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Probing nascent peptide: ribosome exit tunnel interactions
Reference
C20418
Principal Investigator / Supervisor
Dr Jeremy Brown
Co-Investigators /
Co-Supervisors
Professor Martin Ryan
Institution
Newcastle University
Department
School of Cell and Molecular Biosciences
Funding type
Research
Value (£)
194,320
Status
Completed
Type
Research Grant
Start date
01/01/2004
End date
31/12/2006
Duration
36 months
Abstract
The FMDV 2A peptide catalyses co-translational cleavage at its own C-terminus in eukaryotic cells. This project aims to understand the mechanism of this intra-ribosomal polypeptide scission reaction. Using the observation that 2A is active in the genetically tractable S .cerevisiae we will undertake screens to establish both critical features of 2A that contribute to, and host cell factors that are required for, cleavage. Further, based on similarity between 2A and bacterial peptides that cause translation we will undertake experiments to identify 2A variants that function in the context of prokaryotic cells. Finally we will establish conditions for trapping and purifying ribosomes containing 2A thereby opening the door to structural studies. (Joint with grant number 20035).
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
X - not in an Initiative
Funding Scheme
X – not Funded via a specific Funding Scheme
Associated awards:
C20035 Probing nascent peptide: ribosome exit tunnel interactions
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