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Publications

Bacteriophage PRD1 as a nanoscaffold for drug loading.

Duyvesteyn HME. et al, (2021), Nanoscale

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

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

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

Zhou D. et al, (2021), Cell

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

Supasa P. et al, (2021), Cell

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, 432, 4139 - 4153

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

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, e1500980 - e1500980

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

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

The Human Otubain2-Ubiquitin Structure Provides Insights into the Cleavage Specificity of Poly-Ubiquitin-Linkages

Altun M. et al, (2015), PLOS ONE, 10, e0115344 - e0115344

More-powerful virus inhibitors from structure-based analysis of HEV71 capsid-binding molecules

De Colibus L. et al, (2014), Nature Structural & Molecular Biology, 21, 282 - 288

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