Matthew James Stewart, PhD

Postdoctoral Associate in Pharmacology

About

Postdoctoral Associate in Pharmacology

PhD: University of Birmingham, Institute of Cancer and Genomic Sciences/Cancer and Genomic Sciences (2025)

MSc: University of Leicester, Institute for Structural and Chemical Biology/Cancer Cell and Molecular Biology (2017)

BSc (Hon): University of Leicester, Institute for Structural and Chemical Biology/Medical Biochemistry (2016)

MDC1 mediates Pellino recruitment to sites of DNA double-strand breaks.
Torres Esteban M, Stewart MJ, Bragginton E, Meroni A, Pellizzari A, Jeanrenaud A, Smerdon SJ, Stucki M. MDC1 mediates Pellino recruitment to sites of DNA double-strand breaks. Life Sci Alliance 2025, 8 PMID: 40049731, DOI: 10.26508/lsa.202403074.
Peer-Reviewed Original Research

Thermostability-based binding assays reveal complex interplay of cation, substrate and lipid binding in the bacterial DASS transporter, VcINDY.
Sampson CDD, Fàbregas Bellavista C, Stewart MJ, Mulligan C. Thermostability-based binding assays reveal complex interplay of cation, substrate and lipid binding in the bacterial DASS transporter, VcINDY. Biochem J 2021, 478: 3847-3867. PMID: 34643224, DOI: 10.1042/BCJ20210061.
Peer-Reviewed Original Research

Solvent accessibility changes in a Na(+)-dependent C(4)-dicarboxylate transporter suggest differential substrate effects in a multistep mechanism.
Sampson CDD, Stewart MJ, Mindell JA, Mulligan C. Solvent accessibility changes in a Na(+)-dependent C(4)-dicarboxylate transporter suggest differential substrate effects in a multistep mechanism. J Biol Chem 2020, 295: 18524-18538. PMID: 33087444, DOI: 10.1074/jbc.RA120.013894.
Peer-Reviewed Original Research

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