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Publications

Accelerating drug target inhibitor discovery with a deep generative foundation model.

Chenthamarakshan V. et al, (2023), Science advances, 9

Bacteriophage PRD1 as a nanoscaffold for drug loading.

Duyvesteyn HME. et al, (2021), Nanoscale

Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum

Liu C. et al, (2021), Cell, 184, 4220 - 4236.e13

Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera

Zhou D. et al, (2021), Cell, 184, 2348 - 2361.e6

Reduced neutralization of SARS-CoV-2 B.1.1.7 variant by convalescent and vaccine sera

Supasa P. et al, (2021), Cell, 184, 2201 - 2211.e7

The antigenic anatomy of SARS-CoV-2 receptor binding domain

Dejnirattisai W. et al, (2021), Cell, 184, 2183 - 2200.e22

Glutathione facilitates enterovirus assembly by binding at a druggable pocket.

Duyvesteyn HME. et al, (2020), Communications biology, 3

Glutathione facilitates enterovirus assembly by binding at a druggable pocket.

Duyvesteyn HME. et al, (2020), Communications biology, 3

Phage G Structure at 6.1 Å Resolution, Condensed DNA, and Host Identity Revision to a Lysinibacillus

González B. et al, (2020), Journal of Molecular Biology

A structural basis for antibody-mediated neutralization of Nipah virus reveals a site of vulnerability at the fusion glycoprotein apex.

Avanzato VA. et al, (2019), Proceedings of the National Academy of Sciences of the United States of America, 116, 25057 - 25067

Assembly of complex viruses exemplified by a halophilic euryarchaeal virus

De Colibus L. et al, (2019), Nature Communications, 10

The structure of a prokaryotic viral envelope protein expands the landscape of membrane fusion proteins

El Omari K. et al, (2019), Nature Communications, 10

Author Correction: Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Walters LC. et al, (2018), Nature Communications, 9

Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Walters LC. et al, (2018), Nature Communications, 9

Near-atomic structure of Japanese encephalitis virus reveals critical determinants of virulence and stability

Wang X. et al, (2017), Nature Communications, 8

High-speed fixed-target serial virus crystallography

Roedig P. et al, (2017), Nature Methods, 14, 805 - 810

Potent neutralization of hepatitis A virus reveals a receptor mimic mechanism and the receptor recognition site

Wang X. et al, (2017), Proceedings of the National Academy of Sciences, 114, 770 - 775

Structure of human Aichi virus and implications for receptor binding

Zhu L. et al, (2016), Nature Microbiology, 1

The crystal structure of human dopamine β-hydroxylase at 2.9 Å resolution

Vendelboe TV. et al, (2016), Science Advances, 2

A RANKL mutant used as an inter-species vaccine for efficient immunotherapy of osteoporosis

Liu C. et al, (2015), Scientific Reports, 5

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