G-protein coupled receptors (GPCRs) play roles in many physiological processes and have therefore been the target of medical therapeutics for decades. Their complexities in signaling, however, are still being unraveled and starting to be exploited for
more targeted therapies. For example, therapeutics with fewer side effects are being sought by finding biased ligands of specific GPCRs that will activate or block the pathway of medical interest while not initiating less desirable signaling cascades
that the GPCR also controls. Progress in biophysical techniques and cryo-electron microscopy have also aided targeted drug discovery against GPCRs by enabling biosensor-based screens or by helping elucidate structural features of GPCRs that guide
structure-based drug design. At CHI’s well-established GPCR-Based Drug Discovery conference, join colleagues and experts in the GPCR field who hail from both academics and industry to review advances in the field and discuss cutting edge topics
impacting drug development against this very medically relevant class of drug targets.
RECOMMENDED PREMIUM PACKAGE:
Choose 2 Short Courses and 2 Conferences/Training Seminars
September 16 Pre-Conference Short Course: SC1: Immunology Basics: Focusing on Autoimmunity and Cancer
September 17-18 Training Seminar: TS1: Targeting GPCRs for Drug Discovery
September 18 Dinner Short Course: SC8: GPCR Structure-Based Drug Discovery
September 18-19 Conference: GPCR-Based Drug Discovery
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Wednesday, September 18
10:50 - 11:50 BRIDGING LUNCHEON PANEL DISCUSSION: GPCRs: Leveraging Years of Data for Transformative Drug Discovery
This 1-hour panel
moderated by Michel Bouvier, PhD, Principal Investigator & CEO, Institute for Research in Immunology and Cancer (IRIC) and Professor, Department of Biochemistry and Molecular Medicine, Faculty of Medicine, Université de Montréal will feature two talks related to new horizons in GPCR drug discovery. The talks will be followed by a question and answer session.
-GPCR Mutations: Towards a More Personalized Drug Discovery
Olivier Lichtarge, MD, PhD, Molecular and Human Genetics, Computational and Integrative Biomedical Research Center, Baylor College of Medicine
-Virtual Screening: A Post-Structural Era
John Irwin, PhD, Adjunct Professor, Department of Pharmaceutical Chemistry, University of California, San Francisco
11:20 Conference Registration Open
11:50 Session Break
12:20 pm Event Chairperson’s Opening Remarks
An-Dinh Nguyen, Team Lead, Discovery on Target 2019, Cambridge Healthtech Institute
12:30 Plenary Keynote Introduction
Anjan Chakrabarti, Vice President, Discovery Chemistry, Syngene International Ltd
12:40 Base Editing: Chemistry on a Target Nucleotide in the Genome of Living Cells
David R. Liu, PhD, Howard Hughes Medical Institute Investigator, Professor of Chemistry & Chemical Biology, Harvard University
1:20 PROTACs: Past, Present, and Future
Craig M. Crews, PhD, Professor, Chemistry; Pharmacology; Molecular, Cellular & Developmental Biology; Yale University
2:00 Close of Plenary Keynote Program
2:00 Dessert Break in the Exhibit Hall with Poster Viewing (America Ballroom)
2:45 Organizer's Welcome Remarks
2:50 Chairperson’s Opening Remarks
Ajay Yekkirala, Co-Founder and CSO, Blue Therapeutics
2:55 Design and Preclinical Profile of a GPR40 Superagonist
Mark R. Player, MD, PhD,
Senior Scientific Director & Fellow, Discovery Chemistry, Janssen Pharmaceutical Research & Development
Full agonists of GPR40 exhibit superior glucose lowering to partial agonists in pre-clinical species due to increased insulin and GLP-1 secretion, the latter also promoting weight loss. We have identified a GPR40 superagonist which displayed excellent
in vitro potency and superior efficacy in the Gas-mediated signaling pathway. Design and preclinical efficacy (human islets, oGTT and weight loss in DIO mice) and safety data (DILI-derisking, pancreatic insulin/proinsulin
after compound rechallenge in Wistar rats) will be presented.
