Biography
Brian completed his BSc in Chemistry (Hons) at the National University of Ireland Galway. He then spent two years working as a Synthetic Chemist for an early stage R+D pharmaceutical company synthesising novel oncology drugs in Sydney, Australia.
He then undertook his PhD studies at the University of Sydney with Prof Roger Truscott where his research focused on the age-related changes that occur in long-lived human proteins and the implications these have for Alzheimer’s disease and multiple sclerosis.
As a postdoctoral researcher within the Davis group (Chemistry, University of Oxford) he worked on a variety of projects all of which were based on modifying viruses, proteins sugars and antibodies to understand, exploit and modify biomolecular function.
While working with Prof Len Seymour (Oncology, University of Oxford) he began applying these skills in a more translational manner to chemically modify oncolytic viruses in order to increase tumour penetration via ultrasound mediated propulsion.
Now as Senior Research Fellow working in the BUBBL group he is primarily developing novel immune stimulating cavitation agents to enhance the potency and tumour specific targeting of cancer immunotherapies.
Most Recent Publications
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Monitoring the disassembly of virus-like particles by (19)F-NMR
Monitoring the disassembly of virus-like particles by (19)F-NMR
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption
Research Interests
- Design, formulation and characterisation of immune stimulating cavitation nuclei
- Transdermal delivery of drugs and vaccines
- Synthesis of immune modulating nanoparticles and vaccine formulations
- Developing tumour specific targeting strategies for cancer immunotherapies
Research Funding received from:
- OXCD3
- TherOximmune
- John Fell Research Fund
- Cancer Research Development Fund
Research Groups
Related Academics
Most Recent Publications
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Monitoring the disassembly of virus-like particles by (19)F-NMR
Monitoring the disassembly of virus-like particles by (19)F-NMR
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption
Publications
Most Recent Publications
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Bi- and tri-valent T cell engagers deplete tumour-associated macrophages in cancer patient samples
Monitoring the disassembly of virus-like particles by (19)F-NMR
Monitoring the disassembly of virus-like particles by (19)F-NMR
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Spontaneous cleavage of proteins at serine and threonine is facilitated by zinc
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Amyloid Plaque in the Human Brain Can Decompose from Aβ(1-40/1-42) by Spontaneous Nonenzymatic Processes
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption
Dysregulation of inter-photoreceptor retinoid-binding protein (IRBP) after induced Müller cell disruption