Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Petri, László, Ábrányi-Balogh, Péter, Csorba, Noémi, Keeley, Aaron, Simon, József, Ranđelović, Ivan, Tóvári, József, Schlosser, Gitta, Szabó, Dániel, Drahos, László, Keserű, György M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
_version_ 1785024309787361280
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
work_keys_str_mv AT petrilaszlo activationfreesulfonylfluorideprobesforfragmentscreening
AT abranyibaloghpeter activationfreesulfonylfluorideprobesforfragmentscreening
AT csorbanoemi activationfreesulfonylfluorideprobesforfragmentscreening
AT keeleyaaron activationfreesulfonylfluorideprobesforfragmentscreening
AT simonjozsef activationfreesulfonylfluorideprobesforfragmentscreening
AT ranđelovicivan activationfreesulfonylfluorideprobesforfragmentscreening
AT tovarijozsef activationfreesulfonylfluorideprobesforfragmentscreening
AT schlossergitta activationfreesulfonylfluorideprobesforfragmentscreening
AT szabodaniel activationfreesulfonylfluorideprobesforfragmentscreening
AT drahoslaszlo activationfreesulfonylfluorideprobesforfragmentscreening
AT keserugyorgym activationfreesulfonylfluorideprobesforfragmentscreening