3:25 GLP1-R Agonist
David A. Griffith,
PhD, Research Fellow, Medicinal Chemistry, Pfizer Global R&D
Glucagon-like peptide-1 receptor (GLP-1R) agonists comprise a growing class of agents that deliver unprecedented efficacy in diabetes. We will report on a program to identifyan oral, small molecule GLP-1 receptor agonist
for the treatment of diabetes. An innovative hit identification strategy provided weak leads that were progressed through structure-activity exploration to achieve drug-like potency and ADMEattributes. This presentation will disclose
the discovery of the oral small molecule GLP-1R agonist PF-06882961, including emerging human pharmacokinetic data.
3:55 Enabling Drug Discovery with Multispan
Lisa Minor, Scientific Consultant, Multispan, Inc.
The path to successful drug discovery requires 1) a validated target, 2) assays accurately measuring the specific target, and 3) assays run reproducibly and robustly. This presentation will demonstrate how Multispan can uniquely empower your drug discovery
efforts. We provide fully validated cells expressing your target along with a battery of well characterized MultiScreen™ assays for conducting your primary and secondary screens in our Bay Area laboratory. Our vast attention to detail
and cellular pharmacology helps to ensure your project's success and shorten your timeline.
4:25 Refreshment Break in the Exhibit Hall with Poster Viewing
5:00 Signaling Bias of a Novel LPAR1 “Antagonist” Lead Molecule and Implications for Drug Discovery
Rives, PhD, Senior Scientist, Molecular and Cellular Pharmacology, Lead Discovery, Janssen Research & Development
Lysophosphatidic acid (LPA) is a bioactive lipid and pro-fibrotic agent acting through LPA receptors: LPAR1 - 6. A wealth of preclinical data has revealed the relevance of LPAR1 in the development of fibrotic diseases. We have identified a new LPAR1 allosteric
antagonist that shows promising selectivity. However, this compound and its analogs show intriguing signaling bias properties whose physiological consequences are still unknown and under investigation.
5:30 GPR84: Can Context-Dependent Signaling Inform Therapeutic Direction?
Carleton Sage, PhD, Vice
President, Computational Sciences, Beacon Discovery
GPR84 is an inflammation-related orphan G Protein-Coupled GPCR. Expression analysis suggests that modulation of GPR84 could be valuable for inflammation related diseases such as Crohn’s disease, IBD, or idopathic pulmonary fibrosis, but thus far
agonists have proven unsuccessful in clinical trials. New observations of signaling in immune cells suggest an explanation and a path forward.
6:00 Drug-Target Binding Kinetics – Implications for Insurmountable Antagonism at GPCRs
Laura H. Heitman,
PhD, Associate Professor for Molecular Pharmacology, Leiden Academic Centre for Drug Research (LACDR), Leiden University
The success rate of a candidate drug moving to the pre-clinical development phase is disappointingly low, mainly due to lack of clinical efficacy. Novel drug discovery concepts (e.g. target binding kinetics and allosteric modulation) might offer a different
mechanism of action for drug candidates. Specifically, today’s talk will show new avenues for CCR2, and GPCR small molecule drug discovery.
6:30 Dinner Short Course Registration (America Foyer)
Click here for details on short courses offered.
9:30 Close of Day
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Thursday, September 19
7:00 am Registration Open (America Foyer)
7:30 Interactive Breakfast Breakout Discussion Groups - View All Breakouts
Grab a cup of coffee and join a breakout discussion group. These are informal, moderated discussions with brainstorming and interactive problem solving, allowing participants from diverse backgrounds to exchange ideas and experiences and develop future
collaborations around a focused topic.
Moderator: John Janetzko, PhD, Damon Runyon Postdoctoral Fellow, Kobilka Lab, Department of Molecular and Cellular Pharmacology, Stanford University
- Structural determinants of ligand bias
- The role of GRKs in biased signaling
- Cryo-EM of GPCR complexes and its role in drug discovery
- How can academic research help the development of new drugs?
