User:Cameron Neylon: Difference between revisions
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University of Southampton<br> | |School of Chemistry<br>University of Southampton<br>Southampton<br>SO17 1BJ, UK||ISIS Neutron Facility<br>STFC Rutherford Appleton Laboratory<br>Chilton, Didcot<br>OX11 0QX, UK | ||
Southampton<br> | |||
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I am a Lecturer in Chemical Biology at the School of Chemistry at the University of Southampton with a joint appointment at the ISIS Pulsed Neutron Source, Rutherford Appleton Laboratory, near Oxford. The group at Southampton works in the areas of protein-ligand binding and directed evolution with a focus on methods development for high throughput analysis and protein labeling. | {|style="width:100%; height:450px" | ||
|I am a Lecturer in Chemical Biology at the School of Chemistry at the University of Southampton with a joint appointment at the ISIS Pulsed Neutron Source, Rutherford Appleton Laboratory, near Oxford. The group at Southampton works in the areas of protein-ligand binding <cite> cell06 mmbr05 biochem00 </cite> and directed evolution <cite>nar04</cite>with a focus on methods development for high throughput analysis and protein labeling<cite>bioconjchem04</cite>. We have recently developed methodology for the immobilisation of proteins on solid supports as well as the site selective fluorescent labelling of proteins. I am also involved in the 4G Basic Technology project which is developing encoded microparticles for use in high throughput assays. The project has demonstrated the feasibility of encoding manufactured particles using minature diffraction gratings, the ability to carry out multistep synthesis on these particles <cite> jcombchem07 </cite>, as well as performing multiplexed immunoassays and DNA hybridisation. We have also analysed the ability of high throughput DNA sequencing <cite>nar06</cite> to deliver useful information and developed new tools for designing hybridisation probes for DNA analysis <cite>natphys05</cite>. | |||
At the Rutherford Laboratory we are developing and promoting neutron and X-ray scattering techniques for applications in the biological sciences. Scattering techniques provide a means of obtaining low resolution information on biomolecules in solution. It is particularly useful in determining the structure of biomolecular complexes in solution, especially where high resolution structural data is available on the individual components of the complex. | |||
The combination of high throughput methodology and working on two sites has led to a developing programme in e-science particularly in the area of electronic lab notebooks. In collaboration with the e-science group at Southampton and Jeremy Frey we are developing and testing an electronic notebook based on a blog. This has the potential to provide a very flexible framework for recording and analysing data but is currently at an early stage of development. | |||
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== Research Interests == | == Research Interests == | ||
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Revision as of 06:17, 30 April 2007
Cameron Neylon
Research Interests
References
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