Cambridge Healthtech Institute 제3회

GPCRs & Membrane Proteins
(GPCR과 막단백질)

복수의 막관통 도메인을 가진 단백질을 표적으로 한 약제의 설계

2019년 4월 10일-11일

 

G단백질 연결 수용체(GPCR) 등의 세포표면 복합막단백질 및 이온채널, 수송체는 의약품의 설계와 Drug Discovery의 매력적인 표적입니다. 이것은 생리학적으로 중요한 역할을 담당하고 있으며 체내를 순환하는 신약이 될 가능성이 있는 화합물에도 접근할 수 있으나, 모두 막에 묻혀 있다는 성질을 가지고 있으므로 단백질의 가용화에 의존하여 X선 결정 구조를 얻는 구조 기반 의약품 설계법에서는 다루기 어렵다는 문제가 있습니다. 그러나 가용화를 촉진하는 유전자 기술, 막과 결합한 상태로 단백질 연구를 가능하게 하는 우수한 생물물리학적 툴, 전자현미경의 진보보다 복합막단백질에 대응하는 합리적인 약제의 설계와 스크리닝이 가속하고 있습니다. GPCR과 막단백질을 테마로 한 이 컨퍼런스 프로그램에서는 의약화학, 구조생물학, 생물물리화학, 중개연구에 참여하고 있는 연구자가 한자리에 모여 GPCR 등의 복합막단백질에 관한 새로운 정보 및 연구를 위한 툴이 표적 기반 약제의 설계에 미치는 영향에 대해 논의합니다.


Final Agenda

Wednesday, April 10

12:30 pm Registration Open

12:45 Dessert Break in the Exhibit Hall with Poster Viewing

막단백질의 구조 연구 진전

1:30 Welcome Remarks

Anjani Shah, PhD, Senior Conference Director, Cambridge Healthtech Institute

1:35 Chairperson’s Opening Remarks

Irina Kufareva, PhD, Associate Adjunct Professor, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego

1:40 Structure-Based Ligand Discovery for Class 'A' GPCRs: New Targets and Approaches

Vsevolod 'Seva' Katritch, PhD, Assistant Professor, The Bridge Institute, University of Southern California

With the rapid accumulation of high-resolution crystallographic and cryo-EM data for GPCRs, structure-based virtual ligand screening and rational design are quickly finding their prominent place as mainstream lead discovery and optimization tools. This talk will discuss several recently emerged structural targets for pain, addiction and immune disorders, as well as updates in virtual screening approaches we use to discover new chemotypes as probe compounds for these targets.

2:10 Nanobody-Stabilized Kappa Opioid Receptor Structure and Implications for Biased Opioid Ligand Design

Tao Che, PhD, Postdoctoral Fellow, Bryan Roth Lab, Department of Pharmacology, University of North Carolina Chapel Hill

This presentation will cover the design of biased ligands at the kappa-opoioid receptor (KOR) using the crystal structure of KOR as a model.

2:40 CXC Chemokine Receptor 4: Structural Updates on a Druggable Target

Irina Kufareva, PhD, Associate Adjunct Professor, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego

As a key driver of cancer cell migration and metastasis, the CXC chemokine receptor 4 is a target of several drug development programs. CXCR4 shares an endogenous chemokine CXCL12 with the atypical, intrinsically biased receptor ACKR3, but the structural principles of chemokine binding and receptor activation remain unknown. Our work reveals the basis for CXCL12 interaction and activation of CXCR4, and comparison with ACKR3, with potential implications for drug design.

3:10 Sponsored Presentation (Opportunity Available)

3:40 Refreshment Break in the Exhibit Hall with Poster Viewing

4:30 Crystal Structure of the Frizzled 4 Receptor in a Ligand-Free State

Fei Xu, PhD, Assistant Professor, iHuman Institute, Shanghai Tech University

We present the first atomic-resolution structure of the human Frizzled 4 receptor (FZD4) transmembrane domain (TMD) in the absence of a bound ligand. The structure reveals an unusual transmembrane architecture distinct from all other GPCR structures reported to date. Within this unique transmembrane fold is an extremely narrow and highly hydrophilic pocket that is not desirable for traditional GPCR ligand design.

5:00 First-in-Class Small Molecule Modulators of Adhesion GPCRs

Gregory Tall, PhD, Associate Professor, Pharmacology, University of Michigan

Adhesion GPCRs control many aspects of developmental transitions, tissue maintenance in adults, and a slew of regulatory functions in various tissues. There is a paucity of small molecule ligands to manipulate the receptor subclass. We recently demonstrated that adhesion GPCRs are activated by a tethered-peptide-agonist mechanism. With this understanding, we engineered receptors for high throughput screening of chemical libraries. We found the first adhesion GPCR small molecule antagonist and the first small molecule partial agonist.

