Unit Director

Molecular basis for inherited mitochondrial disease

Deputy Director

Understanding the molecular mechanism of complex I and its roles in human disease

Programme Leader

Mitochondrial genomics and human diseases

Mass Spectrometry Facility

Identifying and characterising mitochondrial proteins and their associations

Programme Leader

Understanding transport processes in mitochondria

Programme Leader

Discovering the genetic links between mitochondrial dysfunction and human disease

Programme Leader

Targeting therapeutic and probe molecules to mitochondria, mitochondrial radical production and redox signalling

Bioinformatics Facility

Understanding mitochondria using computer modelling

Programme Leader

Genetic models of neurodegenerative disease

Emeritus Director

Understanding the molecular mechanism of how ATP is made