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Clock proteins and their interactions in the zebrafish circadian system
Reference
BBS/B/02886
Principal Investigator / Supervisor
Professor David Whitmore
Co-Investigators /
Co-Supervisors
Institution
University College London
Department
Cell and Developmental Biology
Funding type
Research
Value (£)
335,211
Status
Completed
Type
Research Grant
Start date
06/08/2004
End date
05/08/2007
Duration
36 months
Abstract
Our understanding of the cellular circadian clock mechanism has progressed dramatically through the use of genetic approaches in Drosophila and mouse. However, as tissue is limiting in these systems, biochemical studies are often difficult to perform. This problem has been overcome in zebrafish, where we have produced several light responsive, clock-containing cell lines. These cells are a unique system for clock analysis, in that, for the first time, the amount of starting material is not limiting. The aim of this proposal is to employ large-scale proteomic approaches to analyse clock proteins, using antibodies to study their expression and localisation, and affinity purification to study the interactions and complexes they form.
Summary
unavailable
Committee
Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
Proteomics and Cell Function (PCF) [2003-2004]
Funding Scheme
X – not Funded via a specific Funding Scheme
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