Edmund Kunji

Professor of Biophysics

University of Cambridge

United Kingdom

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Professor Edmund Kunji is a faculty member in the Department of Biophysics at the University of Cambridge, UK. His research primarily focuses on the biophysics of mitochondrial carriers, including the SLC25 family, and the mechanisms underlying pyruvate transport, as well as related pathogenic mechanisms in Citrin deficiency. He has authored several recent articles that explore topics such as proton conductance, acyltransferases regulating phospholipid composition, and the kinetic mechanisms of substrate exchange in mitochondrial carriers.

Articles (20)

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2025

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2025

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2025

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2025

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2025

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2024

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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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2022

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2022

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2022

Collaborators (12)

Thomas Zögg

Vrije Universiteit Brussel

BELGIUM

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Paul Crichton

Professor at University of East Anglia

University of East Anglia

UNITED KINGDOM

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Shane Palmer

MRC Biostatistics Unit

UNITED KINGDOM

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Bert Poolman

Professor of Biochemistry

University of Groningen

NETHERLANDS

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Vanessa Leone

Assistant Professor

Medical College of Wisconsin

UNITED STATES

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Johannes Häberle

University of Zurich

SWITZERLAND

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Els Pardon

Vrije Universiteit Brussel

BELGIUM

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Vladimir Hampl

Charles University

CZECH REPUBLIC

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Jan Steyaert

Vrije Universiteit Brussel

BELGIUM

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Denis Lacabanne

UNITED KINGDOM

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Georgios Makris

University of Zurich

SWITZERLAND

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Michael Murphy

Professor of Mitochondrial Redox Biology

University of Cambridge

UNITED KINGDOM

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Edmund Kunji

Research Interests

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Articles (20)

Deciphering the Mutational Background in Citrin Deficiency Through a Nationwide Study in Japan and Literature Review

Proton conductance by human uncoupling protein 1 is inhibited by purine and pyrimidine nucleotides

TRAM–LAG1–CLN8 family proteins are acyltransferases regulating phospholipid composition

Molecular basis of pyruvate transport and inhibition of the human mitochondrial pyruvate carrier

Synthetic syntrophy for adenine nucleotide cross-feeding between metabolically active nanoreactors

The peculiar properties of mitochondrial carriers of the SLC25 family

Current Understanding of Pathogenic Mechanisms and Disease Models of Citrin Deficiency

Human mitochondrial carriers of the SLC25 family function as monomers exchanging substrates with a ping-pong kinetic mechanism

Structural mechanisms of mitochondrial uncoupling protein 1 regulation in thermogenesis

Membrane potential stimulates ADP import and ATP export by the mitochondrial ADP/ATP carrier due to its positively charged binding site

Structural basis of purine nucleotide inhibition of human uncoupling protein 1

Human mitochondrial ADP/ATP carrier SLC25A4 operates with a ping‐pong kinetic mechanism

Fifty years of the mitochondrial pyruvate carrier: New insights into its structure, function, and inhibition

The free-living flagellate Paratrimastix pyriformis uses a distinct mitochondrial carrier to balance adenine nucleotide pools

SLC25 family of mitochondrial transporters in GtoPdb v.2023.1

Activating ligands of Uncoupling protein 1 identified by rapid membrane protein thermostability shift analysis

Activating ligands of Uncoupling protein 1 identified by rapid membrane protein thermostability shift analysis

Pathogenic variants of the mitochondrial aspartate/glutamate carrier causing citrin deficiency

Pathogenic variants of the mitochondrial aspartate/glutamate carrier causing citrin deficiency

Substrate binding in the mitochondrial ADP/ATP carrier is a step-wise process guiding the structural changes in the transport cycle

Collaborators (12)

Thomas Zögg

Paul Crichton

Shane Palmer

Bert Poolman

Vanessa Leone

Johannes Häberle

Els Pardon

Vladimir Hampl

Jan Steyaert

Denis Lacabanne

Georgios Makris

Michael Murphy

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