A twist in the tale: shifting from covalent targeting of a tyrosine in JAK3 to a lysine in MK2

While cysteine targeting in kinases is well established and widely used, covalent interactions with other amino acids remain much less explored. We aimed to develop covalent inhibitors targeting tyrosine residues in the protein kinases JAK3 and MK2 using structure-based design principles to generate small sets of ligands containing tyrosine-reactive sulfonyl fluoride and the less-explored fluorosulfate warheads. While the JAK3 inhibitors failed to achieve covalent binding, the fluorosulfate-bearing MK2 inhibitor 42, which had been designed as an allosteric binder, unexpectedly formed a bond with the "catalytic" lysine, additionally uncovering a unique interaction at the hinge region. This highlights the untapped potential of fluorosulfates and provides a rare example of the use of this electrophile for lysine targeting in kinases. Our results highlight the limitations of traditional design methods and support the integration of fragment/lead-like covalent library screening to discover unanticipated interactions.

Authors

Institutions

Publication Details

Journal
RSC Medicinal Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5md00440c
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A twist in the tale: shifting from covalent targeting of a tyrosine in JAK3 to a lysine in MK2

Michael Lämmerhofer, Stefan Knapp, Matthias Gehringer, Stefan Laufer et al.
RSC Medicinal Chemistry
Cytokine Signaling Pathways and Interactions
article

A twist in the tale: shifting from covalent targeting of a tyrosine in JAK3 to a lysine in MK2

Michael Lämmerhofer, Stefan Knapp, Matthias Gehringer, Stefan Laufer, Guiqun Wang, E. R. Gunther, Laura Hillebrand, Antti Poso, Benedikt Masberg, A. Chaikuad, Thales Kronenberger, Alexander Rasch, Michael Förster
article en

Abstract

While cysteine targeting in kinases is well established and widely used, covalent interactions with other amino acids remain much less explored. We aimed to develop covalent inhibitors targeting tyrosine residues in the protein kinases JAK3 and MK2 using structure-based design principles to generate small sets of ligands containing tyrosine-reactive sulfonyl fluoride and the less-explored fluorosulfate warheads. While the JAK3 inhibitors failed to achieve covalent binding, the fluorosulfate-bearing MK2 inhibitor 42, which had been designed as an allosteric binder, unexpectedly formed a bond with the "catalytic" lysine, additionally uncovering a unique interaction at the hinge region. This highlights the untapped potential of fluorosulfates and provides a rare example of the use of this electrophile for lysine targeting in kinases. Our results highlight the limitations of traditional design methods and support the integration of fragment/lead-like covalent library screening to discover unanticipated interactions.

RSC Medicinal ChemistryVol. 16(10)
Goethe University Frankfurt (DE), University of Eastern Finland (FI), German Cancer Research Center (DE), Heidelberg University (DE), Frankfurt Institute for Advanced Studies (DE), German Center for Infection Research (DE), University of Tübingen (DE)
Bristol-Myers Squibb, Pfizer, Bayer, Baden-Württemberg Stiftung, McGill University, Deutsches Krebsforschungszentrum, Genome Canada, Deutsches Zentrum für Infektionsforschung, Evonik Stiftung, European Federation of Pharmaceutical Industries and Associations, Deutsche Forschungsgemeinschaft, Eberhard Karls Universität Tübingen, Studienstiftung des Deutschen Volkes, China Scholarship Council, Deutsche Krebshilfe, Innovative Medicines Initiative, Deutschen Konsortium für Translationale Krebsforschung
Openalex Percentile: Top 72%
Cytokine Signaling Pathways and Interactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.