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Drug Discovery 2008

Posted: 2 August 2008 | EPR | No comments yet

Following the highly successful meeting in 2007, the European Laboratory Robotics Interest Group (ELRIG) and the Society of Biomolecular Sciences (SBS), are pleased to announce that their Drug Discovery: 2008 Meeting will be held at the Bournemouth International Centre, (BIC), UK, on 23 & 24 September 2008.

Following the highly successful meeting in 2007, the European Laboratory Robotics Interest Group (ELRIG) and the Society of Biomolecular Sciences (SBS), are pleased to announce that their Drug Discovery: 2008 Meeting will be held at the Bournemouth International Centre, (BIC), UK, on 23 & 24 September 2008.

Following the highly successful meeting in 2007, the European Laboratory Robotics Interest Group (ELRIG) and the Society of Biomolecular Sciences (SBS), are pleased to announce that their Drug Discovery: 2008 Meeting will be held at the Bournemouth International Centre, (BIC), UK, on 23 & 24 September 2008.

This conference will encompass six sessions in two days. Each will focus on a different area of Drug Discovery from selecting compounds for the corporate collection, liquid handling and detection technologies, plus advances in assay development and screening. Two sessions will address the biochemistry of two important different target classes: Enzymes and G-protein coupled receptors. Biopharmaceuticals will form the sixth session. As with the highly successful meeting in 2007, attendees will hear world class speakers discussing the challenges facing the drug discovery scientist. The scientific sessions will be complemented by plenary keynote presentations from two of the field’s foremost researchers, a poster session and a vendor exhibition with over eighty exhibitors.

Tuesday, 23 September

Drug Discovery for Enzyme Targets

Session Chairs: Andreas Sewing, Pfizer and Niall Martin, Kudos Pharma

  • Strategies for Kinase inhibitor Discovery

Ulf Boemer, Bayer

  • Inhibition of poly(ADR-ribose) polymerse – a case history

Nicola Curtin, CRUK

  • The challenges of viral enzymes as drug discovery targets

Spencer Campbell, Arrow Therapeutics

  • Shifting paradigms on enzyme- based high throughput Assays

J M Dominguez, GSK

  • Streamlined analysis of kinetics screening data – As simple as possible, but not simpler

Stephan Heyse, Genedata

Compound Management Diversifying the Corporate Collection

Session Chairs: Stephen Garland, GSK and John Morin, Wyeth

  • An Integrated Approach to Drug Discovery in the 21st Century; Working beyond our walls

Nunzio Sciammetta, Pfizer

  • Maintaining a High Quality Compound Collection: The GSK Experience

Zoe Blaxill, GSK

  • To Serve & Protect: Compound Management for Discovery Research

John Morin, Wyeth

  • Libraries for Fragment Screening

Ijen Chen, Vernalis

  • Building a high quality screening library from commercial sources

Justin Bryans, MRCT

  • Application of Chemogenomics to Compound Design

Steve Garland, GSK

The Hard Cell: Current issues in Drug Discovery and Screening

Session Chairs: Richard Eglen, Perkin Elmer and Martin Coldwell, AstraZeneca

  • Experiences of the Application of Label-Free Technologies for compound profiling in cell- base assays

Kathy Dodgson, AstraZeneca

  • Cell Based Screening for GPCR Ligands; Strategies, Successes and Future Challenges

Steve Rees, GSK

  • Title to be confirmed

Stefan Precti, Bayer

  • Screening Biologics in Cell Based Assays

Paula Harrison, Medlmmure

  • Ion channel targets and HTS: a comprehensive platform of luminescent and fluorescent cellular-based assays

Viviana Agus, Axxam

  • Development of KinobeadsTM assays for lead optimisation

Dan Leggate, Cellzome

Wednesday, 24 September

Liquid Handling and Detection Technologies

Session Chairs: Graeme Daniels, Tecan, Eric Tang, AZ and John Comley, HTStec

  • FDSS7000, a novel 1536 well multi-readout cellular assay platform for kinetic assays

Rochdi Bouhelal, Novartis

  • HTS operations: How to choose the right components?

Sabrinna Corazza, Axxam

  • Leveraging Hybrid Microplate Detection to Optimize Enabling Assay Technologies for Cell Signaling and Membrane Targets

Kevin Lowitz, Invitrogen

  • Title to be confirmed

Eric Tang, AstraZeneca

  • Title to be confirmed

Florian Hollfelder, Cambs Uni

Biopharmaceutical Drug Discovery

Session Chairs: Sandra Turconi, Ablynx and Richard Pither, UCB

  • The Application of SPR and Kinetic Screening to Antibody selection

Robert Karlsson, GE Healthcare

  • Antibodies as Therapeutics and Tools in Drug Discovery

Alastair Lawson, UCB

  • Overcoming Adverse Immunogenicity Against Therapeutic Antibodies

Matthew Baker, Antitope

  • High density screening of domain antibodies

Rosemary Sasse, GSK

  • Monoclonal Antibody Generation with LIMS and Automation integration

Trevor Wattam, GSK

  • Nanoclone®: A novel high-throughput technology for isolating heavy chain antibody variable domains from single B-cells

Joost Kolkman, Ablynx

Drug Discovery for GPCR targets

Session Chairs: Stephen Hill, Nottingham University and Fiona Marshall, Heptares

  • New Tools for Studying GPCR Targets

Annette Gilchrist, Caden Bio

  • Engineering stabilised GPCRs in agonist and antagonist conformations

Fiona Marshall, Heptares Therapeutic

  • Structure based design of adenosine receptor antagonists

Stefano Moro, Uni of Padova

  • Structure of the Beta Adrenergic Receptors: Progress in obtaining recombinant G protein Coupled Receptor Structure

Gebhard Schertler, Cambridge

  • Label-free technology fulfilling the potential for GPCR drug discovery

Martyn Wood, GSK

  • Development of Allosteric Modulators of GPCSs as a Novel Approach for the Treatment of CNS Disorders

Carrie Jones, Vanderbilt Uni

Useful Websites

www.elrig.org

www.sbsonline.org