p21-Activated Kinase (PAK) Group I-Targeting Inhibitors Promote the Dimeric Conformation in Live Cells

High Resolution Image Download MS PowerPoint Slide p21-activated kinases (PAKs) are involved in a broad range of cellular processes and are emerging drug targets. The human PAK family consists of 6 kinases, divided into group I (PAK1-3) and group II (PAK4-6), both families are regulated by distinct activation mechanisms and interaction partners. Currently, there are no assays available enabling the study of on-target activity for all PAK isoforms in cells. To this end, we developed a series of NanoLuc- and HaloTag-based bioluminescence resonance energy transfer assays to quantify inhibitor target engagement and dimerization of PAK isoforms in living cells. Interestingly, we found evidence that inhibitors might promote the formation of group I PAK dimers. Thus, our data uncovered a live-cell mechanism by which inhibitors modulate this dimeric conformation and provide new tools for future PAK inhibitor design.

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Journal
ACS Chemical Biology
Published
2026-06-13
DOI
https://doi.org/10.1021/acschembio.6c00410
Primary Topic
Protein Kinase Regulation and GTPase Signaling
Type
article
Field-Weighted Citation Impact
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article

p21-Activated Kinase (PAK) Group I-Targeting Inhibitors Promote the Dimeric Conformation in Live Cells

Benedict‐Tilman Berger, Viktoria Morasch, Martin P. Schwalm, Susanne Müller et al.
ACS Chemical Biology
Protein Kinase Regulation and GTPase Signaling
article

p21-Activated Kinase (PAK) Group I-Targeting Inhibitors Promote the Dimeric Conformation in Live Cells

Benedict‐Tilman Berger, Viktoria Morasch, Martin P. Schwalm, Susanne Müller, T. Matos, Lewis Elson, Andreas Krämer, Theresa A. L. Ehret, Nicolai D. Raig, Felix Nowotka, Stefan Knapp, Neele Manik
article en

Abstract

High Resolution Image Download MS PowerPoint Slide p21-activated kinases (PAKs) are involved in a broad range of cellular processes and are emerging drug targets. The human PAK family consists of 6 kinases, divided into group I (PAK1-3) and group II (PAK4-6), both families are regulated by distinct activation mechanisms and interaction partners. Currently, there are no assays available enabling the study of on-target activity for all PAK isoforms in cells. To this end, we developed a series of NanoLuc- and HaloTag-based bioluminescence resonance energy transfer assays to quantify inhibitor target engagement and dimerization of PAK isoforms in living cells. Interestingly, we found evidence that inhibitors might promote the formation of group I PAK dimers. Thus, our data uncovered a live-cell mechanism by which inhibitors modulate this dimeric conformation and provide new tools for future PAK inhibitor design.

ACS Chemical Biology
Goethe University Frankfurt (DE), German Cancer Research Center (DE), Heidelberg University (DE), Universidade Federal do Ceará (BR), PharmacoGenetics (China) (CN)
Affordable and clean energy
Openalex Percentile: Top 9%
Protein Kinase Regulation and GTPase Signaling
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