Nature Communications (Oct 2022)
A selective and orally bioavailable VHL-recruiting PROTAC achieves SMARCA2 degradation in vivo
- Christiane Kofink,
- Nicole Trainor,
- Barbara Mair,
- Simon Wöhrle,
- Melanie Wurm,
- Nikolai Mischerikow,
- Michael J. Roy,
- Gerd Bader,
- Peter Greb,
- Géraldine Garavel,
- Emelyne Diers,
- Ross McLennan,
- Claire Whitworth,
- Vesna Vetma,
- Klaus Rumpel,
- Maximilian Scharnweber,
- Julian E. Fuchs,
- Thomas Gerstberger,
- Yunhai Cui,
- Gabriela Gremel,
- Paolo Chetta,
- Stefan Hopf,
- Nicole Budano,
- Joerg Rinnenthal,
- Gerhard Gmaschitz,
- Moriz Mayer,
- Manfred Koegl,
- Alessio Ciulli,
- Harald Weinstabl,
- William Farnaby
Affiliations
- Christiane Kofink
- Boehringer Ingelheim RCV GmbH & Co KG
- Nicole Trainor
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Barbara Mair
- Boehringer Ingelheim RCV GmbH & Co KG
- Simon Wöhrle
- Boehringer Ingelheim RCV GmbH & Co KG
- Melanie Wurm
- Boehringer Ingelheim RCV GmbH & Co KG
- Nikolai Mischerikow
- Boehringer Ingelheim RCV GmbH & Co KG
- Michael J. Roy
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Gerd Bader
- Boehringer Ingelheim RCV GmbH & Co KG
- Peter Greb
- Boehringer Ingelheim RCV GmbH & Co KG
- Géraldine Garavel
- Boehringer Ingelheim RCV GmbH & Co KG
- Emelyne Diers
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Ross McLennan
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Claire Whitworth
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Vesna Vetma
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Klaus Rumpel
- Boehringer Ingelheim RCV GmbH & Co KG
- Maximilian Scharnweber
- Boehringer Ingelheim RCV GmbH & Co KG
- Julian E. Fuchs
- Boehringer Ingelheim RCV GmbH & Co KG
- Thomas Gerstberger
- Boehringer Ingelheim RCV GmbH & Co KG
- Yunhai Cui
- Boehringer Ingelheim Pharma GmbH & Co KG
- Gabriela Gremel
- Boehringer Ingelheim RCV GmbH & Co KG
- Paolo Chetta
- Boehringer Ingelheim RCV GmbH & Co KG
- Stefan Hopf
- Boehringer Ingelheim RCV GmbH & Co KG
- Nicole Budano
- Boehringer Ingelheim RCV GmbH & Co KG
- Joerg Rinnenthal
- Boehringer Ingelheim RCV GmbH & Co KG
- Gerhard Gmaschitz
- Boehringer Ingelheim RCV GmbH & Co KG
- Moriz Mayer
- Boehringer Ingelheim RCV GmbH & Co KG
- Manfred Koegl
- Boehringer Ingelheim RCV GmbH & Co KG
- Alessio Ciulli
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- Harald Weinstabl
- Boehringer Ingelheim RCV GmbH & Co KG
- William Farnaby
- Centre for Targeted Protein Degradation, School of Life Sciences, University of Dundee
- DOI
- https://doi.org/10.1038/s41467-022-33430-6
- Journal volume & issue
-
Vol. 13,
no. 1
pp. 1 – 15
Abstract
Protein degraders are an emerging drug modality; however, their properties lie beyond typical drug-like space. Here the authors report optimisation via structure-based exit vector and linker design towards the VHL-recruiting PROTAC ACBI2, an orally bioavailable and selective degrader of SMARCA2.