5:30 Breakout Discussions - View All Breakouts

In these sessions, attendees choose a specific roundtable discussion to join. Each group has a moderator to ensure focused conversations around key issues within the topic. The small group format allows participants to informally meet potential collaborators, share examples from their work and discuss ideas with peers.

Topic: New Ways to Screen GPCRs

Moderator to be Announced

  • Physiologically relevant cells and assays
  • High-content screening
  • Screening for biased ligands

Topic: Opioid Alternatives and GPCRs

Moderator: Susruta Majumdar, PhD, Associate Professor of Pharmacology, Center for Clinical Pharmacology, St. Louis College of Pharmacy/Washington University

  • Impact of new structural GPCR insights on drug design for pain indications
  • Which biased ligands for opioid receptors are showing the most promise?
  • Best ways to find opioid alternatives

Topic: New Drug Discovery-Related Technologies for Complex Membrane Proteins

Moderator: Matthew Eddy, PhD, Assistant Professor, Chemistry, University of Florida

  • XFEL and other crystallography advances
  • NMR applications for drug screening
  • cryoEM: current applications and future directions

6:15 Close of Day

6:30 Dinner Short Courses*

*Premium or separate registration required.

Thursday, April 11

8:00 am Breakfast Presentation (Sponsorship Opportunity Available) or Morning Coffee


8:45 Welcome Remarks from Lead Conference Director

Anjani Shah, PhD, Senior Conference Director, Cambridge Healthtech Institute

8:50 Plenary Keynote Introduction

8:55 Plenary Keynote: New Ways of Targeting K-Ras

Frank McCormick, PhD, Professor, HDF Comprehensive Cancer Center, University of California San Francisco

Efforts to find drugs that bind K-Ras directly have increased recently, enabled by NMR-based fragment screening, di-sulfide tethering, in silico drug design and biophysical methods such as Second Harmonic Generation (SHG). We will report progress on attacking two sites in the K-Ras protein; cysteine-185 (the site of prenylation), and histidine-95, a residue unique to K-Ras, to develop covalent K-Ras inhibitors, as well as compounds identified by SHG and other methods.

9:45 Coffee Break in the Exhibit Hall with Poster Viewing

트랜스포터와 이온채널

10:40 Chairperson’s Remarks

Matthew Eddy, PhD, Assistant Professor, Chemistry, University of Florida

10:45 A New Era in Discovery of Solute Carrier (SLC) Transporter Modulators

Alan D. Wickenden, PhD, Scientific Director, Discovery Sciences, Janssen R&D

SLC transporters constitute the second largest family of membrane proteins in the human genome and a rich and relatively untapped source of therapeutic drug targets. Unfortunately, the identification of new SLC modulators has been limited. This talk will review recent progress in understanding the structural and molecular basis of SLC transporter function and describe the opportunities these new insights may present for SLC transporter drug discovery.

11:15 Discovery of GLPG2451, a Novel Potentiator for the Treatment of Cystic Fibrosis

Steven Van der Plas, PhD, Group Leader, Medicinal Chemistry, Galapagos

Cystic Fibrosis is caused by mutations in the Cystic Fibrosis Transmembrane Regulator (CFTR) gene, resulting in loss of fuction of the CFTR ion channel. Potentiators are a class of CFTR modulators that allow the effective opening of the CFTR channel by increasing its open probability. I describe the discovery and optimisation of a novel series of potentiators. Additionally, the clinical compound GLPG2451 will be disclosed and its properties will be discussed.

11:45 Sponsored Presentation (Opportunity Available)

12:00 pm Presentation to be Announced

12:30 Luncheon Presentation: Stabilization of Native Membrane Protein Targets for Drug Discovery

Anass Jawhari, PhD, CSO, CALIXAR

CALIXAR has developed an innovative detergent/surfactant-based approach for therapeutic membrane protein stabilization. GPCRs, ion channels, transporters can be stabilized without any single mutation, truncation or fusion. We will illustrate that using most recent case studies on targets of high medical relevance for which functional and structural integrities were preserved. This innovative approach represents a serious alternative to classical protein engineering approaches to enable drug discovery (SBDD, FBDD, Antibody Discovery & Vaccine).

