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Home > Ion Channel Retreat 2008

6th Annual Ion Channel Retreat
write us at retreat@aurorabiomed.com

Read the Retreat Review

Vancouver BC, Canada • June 23 - 25, 2008
Marriott Vancouver Pinnacle Downtown

Aurora Biomed invites you to attend the 6th Annual Ion Channel Retreat. Our goal is to create a forum for scientific discourse spanning the spectrum of ion channel disciplines. Researchers from both academia and industry are invited to share knowledge for the advancement of ion channel research, ion channel technology, drug discovery and safety pharmacology.

Program Sessions:
• Ion Channel Screening Technologies
• Ion Channels in Safety Pharmacology
• Ion Channels as Disease Targets
• Ion Channels as Pain Targets
• Mechanisms of Ion Channel Signalling

2008 Scientific Advisory Board:

Min Li
Johns Hopkin School of Medicine
Professor, Dept. of Neuroscience & High Throughput Biology Center

Qiang Lu
Executive Director
Safety Pharmacology and Discovery Biology
WuXi PharmaTech Inc

Juergen Reinhardt
Novartis Institutes for Biomedical Research
Research Investigator II, Center for Proteomic Chemistry/Lead Finding Platform

Terry Snutch
Neuromed Technologies
Chief Scientific Officer

Jean-Pierre Valentin
AstraZeneca
Director, Safety Pharmacology, Safety Assessment UK

Presentations:

Arthur "Buzz" Brown (Chantest)
Alexei Bagrov (National Institute on Aging, NIH)
Xueying Cao (Novartis Institutes for BioMedical Research, Inc.)
Jeff Clare (Ion Channel Group, Millipore)
Sikander Gill (Aurora Biomed Inc)
Ralk Kettenhofen
(Axiogenesis AG)
Torben Neelands
(Abbott Laboratories)
Steve Smith
(Chantest)
Jerrel Yakel (NIH/NIEHS)

Program:

June 23 Monday
Ion Channels as Pain Targets
8:35 Chairman's remarks
8:40

Torben Neelands
Abbott Laboratories
Apparent Voltage-Dependence of A-425619, a Competitive TRPV1 Antagonist, is Due to Voltage-Dependent Capsaicin Potency at Human TRPV1 Receptors

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9:10 Aaron Gerlach
Icagen
KCNQ Channels:  Drug Discovery Targets for the Treatment of Epilepsy and Pain
9:40 Jeff Clare
Director, R&D
Ion Channel Group, Millipore
Targeting voltage-gated sodium channels for pain therapy

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10:10 Zhiyuan Li
Investigator and Head of Ion Channels Research Laboratory
Guangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences
Discovery of M2 Antagonists for New Antiviral drugs
10:40 Break
Ion Channels as Disease Targets
11:05 Chairman's remarks
11:10 Yi-Xin Qian
Amgen
Discovery of kv1.3 blockers for autoimmune diseases
11:40 Steve Goldstein
University of Chicago
Professor, Pediatrics, Physiology, Neurobiology and Molecular Medicine
Founding Director, Institute of Molecular Pediatric Sciences
Co-Director, Institute for Translational Medicine
University of Chicago, Pritzker School of Medicine
Improving on nature: designer toxins from animal venom scaffold expression libraries
12:10 Lunch
1:30 Alexei Bagrov
National Institute on Aging, NIH
Digitalis-like cardiotonic steroids; clinical and therapeutic applications

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2:00 Elizabeth Tringham
Neuromed Technologies
T-type channel blockers as a novel antiepileptic therapy
2:30 Jesus "Tito" Gonzales
Sr. Director, Ion Transport
Vertex Pharmaceuticals
CFTR Modulators for Treating Cystic Fibrosis
3:00 Gary Desir
Yale University
Kv1.3 and Synaptotagmin-7 Regulates Calcium-Dependent GUT4 traffic
3:30 Break
3:45 Gail Robertson
Associate Professor, Department of Physiology
University of Wisconsin
Physiology and Pharmacology of hERG 1a/1b Channels:  Implications for Inherited and Acquired Long QT Syndrome
Ion Channel Screening Technologies
4:15 Chairpersons remarks
4:20 Dr. Steve Smith
Chantest
Reading the ion channel library with QPatch-HT
4:50 Howard Zhang
Wyeth Research
NeuroScience Discovery
Validation of Quattro IonWorks Assays for Screening of State-Dependent Nav1.7 Blockers
 
