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Targeting anisomycin receptors: a chemical biology approach

ReferenceB20011
Principal Investigator / Supervisor Professor Alison Hulme
Co-Investigators /
Co-Supervisors
Institution University of Edinburgh
DepartmentSch of Chemistry
Funding typeResearch
Value (£) 124,114
StatusCompleted
TypeResearch Grant
Start date 01/02/2004
End date 31/01/2006
Duration24 months

Abstract

The precise target of action of the pyrrolidine antibiotic anisomycin which activates the mitogen-activated protein (MAP) JNK and p38 stress kinase (SAPK) pathways in mammalian, yeast, or insect cells has not been elucidated. As biochemical and genetic studies demonstrate that the SAPK pathways regulate cell proliferation, differentiation and cell repair/apoptosis, studies into the mechanism of initiation and regulation of these pathways may provide new leads for therapeutic targets. the chemical synthesis of biotinylated molecular probes and photoactivatable molecular probes based on recent anisomycin analogues should allow the future isolation of the anisomycin receptor and produce information relating to targets upstream of the MAPKKs.

Summary

unavailable
Committee Closed Committee - Biomolecular Sciences (BMS)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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