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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...

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Detalles Bibliográficos
Autores principales: Suzuki, Sae, Nakajima, Yuya, Kamo, Naoki, Osakabe, Akihisa, Okamoto, Akimitsu, Hayashi, Gosuke, Murakami, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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