GPCR Targeted Lead-Development Challenges
Moderator: Phil Carpino, PhD, Scientific Director, Discovery Chemistry, Janssen Research & Development
- Untangling biased signaling
- Comparing various cell-based screens
- Medicinal chemistry challenges
GPCR-Ligand Binding Kinetics
Moderator: Sam Hoare, PhD, Founder, Pharmechanics LLC
- Compound residence time vs. compound in vivo efficacy
- Off rate and duration of action
- Kinetic artifacts in SAR assays
8:30 Transition to Sessions
8:40 Chairperson’s Remarks
Huixian Wu, PhD, Principal Scientist, Structural and Molecular Sciences, Discovery Sciences, Pfizer, Inc.
8:45 FEATURED PRESENTATION: Bias and Beyond: Challenges and Opportunities in GPCR Drug Development
Michael Fossler, PharmD, PhD, FCP, Vice President, Clinical Operations and Quantitative Sciences, Trevena, Inc.
Oliceridine is a novel investigational G protein-biased ligand at the µ-opioid receptor developed for the management of moderate to severe acute pain. Oliceridine produced differentiated pharmacology in preclinical studies compared to unbiased ligands
and maintained a similar profile in the clinic—rapid analgesia with a favorable safety profile with regard to respiratory and gastrointestinal adverse effects compared to morphine. The totality of the data indicate that ligand bias is an important
concept in designing new drugs.
9:15 De novo Design of Gα Mimetics: Generalizable Tools for Allosteric Control of G Protein-Coupled Receptors
Christopher D. Bahl, PhD, Head of Protein Design, Institute for Protein Innovation
Generalizable tools to stabilize the active conformational state of GPCRs will facilitate protein purification and structure determination, as well as accelerate the engineering of molecules which act as agonists or antagonists. Using de novo protein design, we have developed novel Galpha mimetic proteins that are thermostable, selectively bind to the active state of GPCRs, and can bind to a wide range of different GPCRs.
9:45 Structure-Based Conversion of the Subtype Selectivity of the Muscarinic Toxin
Shoji Maeda, PhD, Senior
Postdoctoral Fellow, Kobilka Lab, Department of Molecular and Cellular Physiology, Stanford University
Muscarinic toxin 7 (MT7) is a natural protein toxin produced by green mamba snakes that exclusively binds to muscarinic acetylcholine receptor 1 (M1R) and modulates its function. To understand the molecular mechanism of this strict subtype selectivity
and allosteric mechanism, we solved the crystal structure of M1R-MT7 complex. Furthermore, we converted the selectivity of MT7 towards M2R by in vitro engineering. This study suggests the possibility of the three-finger fold as a promising scaffold
to target GPCRs.
10:15 Coffee Break in the Exhibit Hall with Poster Viewing and Poster Competition Winner Announced (America Ballroom)
10:55 Understanding the Consequences of GPCR Dimerization
PhD, Professor, Department of Pharmacology and Therapeutics, McGill University
How GPCRs interact with one another remains an area of active investigation. Well-characterized dimers of class C GPCRs such as GABA-B and glutamate receptors are well accepted, but whether this is a general feature of GPCRs is still debated. GPCR oligomers
are better imagined as parts of larger metastable signaling complexes. The nature of functional oligomeric entities, stability, kinetic features and structural and functional asymmetries of such metastable entities have implications for drug discovery.
11:25 NEW: Breakout Discussions Report-Back
11:55 Using Smart Drug Discovery Software to Enhance Collaboration and Manage Disperse Assay Data
Robert Thorn, PhD, Customer Engagement Scientist, Collaborative Drug Discovery, Inc.
