05:46am Wednesday 20 September 2017

Controlling the ‘social life’ of proteins aims to transform drug discovery

The new project, which will launch on 1 February 2016, will involve researchers from the University of Leeds, the University of Bristol and three drug discovery organisations: the Northern Institute for Cancer Research, Newcastle University; AstraZeneca; and Domainex.

Professor Andrew Wilson, Deputy Director of The Astbury Centre at the University of Leeds, who will lead the project, said: “This is a huge untapped opportunity. There are thought to be as many as 600,000 protein-protein interactions that could be targets for new drugs. But we don’t know which ones are most important, what is crucial for their interaction and how to target them. If we can develop our understanding of this ‘social life’ of proteins, significant strides could be made in drug discovery.

“Our project will create the tools to make this kind of drug discovery easier by analysing and categorising the important features of protein-protein interactions. This will provide the basis for discovering many new drugs for the treatment of disease.”

To develop new drugs, scientists have become adept at blocking well-defined binding sites on proteins where small molecules can bind. This allows, for instance, many enzymes – a type of protein that accelerates a chemical reaction – involved in disease processes to be disabled.

Dr Gail Bartlett, who will lead the computational biochemistry research at Bristol, explained the greater challenge of disrupting protein-protein interactions. “A protein-protein interaction is more like a handshake or an embrace. We don’t know which chemical and structural features of the interface are most important, and additionally, the characteristics of small molecules that could block them are largely unknown. This project will elucidate rules for designing small molecules to target these interfaces.”

Professor Adam Nelson, also from the University of Leeds, concluded: “Increasing innovation in drug discovery is a major challenge, in part because the easier, ‘low-hanging’ drug targets have already been largely tapped. Our research will pave the way for a wide range of protein-protein interactions to be targeted by drugs in future.”

The five-year project is being funded by the Engineering and Physical Sciences Research Council (EPSRC).


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