluation of thiocholine peptide thioester in term...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10179797/ https://www.ncbi.nlm.nih.gov/pubmed/37175065 http://dx.doi.org/10.3390/molecules28093655 |
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author | Suzuki, Sae Nakajima, Yuya Kamo, Naoki Osakabe, Akihisa Okamoto, Akimitsu Hayashi, Gosuke Murakami, Hiroshi |
author_facet | Suzuki, Sae Nakajima, Yuya Kamo, Naoki Osakabe, Akihisa Okamoto, Akimitsu Hayashi, Gosuke Murakami, Hiroshi |
author_sort | Suzuki, Sae |
collection | PubMed |
description | Thiol catalysts are essential in native chemical ligation (NCL) to increase the reaction efficiency. In this paper, we report the use of thiocholine in chemical protein synthesis, including NCL-based peptide ligation and metal-free desulfurization. Evaluation of thiocholine peptide thioester in terms of NCL and hydrolysis kinetics revealed its practical utility, which was comparable to that of other alkyl thioesters. Importantly, thiocholine showed better reactivity as a thiol additive in desulfurization, which is often used in chemical protein synthesis to convert Cys residues to more abundant Ala residues. Finally, we achieved chemical synthesis of two differently methylated histone H3 proteins via one-pot NCL and desulfurization with thiocholine. |
format | Online Article Text |
id | pubmed-10179797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101797972023-05-13 Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization Suzuki, Sae Nakajima, Yuya Kamo, Naoki Osakabe, Akihisa Okamoto, Akimitsu Hayashi, Gosuke Murakami, Hiroshi Molecules Article Thiol catalysts are essential in native chemical ligation (NCL) to increase the reaction efficiency. In this paper, we report the use of thiocholine in chemical protein synthesis, including NCL-based peptide ligation and metal-free desulfurization. Evaluation of thiocholine peptide thioester in terms of NCL and hydrolysis kinetics revealed its practical utility, which was comparable to that of other alkyl thioesters. Importantly, thiocholine showed better reactivity as a thiol additive in desulfurization, which is often used in chemical protein synthesis to convert Cys residues to more abundant Ala residues. Finally, we achieved chemical synthesis of two differently methylated histone H3 proteins via one-pot NCL and desulfurization with thiocholine. MDPI 2023-04-22 /pmc/articles/PMC10179797/ /pubmed/37175065 http://dx.doi.org/10.3390/molecules28093655 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Suzuki, Sae Nakajima, Yuya Kamo, Naoki Osakabe, Akihisa Okamoto, Akimitsu Hayashi, Gosuke Murakami, Hiroshi Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title | Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title_full | Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title_fullStr | Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title_full_unstemmed | Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title_short | Thiocholine-Mediated One-Pot Peptide Ligation and Desulfurization |
title_sort | thiocholine-mediated one-pot peptide ligation and desulfurization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10179797/ https://www.ncbi.nlm.nih.gov/pubmed/37175065 http://dx.doi.org/10.3390/molecules28093655 |
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