June 24 Tuesday
Ion Channel Screening Technologies
8:30 Chairpersons remarks
8:35

Xueying Cao
Preclinical Safety Profiling/LFP, US
Novartis Institutes for BioMedical
Research, Inc.
Optimization of the QPatch Assay for "High Throughput" hERG Inhibition

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9:05 Steve Hess
Research Fellow
Invitrogen
Building Robust Ion Channel Assays for Lead Discovery and Safety Liability Assessment
9:35 Sikander Gill
Director of Assay Development
Aurora Biomed
Development of Screening Technology Using Synthetic Lipid Vesicles and ICR
10:05 Cristian Ionescu-Zanetti
Chief Scientific Officer
Fluxion
Enabling “Plate Reader” Simplicity in High Throughput Electrophysiology through Well Plate Integration with Microfluidics
10:35 Kun Lui
Wyeth Research
Cardiovascular and Metabolic Diseases
Voltage gated K+ channel blockers: from assay development to lead identification
11:05 Lazslo Kiss
Senior Research Fellow
Merck Research Laboratories
High Throughput Electrophysiology Screen of a 200K Library to Identify Delayed Rectifier Potassium Channel Inhibitors
11:35 Lunch
Ion Channels in Safety Screening
12:45 Chairpersons Remarks
12:50 Jean-Pierre Valentin
Director, Safety Pharmacology, Safety Assessment UK
AstraZeneca
Adverse Drug Reactions Link To Ion Channels Dysfunction
1:20 Fraser Moss
Postdoctoral Fellow
Div. Biology, California Institute of Technology
hERG K+ Channel Drug Block Underlying Acquired Long-QT Syndrome Probed With Natural And Unnatural Amino Acid Mutagenesis In Mammalian Cells
1:50 Arthur "Buzz" Brown
Chairman and CEO
Chantest
Channel Panel for Safety and Discovery Profiling

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2:20 Ralf Kettenhofen
Scientist
Axiogenesis AG
ES-derived Cardiomyocytes: A New, Predictive Tool for Drug Development and Safety Pharmacology

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June 25 Wednesday
Structure and Function
8:30 Chairpersons remarks
8:35 Craig January
Professor of Medicine and Physiology
University of Wisconsin
Cellular Dynamics International, Inc.
A Constitutively Open hERG K+ Channel
9:20 Jerrel Yakel
Senior Investigator
NIH/NIEHS
Structural determinates for apolipoproteinE–derived peptide interaction with the a7 nicotinic acetylcholine receptor :structural transitions triggered by agonist binding that induce channel opening.

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9:50 Jianmin Cui
Associate Professor, Spencer T. Olin Endowment Department of Biomedical Engineering
Washington University of St. Louis
The Interaction between the Voltage-Sensor and Cytosolic Domains in BK channel Activation and Its Modulation by Mg2+
10:20 Break
10:50 Vladislav Zarayskiy
Boston University
ADAR-mediated RNA editing of Orai1 is a key to different selectivity of store-operated channels
11:20 Min Li
Professor, Dept. of Neuroscience & High Throughput Biology Center
Johns Hopkin School of Medicine
Chemical activation of voltage-gated potassium channels
11:50 John Adelman
Professor
Oregon Health and Science University
TBA
12:20 Lunch
1:30 Jun Chen
Neuroscience Research
Abbott Laboratories
Molecular determinants of species-specific activation or blockade of TRPA1 channels
2:00 Andreas Jeromin
Manager, Methods Development
Allen Institutes for Brain Science
Single-molecule tracking and total-internal reflectance microscopy to monitor the membrane dynamics and organization of Kv4.2
2:30 Kewei Wang
Peking University and ChemPartner
Structural Insights into Kv4 K+ Channel Modulation by Auxiliary KChIP Subunits
3:00

Dong Liang
CEO
Aurora Biomed Inc.
Closing Remarks

 

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