12:10 pm Machine-Learning & AI-Based Approaches for GPCR Bioactive Ligand Discovery
Raschka, PhD, Assistant Professor, Department of Statistics, University of Wisconsin at Madison
This talk will provide an overview of the latest advances for automating the discovery of bioactive ligands using machine learning. Applications include the discovery of a potent GPCR pheromone inhibitor as well as models predicting active and inactive
GPCR states by combining machine learning and structural rigidity analysis. Lastly, the talk will conclude with the recent developments in deep learning that are aimed at replacing the need for hand-engineering molecular representations by automatic
12:40 Session Break
12:45 Luncheon Presentation: Integrating Experimental and Computational Pharmacology for Intelligent GPCR Drug Candidate Selection
Martin Ostermaier, PhD, CEO, InterAx Biotech AG
InterAx built a computational tool to integrate theoretical knowledge with experimental data of GPCR-mediated trafficking events. As a result, deeper mechanistic insights into the dynamic cellular system are achievable. Such mathematical models allow
to predict experimental outcomes and deliver novel insights into drug actions on GPCRs. As an example, our predictive model allowed us to discriminate 17 marketed asthma drugs for their duration of action. This technology is currently applicable
to discovery programs on GPCRs.
1:25 Refreshment Break in the Exhibit Hall with Poster Viewing
2:05 Chairperson’s Remarks
Mark R. Player, MD, PhD, Senior Scientific Director & Fellow, Discovery Chemistry, Janssen Pharmaceutical Research & Development
2:10 Lessons Learned from Various GPCR Lead Optimization Projects
Chi Sum, PhD, Senior Research Investigator, Lead Discovery and Optimization, Bristol Myers Squibb & Co.
The recent new concepts of GPCR function, including signaling bias, allosteric, kinetics, and receptor trafficking, have provided an important frame of reference for GPCR Drug Discovery. Recognizing these pharmacological properties has become
fundamental for a successful campaign. Here, we present some case studies on how these principles operate directly or indirectly to influence lead optimization effort.
2:40 First Orally Bioavailable Antagonist of the Neuropeptide Y Receptor 2 (NPY2R)
Wasnaire, PhD, Senior Scientist, Pharmaceuticals R&D, Bayer AG
Autonomic imbalance with increased sympathetic activity and withdrawal of vagal activity is associated with increased mortality both after myocardial infarction (MI) and in heart failure (HF). Neuropeptide Y (NPY) is suggested to be a key link
between enhanced sympathetic and decreased vagal activity in autonomic imbalance in HF. NPY receptor 2 (NPY2R) antagonism seems attractive for the treatment of autonomic imbalance by restoring vagal activity in HF patients and patients post-MI.
After high-throughput screening and medicinal chemistry optimization we found new, potent and selective NPY2R antagonist, showing suitable DMPK and safety profiles.
3:10 Structural Insights into GPCR Recognition by Arrestin
John Janetzko, PhD, Damon Runyon Postdoctoral Fellow, Kobilka Lab, Department of Molecular and Cellular Pharmacology, Stanford University
While there is a wealth of structural information pertaining to the basis of G protein-receptor interactions, there exists no structure of a non-rhodopsin GPCR in complex with arrestin. Using cryo-electron microscopy we obtained a structure of
the neurotensin type I receptor (NTSR1) in complex with arrestin 2. This structure reveals how the receptor is engaged by arrestin, how phosphorylation of the receptor might regulate arrestin recruitment and activation and how the plasticity
of the interactions formed between the two enable arrestin to recognize a large set of diverse GPCRs.
3:40 Surface Plasmon Resonance Microscopy for GPCRs
Shijie Wu, PhD, Application Scientist, Biosensing Instrument
One of the most recent significant biophysical advances to study GPCR binding properties is Surface Plasmon Resonance Microscopy (SPRM), a powerful technique that simultaneously visualizes cellular structures and measures molecular binding interactions
of membrane proteins label-free, in vitro and in real time. With this award-winning biosensor technique, the measurement of phenotypical changes of the cell via bright field and binding affinity and kinetics
of GPCR targets via SPR can be done. In this presentation, we will review the principles behind SPRM and show application examples of binding affinity and kinetics of multiple whole cells as well as localized responses on a single cell.
3:55 Close of Conference
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