This study will examine the specialized molecular features of the integrin ?v8 that enables activation of latent-TGF-. The activation of latent-TGF- is a critical step in the initiation of fibroinflammatory processes that occur during airway disease and other fibrotic lung diseases. There are dual long-term goals of this study. The first is to understand the structural mechanism by which integrins modulate their ligand-binding properties and the second is to acquire a deep understanding of the process of TGF- activation to develop new strategies and treatments for airway disease in COPD.
Three AIMs address this goal using new technological developments in electron microscopy to study the structure of difficult to study proteins: 1) Single particle electron cryomicroscopy to determine the near atomic structure of an integrin ectodomain in the extended fully active conformation, something that has not been achieved before. We focus on the integrin ?v8 an integrin unusual in its conformational homogeneity and propensity to extend. 2) Single particle electron cryomicroscopy to determine the near atomic structure of the integrin ?v8 in complex with latent-TGF-. The complex of an integrin with latent-TGF- has not yet been solved, which is an essential step in mechanistic understanding of latent-TGF- activation, and rational design and optimization of inhibitors. 3) Single particle electron cryomicroscopy to understand the mechanistic basis of integrin allosteric regulation of ligand-binding affinity. We will use allosteric blocking and non-blocking Fab fragments to address the conformational changes associated with integrin ?v8 ligand-binding affinity. These studies will address the key question in lung fibrosis biology: What are the basic structural mechanisms underlying the initiation of signals that cause and sustain inflammation and the fibrotic responses? The successful completion of these AIMs will be transformative in integrin structural biology and allow the first atomic-level understanding of the mechanistic basis of integrin allostery in an intact integrin. We will understand the mechanistic basis of antibody inhibitors that show efficacy in preclinical models to treat airway remodeling. Structures obtained will simultaneously reveal new insights into the structural basis of integrin function, while providing the mechanisms of action of allosteric integrin inhibitors.

Public Health Relevance

The multifunctional cytokine transforming growth factor- (TGF-), which is activated by integrins, is at the apex of a series of pathologic events culminating in fibroinflammatory lung disease. This project aims to understand the structural basis of integrin-mediated TGF-? activation with the goal of accelerating the conception and design of new methods to regulate the TGF-? activation mechanism.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL134183-04
Application #
9685933
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Craig, Matt
Project Start
2016-07-04
Project End
2021-04-30
Budget Start
2019-05-01
Budget End
2021-04-30
Support Year
4
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pathology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Cormier, Anthony; Campbell, Melody G; Ito, Saburo et al. (2018) Cryo-EM structure of the ?v?8 integrin reveals a mechanism for stabilizing integrin extension. Nat Struct Mol Biol 25:698-704
Takasaka, Naoki; Seed, Robert I; Cormier, Anthony et al. (2018) Integrin ?v?8-expressing tumor cells evade host immunity by regulating TGF-? activation in immune cells. JCI Insight 3:
Cheng, Yifan (2018) Single-particle cryo-EM-How did it get here and where will it go. Science 361:876-880
Cheng, Yifan (2018) Membrane protein structural biology in the era of single particle cryo-EM. Curr Opin Struct Biol 52:58-63
Palovcak, Eugene; Wang, Feng; Zheng, Shawn Q et al. (2018) A simple and robust procedure for preparing graphene-oxide cryo-EM grids. J Struct Biol 204:80-84