Author

Tomas B. Voisin

The Francis Crick InstituteORCID 0000-0003-0697-8563Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Assay:cryo-EM· 1 Research Focus:protein folding & dynamics· 1 Assay:proteomics· 1

Frequent Co-Authors

David BalchiniD· 2 shared Grant A. PelloweiD· 2 shared Laura KarpauskaiteiD· 2 shared Mark J. SkeheliD· 2 shared Sarah MasleniD· 2 shared Alžběta RoeselováiD· 1 shared Andrea NansiD· 1 shared Chloë RoustaniD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersBiochemistry

David BalchinORCID

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2 papers

Recent·Most cited

Molecular determinants of cotranslational chaperone recruitment to nascent p53

Laura Karpauskaite, Tomas B. Voisin, Sarah Maslen, Lois Kent, Grant A. Pellowe, Mark J. Skehel, David Balchin

The paper investigates how chaperones like Hsp70, Hsp90, and TRiC bind to nascent p53 during translation, showing TRiC's specificity and how mutations affect this process.

bioRxiv · Apr 21, 2026 · PreprintBiochemistry

The human ribosome modulates multidomain protein biogenesis by delaying cotranslational domain docking

Grant A. Pellowe, Tomas B. Voisin, Laura Karpauskaite, Sarah Maslen, Alžběta Roeselová, Mark J. Skehel, Chloë Roustan, Roger George, Andrea Nans, Svend Kjær, Ian A. Taylor, David Balchin

The paper investigates how the human ribosome modulates multidomain protein folding by delaying domain docking, contrasting with bacterial ribosomes.

Nature Structural & Molecular Biology · Sep 19, 2025Peer-reviewedBiochemistry