Author

Dimitrios Mamalis

University of OxfordORCID 0000-0002-4396-7495Unclaimed 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 Research Focus:protein design· 1 Assay:protein sequence· 1 Assay:protein structure· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

Benjamin G. DavisiD· 2 shared Ajay JhaiD· 1 shared Andrew M. GiltrapiD· 1 shared David Bryant SaueriD· 1 shared F. von DelftiD· 1 shared Gangshun YiiD· 1 shared Huanyu Z. LiiD· 1 shared Jack Ren· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersSynthetic Biology

Benjamin G. DavisORCID

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2 papers

Recent·Most cited

Di-Gluebodies as covalently-rigidified, modular protein assemblies enable simultaneous determination of high-resolution, low-size, cryo-EM structures

Gangshun Yi, Dimitrios Mamalis, Mingda Ye, Loïc Carrique, M. Fairhead, Huanyu Z. Li, Katharina L. Duerr, Peijun Zhang, David Bryant Sauer, F. von Delft, Benjamin G. Davis, Robert J.C. Gilbert

The paper introduces Di-Gluebodies, covalently-dimerized nanobodies, to improve cryo-EM structure determination of small proteins by providing rigidity and modularity.

Nature Chemical Biology · Aug 15, 2025Peer-reviewedSynthetic Biology

Stereoretentive Post-Translational Protein Editing

Xia‐Ping Fu, Yizhi Yuan, Ajay Jha, Nikita Levin, Andrew M. Giltrap, Jack Ren, Dimitrios Mamalis, Shabaz Mohammed, Benjamin G. Davis

This paper describes a light-mediated method for stereoretentive post-translational protein editing that generates site-selectively edited proteins with full stereochemistry retention.

ACS Central Science · Feb 24, 2023Peer-reviewedSynthetic Biology