Our ability to rationally develop new drugs or engineer proteins is limited by an inadequate understanding of conformational dynamics of biomolecules. We have previously established that proteins sample a restricted, yet functionally relevant, conformational ensemble in a crystalline environment. Unfortunately, the ensembles present themselves as unresolved, spatiotemporally averaged data in X-ray diffraction experiments. Our work has centered on overcoming this limitation by resolving ensembles with multi-temperature X-ray crystallography and multi-conformer models Our central hypothesis is that today's structural models disproportionately target the ensemble average, masking important functional and allosteric molecular mechanisms. The objective of this research program is to use multi-temperature X-ray crystallography and multi-conformer models to access multi-scale heterogeneity and shifting equilibria of proteins and protein- ligand systems. We will pursue the following specific aims: 1. Map the conformational landscapes of PTP1B and AR by Multitemperature Multiconformer X-ray crystallography (MMX). To examine functionally important loop regions, we will create and validate new automated procedures for our qFit algorithm to accurately model large backbone heterogeneity. We will apply MMX to PTP1B, a validated diabetes target, and Androgen Receptor (AR), an important prostate cancer target with new emerging drug resistance. 2. Exploit MMX models for allosteric ligand discovery in PTP1B and Androgen Receptor. We have already identified novel allosteric modulators for the diabetes therapeutic target protein tyrosine phosphatase 1B (PTP1B) by multitemperature crystallography and ligand tethering. We will determine structures and test novel ligands of AR resistance mutants. 3. Map conformational coupling at protein-ligand binding interfaces by MMX. We will create and validate new procedures for our qFit algorithm to model ligand conformational distributions and solvated amino acids, which is important for ligand optimization. We will perform large-scale validation tests of our algorithms. Our research program will have a positive impact by enabling discovery-driven, translational ligand optimization. Robust experimental and computational methods to access conformational ensembles, in a manner complimentary to NMR and molecular dynamics, that would open up a new and exciting and avenue to reveal molecular mechanisms not only from conventional synchrotron data, but also from time-resolved experiments at new XFEL lightsources and from cryoEM.

Public Health Relevance

This proposal describes new methods for identifying the structural basis of conformational dynamics in macromolecules. Knowledge of how protein and ligands can adopt multiple conformations will greatly aid structure-based drug design, which is an important paradigm for developing new chemical entities interrogating biology and for treating disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM123159-02S1
Application #
9868837
Study Section
Program Officer
Smith, Ward
Project Start
2019-01-01
Project End
2019-12-31
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Keedy, Daniel A; Hill, Zachary B; Biel, Justin T et al. (2018) An expanded allosteric network in PTP1B by multitemperature crystallography, fragment screening, and covalent tethering. Elife 7:
Budday, Dominik; Leyendecker, Sigrid; van den Bedem, Henry (2018) Kinematic Flexibility Analysis: Hydrogen Bonding Patterns Impart a Spatial Hierarchy of Protein Motion. J Chem Inf Model 58:2108-2122
Otten, Renee; Liu, Lin; Kenner, Lillian R et al. (2018) Rescue of conformational dynamics in enzyme catalysis by directed evolution. Nat Commun 9:1314
Wall, Michael E; Wolff, Alexander M; Fraser, James S (2018) Bringing diffuse X-ray scattering into focus. Curr Opin Struct Biol 50:109-116