James McDonnell

Professor

King’s College London

United Kingdom

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James McDonnell is a Professor at King's College London, specializing in antibody structure and function. His recent research focuses on the crystal structures of human immunoglobulins and their implications in various antibody isotypes. Additionally, he investigates the glycosylation of IgE and develops innovative diagnostic tools in immunology. Based in the United Kingdom, he contributes significantly to the understanding of innate immunity and therapeutic strategies in cancer.

Articles (12)

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2025

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2024

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2020

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2020

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2020

Collaborators (8)

Kim Wolff

King’s College London

UNITED KINGDOM

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Anna Marie Davies

King’s College London

UNITED KINGDOM

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Alicia Michelle Chenoweth

King’s College London

UNITED KINGDOM

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Paul Royall

King’s College London

UNITED KINGDOM

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Mariangela Figini

Fondazione IRCCS Istituto Nazionale dei Tumori

ITALY

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Hassan Morad

Lecturer in Immunology

University of Westminster

UNITED KINGDOM

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Alkistis Mitropoulou

University College London

UNITED KINGDOM

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Sophia Karagiannis

King’s College London

UNITED KINGDOM

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James McDonnell

Research Interests

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About

Articles (12)

The Crystal Structure of Human IgD-Fc Reveals Unexpected Differences With Other Antibody Isotypes

IgE glycosylation and impact on structure and function: A systematic review

Crystal structures of the human IgD Fab reveal insights into CH1 domain diversity

IgE, IgE Receptors and Anti-IgE Biologics: Protein Structures and Mechanisms of Action

Expanding the Anti-Phl p 7 Antibody Toolkit: An Anti-Idiotype Nanobody Inhibitor

Generation and Characterization of Native and Sialic Acid-Deficient IgE

Development of a point‐of‐care test for the detection of MDMA in latent fingerprints using surface plasmon resonance and lateral flow technology

Reviving lost binding sites: Exploring calcium-binding site transitions between human and murine CD23.

Nucleolin acts as the receptor for C1QTNF4 and supports C1QTNF4-mediated innate immunity modulation

Engineering the Fab fragment of the anti-IgE omalizumab to prevent Fab crystallization and permit IgE-Fc complex crystallization.

Rapid conjugation of antibodies to toxins to select candidates for the development of anticancer Antibody-Drug Conjugates (ADCs)

NMR backbone assignment of the Cε4 domain of immunoglobulin E

Collaborators (8)

Kim Wolff

Anna Marie Davies

Alicia Michelle Chenoweth

Paul Royall

Mariangela Figini

Hassan Morad

Alkistis Mitropoulou

Sophia Karagiannis

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