Award details

A quantitative biomolecular interaction suite

Reference	BB/L013851/1
Principal Investigator / Supervisor	Professor Stuart Wilson
Co-Investigators / Co-Supervisors	Professor Kathryn Ayscough, Professor Bazbek Davletov, Dr Kai Sven Erdmann, Professor Jane Grasby, Professor J Green, Professor Dave Kelly, Dr Stéphane MESNAGE, Dr Andrew Peden, Professor Robert K Poole
Institution	University of Sheffield
Department	Molecular Biology and Biotechnology
Funding type	Research
Value (£)	223,658
Status	Completed
Type	Research Grant
Start date	01/12/2013
End date	30/11/2014
Duration	12 months

Abstract

The accurate quantitative measurement of biomolecular interactions is an important aspect of modern molecular biology research. Such quantitation will ultimately allow us to build accurate models for a variety of biological process. In this proposal we will establish a facility which makes use of two distinct biophysical techniques to quantitate biomolecular interactions: 1) isothermal titration calorimetry (ITC) and 2) microscale thermophoresis (MT). The facility will chiefly comprise of a Microcal ItC200 machine and a Nanotemper Monolith NT.115 machine. These two machines each have distinctive features and the combination of the two biophysical techniques they employ will provide a world class facility for biomolecular interaction analysis. The facility will be open to both internal and external users and will allow biomolecular interaction quantification using completely unlabelled samples in solution (using ITC). Alternatively using MT, investigators will be able to measure biomolecular interactions in complex mixtures such as cell lysates, where one of the biomolecules is fluorescently labelled. The exquisite sensitivity of MT means that quantitative measurements will be accessible even for very large proteins or complexes, which are frequently difficult to purify in sufficient quantities for ITC work. The applicants will utilise this facility to quantitate a wide range of biomolecular interactions including: the analysis of TREX mRNA complex assembly, membrane trafficking, nucleases, bacterial cell wall structure, actin binding proteins, novel protein linking technologies, cAMP and nitric oxide signalling, protein secretion, carbon monoxide releasing molecules and defense mechanisms of bacterial pathogens.

Summary

Proteins in living organisms frequently interact with each other and with DNA, RNA and small molecules. In order to be able to understand how all these interactions help an organisms to survive and build models for these interactions, it is important to be able to measure the interactions in a quantitative way. In this proposal we will establish a facility which will house two separate machines which use different biophysical methods to accurately measure interactions between molecules found in biology. We will use these machines to carry out a wide variety of research ranging from how complexes of proteins assemble to how the walls of bacterial cells work.

Impact Summary

(A) Potential Beneficiaries Beneficiaries of the research will be academics, health professionals, industry and schools. (B) How might they benefit ? (i) Academic Beneficiaries will be post-doctoral researchers, PhD students and technicians from a wide range of disciplines including biochemists, through cell biologists to systems biologists, chemists and molecular biologists. They will receive high quality training from the PIs and technicians associated with this facility. They will also publish high quality high impact publications including reviews. Reviews will ensure coverage not just to those in the immediate field, but to a broader audience of biologists at a range of academic levels. Work at this level enhances the reputation of UK science in general and this is key to confidence in the competitiveness of UK, which is directly related to wealth and economic output of the higher education industry. Timescale 1-5 years. (ii) Health related disciplines will benefit from this study. The quantitative studies proposed in this project will provide a better understanding of the biomolecular interactions which impinge on a range of human disorders and this provides the opportunity to impact on the treatment of these disorders in the future. These conditions include: Neuromuscular and neurodegenerative disorders, cancer, microbial infections, chronic pain and acromegaly. Timescale 2-5 years. (iii) Industry. Typically drugs which target the range of diseases and infections described above require small molecule inhibitors. This project will allow us to make detailed quantitative measurements of small molecule interactions with other biomolecules and such measurements will impact on the design in the pharmaceutical industry of suitable drugs for treatment of such disorders and infections. Small molecules which associate with biomolecules might also be used in the biotechnology, agriculture and engineering industries and the work proposed here with this facility will aid in the design of such useful molecules for these industries. In addition the post-docs, PhD students and technicians trained in the laboratories involved may well enter industry and carry out much of the research and development in the future. Our ability to supply highly trained scientists will positively impact on the ability of the UK industrial sector to remain competitive. Timescale 2-5 years. (iv) Schools. The future of science depends on enthusiastic young scientists. The best way to achieve this is to provide stimulating scientific based activities for school children. Several of the applicants are involved in visiting schools to give talks and run activities. Timescale: Schools are visited on an annual basis.

Committee	Research Committee C (Genes, development and STEM approaches to biology)
Research Topics	Structural Biology
Research Priority	X – Research Priority information not available
Research Initiative	Advanced Life Sciences Research Technology Initiative (ALERT) [2013-2014]
Funding Scheme	X – not Funded via a specific Funding Scheme

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