1:30 Dessert Break in the Exhibit Hall with Poster Awards Announced

Poster Awards Sponsored by Domainex

화학 연구자의 GPCR 약리학, 약물 동태, 신호 전달 관련 문제

2:15 Chairperson’s Remarks

Dean G. Brown, PhD, Director, External Chemistry, Hit Discovery, Discovery Sciences, IMED Biotech Unit, AstraZeneca

2:20 FEATURED PRESENTATION: One Receptor, Many Partners: How do GPCRs Stimulate Diverse Signaling Proteins?

Ron O. Dror, PhD, Associate Professor, Computer Science, Stanford University

The search for functionally selective or biased ligands that promote GPCR signaling through desired but not undesired pathways represents a major current focus of drug discovery efforts. To enable the rational design of such biased ligands, we are using atomic-level simulations, together with complementary experimental data, to determine how GPCRs cause various intracellular proteins—including arrestins, kinases, and G proteins—to activate and signal.

2:50 The Good, the Bad, and the Confusing: Binding Kinetics at GPCR Targets and Potential Effects on Lead Optimization and Translatability

Brian Murphy, PhD, Senior Principal Scientist, CV and Fibrosis Drug Discovery, Disease Sciences and Biologics, R&D, Bristol-Myers Squibb

Small molecule binding kinetics likely plays an important role in determining both in vitro potency and in vivo efficacy of compounds. For example, compound off-rate may affect the duration of action of compounds in vivo. I will review literature data in support of, and in contradiction to the notion that residence time is a critical factor in compound efficacy in vivo. I will also show examples where in vitro measures of compound affinity and efficacy can be compromised without consideration of compound binding kinetics.

3:20 FEATURED PRESENTATION: GPCRs as Allosteric Sensors Linking Hormone Binding to G Protein Activation to Modulation by Small Molecules and Cations


Roger K. Sunahara, PhD, Professor, Pharmacology, University of California San Diego

G protein-coupled receptors (GPCR) are critical conduits that sense and communicate extracellular stimuli. Their diversity and physiological importance thus make them superb therapeutic targets. Recent advances in the structural biology of GPCRs, along with support from pharmacological and biochemical studies, has helped in understanding the mechanism of GPCR activation and also has been informative for structure-based drug design. We will discuss our recent data on receptor allostery and structure-based drug design of subtype-specific GPCR ligands.


3:50 Networking Refreshment Break

통증 및 중추신경계의 표적화:대체 오피오이드 및 각종 진통제

4:20 Chemistry and Pharmacology of Mitragyna Speciosa

Susruta Majumdar, PhD, Associate Professor of Pharmacology, Center for Clinical Pharmacology, St. Louis College of Pharmacy/Washington University

Mitragyna Speciosa, also known as Kratom, originates from the leaves of a tropical tree found in South-East Asia. It has been shown to have pain-relieving properties with less withdrawal effects compared to other opioids. I will discuss the chemistry and pharmacology of Mitragyna Speciosa and present evidence for the biased agonism of the compound.

4:50 Development of D3 Dopamine Receptor Selective Bitropic Ligands

Robert Luedtke, PhD, Professor, Department of Pharmacology and Neuroscience, University of North Texas Health Science Center

I will focus on the development of bitropic D3 dopamine receptor selective ligands for the treatment of cocaine abuse. Though D2 and D3 dopamine receptors have a high level of amino acid sequence homology, we have been able to identify compounds with high binding affinity at the D3 dopamine receptor subtype and that possess greater than 100 fold degree of D3 vs. D2 receptor binding selectivity. Our dopamine GPCR subtype selective ligands resulted from collaborations between medicinal chemists, computational chemists and behavioral pharmacologists.

5:20 Structure, Dynamics and Activation of the CGRP Receptor, a Medically Important Class B GPCR

Christopher Reynolds, PhD, Professor, Royal Society Industry Fellow, School of Biological Sciences, University of Essex

Calcitonin gene-related peptide (CGRP) is a widely expressed neuropeptide; antagonists can be used to treat migraine while agonists are cardioprotective. The CGRP receptor is a heterodimer of the calcitonin receptor-like receptor (CLR) class B G-protein-coupled receptor and the type 1 transmembrane domain protein, receptor activity modifying protein (RAMP) 1. I will present dynamics and activation of the CGRP receptor in complex with the CGRP peptide and the Gs-protein heterotrimer based on our recent 3.3 Å cryo-electron microscopy structure of the human CGRP receptor, photoaffinity labelling studies, and molecular dynamics simulations. Our results also provide novel insights into the role of RAMPs in the activation of the CGRP receptor.

5:50 Close of Conference

* 주최측 사정에 따라 사전 예고없이 프로그램이 변경될 수 있습니다.