Synopsis
Protein turnover is crucial in maintaining cellular homeostasis and this process is largely controlled by the Ubiquitin Proteasome Pathway (UPP). The pathway consists of an enzymatic cascade that links the polypeptide cofactor Ubiquitin to specific protein targets, which mark them for degradation by the proteasome. This cascade is highly regulated and impacts virtually all cellular processes including cell cycle progression, cell proliferation, cell differentiation and apoptosis. Malfunction of the UPP has been implicated in the development of diseases such as cancer, immune disorders and neurodegeneration.
The ability to understand and manipulate the UPP is a major objective in being able to manage disease biology. While the validity of this approach was first exemplified by the proteasome inhibitor bortezomib, approved by the FDA in 2003 and used in the treatment of multiple myeloma and mantle cell lymphoma, subsequent advances in understanding the role of different components in the UPP have allowed the development of other high quality chemical probes and inhibitors.
This meeting aims to showcase recent innovations by scientists working in both academia and industry in this exciting and rapidly expanding field.
Programme
Event Day - 19 May 2017
Day's schedule
- 10:00
- Registration and refreshments
- 10:25
- Opening remarks
- 10:30
- PROTACs: Induced Protein Degradation as a Therapeutic Strategy Craig Crews, Yale Center for Molecular Discovery
- 11:30
- Ubiquitin system modulation: strategies and technologies Satpal Virdee, University of Dundee
- 12:00
- Chemical Ubiquitination Huib Ovaa, Leiden University Medical Centre
- 12:30
- Lunch and exhibiton
- 14:00
- From Pan-Kinase Promiscuity to Selective Degradation using PROTACs Christopher Tinworth, GlaxoSmithKline
- 14:30
- Inhibitors of the E2 ubiquitin conjugating enzyme Rad6: discovery and anticancer properties Andrew Westwell, Cardiff University
- 15:00
- Refreshments and exhibition
- 15:30
- Enabling and supporting ubiquitin system targeted drug discovery Jason Brown, Ubiquigent
- 16:00
- Ubiquitin -Omics for Target Discovery in Human Disease Benedikt Kessler, Nuffield Department of Medicine
- 16:30
- Protein Degradation by In-Cell Self-Assembly of Proteolysis Targeting Chimeras Tom Heightman, Astex Pharmaceuticals
- 17:00
- Closing remarks and conference close.
Venue and Contact
Fees
Early bird fees before Tuesday 18 April 2017
GB£80 . . . . . . . . . . . . . . . . . SCI Member
GB£35 . . . . . . . . . . . . . . . . . SCI Student Member
GB£50 . . . . . . . . . . . . . . . . . SCI Subsidised Member
GB£120 . . . . . . . . . . . . . . . . Non-Member
Standard fees after Tuesday 18 April 2017
GB£130 . . . . . . . . . . . . . . . . SCI Member
GB£50 . . . . . . . . . . . . . . . . . SCI Student Member
GB£70 . . . . . . . . . . . . . . . . . SCI Subsidised Member
GB£170 . . . . . . . . . . . . . . . . Non-Member
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Keynote speaker
Craig Crews, Yale Center for Molecular Discovery
PROTACs: Induced Protein Degradation as a Therapeutic Strategy