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Harry Wilders

@harrywilders.bsky.social
404 followers 1.2K following 3 posts

GSK/Francis Crick Institute Industrial Post-Doctoral Researcher exploring chemoproteomics approaches to covalent drug discovery

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Reposted by Harry Wilders
Katherine McPhie @katmcphie.bsky.social · 15/01/2025
Check out our new paper in @commschem.bsky.social, where we identified a novel enantioselective fragment for the deubiquitinating enzyme, OTUD7B. An absolute pleasure to co-lead this project with Aini Vuorinen and @cassandrakennedy.bsky.social! www.nature.com/articles/s42...
nature.com
Enantioselective OTUD7B fragment discovery through chemoproteomics screening and high-throughput optimisation - Communications Chemistry
The ovarian tumour protease (OTU) family of deubiquitinating enzymes (DUBs) are biochemically well-characterised and of therapeutic interest, however, only a few tool compounds exist to study their ce...
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Harry Wilders @harrywilders.bsky.social · 11/01/2025
Excited to see this out in Nature Communications. A great platform to profile reactive fragments against the human proteome (and beyond), quickly and accurately. #ChemBio #Chemsky
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Reposted by Harry Wilders
Adam Nelson @adam-s-nelson.bsky.social · 28/12/2024
Interested in a PhD combining high-throughput synthesis, structural and cell biology to understand kinases? Deadline to apply for a project with Richard Bayliss, Helen Matthews and me: January 6th! www.findaphd.com/phds/project...
findaphd.com
Probing covalent mechanisms of regulation and inhibition in mitotic kinases at University of Leeds on FindAPhD.com
PhD Project - Probing covalent mechanisms of regulation and inhibition in mitotic kinases at University of Leeds, listed on FindAPhD.com
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Harry Wilders @harrywilders.bsky.social · 11/12/2024
I am happy to share that our recent work has been published in Angewandte Chemie. We demonstrate how ‘direct-to-biology’ screening can accelerate optimisation campaigns, yielding potent covalent and non-covalent inhibitors from reactive fragment hits. onlinelibrary.wiley.com/doi/full/10....
onlinelibrary.wiley.com
Expedited SARS‐CoV‐2 Main Protease Inhibitor Discovery through Modular ‘Direct‐to‐Biology’ Screening
Direct-to-biology workflows promise to accelerate hit optimisation for drug discovery. Here, we describe a direct-to-biology method for the efficient synthesis and screening of cysteine-reactive frag...
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Reposted by Harry Wilders
Thorn-Seshold Lab @thornsesholdlab.bsky.social · 25/11/2024
ChemBio fans please repost the #ChemicalBiology Feed bsky.app/profile/thor... @carolynbertozzi.bsky.social @ritastrack.bsky.social @stephanhacker2.bsky.social @stuartcantrill.bsky.social @laurahowes.bsky.social @dirktrauner.bsky.social @chemjobber.bsky.social @dereklowe.bsky.social #chemsky
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