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Activation-Free Sulfonyl Fluoride Probes for Fragment Screening
SuFEx chemistry is based on the unique reactivity of the sulfonyl fluoride group with a range of nucleophiles. Accordingly, sulfonyl fluorides label multiple nucleophilic amino acid residues, making these reagents popular in both chemical biology and medicinal chemistry applications. The reactivity...
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/PMC10096327/ https://www.ncbi.nlm.nih.gov/pubmed/37049805 http://dx.doi.org/10.3390/molecules28073042 |
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author | Petri, László Ábrányi-Balogh, Péter Csorba, Noémi Keeley, Aaron Simon, József Ranđelović, Ivan Tóvári, József Schlosser, Gitta Szabó, Dániel Drahos, László Keserű, György M. |
author_facet | Petri, László Ábrányi-Balogh, Péter Csorba, Noémi Keeley, Aaron Simon, József Ranđelović, Ivan Tóvári, József Schlosser, Gitta Szabó, Dániel Drahos, László Keserű, György M. |
author_sort | Petri, László |
collection | PubMed |
description | SuFEx chemistry is based on the unique reactivity of the sulfonyl fluoride group with a range of nucleophiles. Accordingly, sulfonyl fluorides label multiple nucleophilic amino acid residues, making these reagents popular in both chemical biology and medicinal chemistry applications. The reactivity of sulfonyl fluorides nominates this warhead chemotype as a candidate for an external, activation-free general labelling tag. Here, we report the synthesis and characterization of a small sulfonyl fluoride library that yielded the 3-carboxybenzenesulfonyl fluoride warhead for tagging tractable targets at nucleophilic residues. Based on these results, we propose that coupling diverse fragments to this warhead would result in a library of sulfonyl fluoride bits (SuFBits), available for screening against protein targets. SuFBits will label the target if it binds to the core fragment, which facilitates the identification of weak fragments by mass spectrometry. |
format | Online Article Text |
id | pubmed-10096327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100963272023-04-13 Activation-Free Sulfonyl Fluoride Probes for Fragment Screening Petri, László Ábrányi-Balogh, Péter Csorba, Noémi Keeley, Aaron Simon, József Ranđelović, Ivan Tóvári, József Schlosser, Gitta Szabó, Dániel Drahos, László Keserű, György M. Molecules Article SuFEx chemistry is based on the unique reactivity of the sulfonyl fluoride group with a range of nucleophiles. Accordingly, sulfonyl fluorides label multiple nucleophilic amino acid residues, making these reagents popular in both chemical biology and medicinal chemistry applications. The reactivity of sulfonyl fluorides nominates this warhead chemotype as a candidate for an external, activation-free general labelling tag. Here, we report the synthesis and characterization of a small sulfonyl fluoride library that yielded the 3-carboxybenzenesulfonyl fluoride warhead for tagging tractable targets at nucleophilic residues. Based on these results, we propose that coupling diverse fragments to this warhead would result in a library of sulfonyl fluoride bits (SuFBits), available for screening against protein targets. SuFBits will label the target if it binds to the core fragment, which facilitates the identification of weak fragments by mass spectrometry. MDPI 2023-03-29 /pmc/articles/PMC10096327/ /pubmed/37049805 http://dx.doi.org/10.3390/molecules28073042 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 Petri, László Ábrányi-Balogh, Péter Csorba, Noémi Keeley, Aaron Simon, József Ranđelović, Ivan Tóvári, József Schlosser, Gitta Szabó, Dániel Drahos, László Keserű, György M. Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title | Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title_full | Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title_fullStr | Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title_full_unstemmed | Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title_short | Activation-Free Sulfonyl Fluoride Probes for Fragment Screening |
title_sort | activation-free sulfonyl fluoride probes for fragment screening |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096327/ https://www.ncbi.nlm.nih.gov/pubmed/37049805 http://dx.doi.org/10.3390/molecules28073042 |
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