(30 lines) Entitled ?Cost Effective, Synergistic Macromolecular Structure Determination, Analysis & Simulation?, this proposal involves systems at the heart of biology: CCT Eukaryote Chaperonin, RNA Polymerase II, and the Ribosome, all of which our colleagues are studying experimentally. We will develop unbiased methods to solve structures with less data. Interested in how molecular machines move as they function, we map out their state-space using multi-scale hybrid methods. All our methods and curated data will be disseminated freely. This project is timely as these macromolecular machines carry out key cellular functions. The tools we develop for structure determination, analysis and simulation will aid others in advancing biomedicine. Michael Levitt, the Principal Investigator has a long career of independent scientific research that started in 1967 when he was one of the first to work in computational biology. His early work set up the conceptual, theoretical and computational framework for protein and DNA structure refinement, structure analysis and macromolecular simulations. He makes computer codes available and continues hands-on software development. He has been productive, scientifically rigorous and impactful for half a century. Particularly innovative is his work for the past five years leading to original methods to both solve biomedically significant structures and simulate functional motion. These areas are continued here by a PI committed to mentoring young scientists as well as engaging in sustained research-community service and public outreach. 1. Develop Novel Approaches to Determination and Refinement of Macromolecular Complexes. The first sub-area will deal with determining the identity of amino acid side chains. The second sub-area will involve a new approach to automatic structure determination requiring no manual intervention. Both methods will be adapted to cryo-EM electron density maps. 2. Develop Novel Approaches to Pathway Analysis of Structures. The first sub-area will deal with structure curation. Essential for ribosome work, it will be increasingly useful as structures accumulate for other macromolecular complexes. The second sub-area focuses on methods to find reaction pathways from multiple structures of such complexes. The third sub-area will test and develop new methods for structure morphing with few degrees of freedom. The forth sub-area will use Molten Zone molecular dynamics to study functional movement. 3. Determine the State-Space of Functional Motion in Chaperonin, RNA Pol II, and the Ribosome. We will identify key states, morph between these states to find reaction paths and run molecular dynamics. Studying these biomedically significant systems in collaboration with experimental colleagues will reveal fascinating details of biology in action. This work will elucidate the relationship between structure and function in large macromolecular machines, a keystone of modern biomedical science.

Public Health Relevance

(8 lines) Entitled ?Cost Effective, Synergistic Macromolecular Structure Determination, Analysis & Simulation?, this proposal studies three systems at the heart of all biology: CCT eukaryote Chaperonin, RNA Polymerase II, and the Ribosome, all studied experimentally by our colleagues. We will continue development of unbiased methods to solve structures with less information and higher throughput. Interested in how these machines move as they function, we approach the problem by mapping out conformational state-space using multi- scale hybrid methods. All methods we develop and data we curated will be disseminated freely. This project is timely as these macromolecular machines carry out key cellular functions. Our proven tools for structure determination, analysis and simulation will also help others advance biomedicine.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
5R35GM122543-03
Application #
9700473
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Lyster, Peter
Project Start
2017-06-01
Project End
2022-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Stanford University
Department
Biology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Ben-Aharon, Ziv; Levitt, Michael; Kalisman, Nir (2018) Automatic Inference of Sequence from Low-Resolution Crystallographic Data. Structure 26:1546-1554.e2
Scaiewicz, Andrea; Levitt, Michael (2018) Unique function words characterize genomic proteins. Proc Natl Acad Sci U S A 115:6703-6708
Li, Po-Nan; Herrmann, Jonathan; Tolar, Bradley B et al. (2018) Nutrient transport suggests an evolutionary basis for charged archaeal surface layer proteins. ISME J 12:2389-2402
Pataki, Camille I; Rodrigues, João; Zhang, Lichao et al. (2018) Proteomic analysis of monolayer-integrated proteins on lipid droplets identifies amphipathic interfacial ?-helical membrane anchors. Proc Natl Acad Sci U S A 115:E8172-E8180
Houdayer, Jérôme; Poitevin, Frédéric (2017) Reduction of small-angle scattering profiles to finite sets of structural invariants. Acta Crystallogr A Found Adv 73:317-332
Gruber, Ranit; Levitt, Michael; Horovitz, Amnon (2017) Sequential allosteric mechanism of ATP hydrolysis by the CCT/TRiC chaperone is revealed through Arrhenius analysis. Proc Natl Acad Sci U S A 114:5189-5194
Levitt, Michael; Levitt, Jonathan M (2017) Future of fundamental discovery in US biomedical research. Proc Natl Acad Sci U S A 114:6498-6503
Hosseinzadeh, Parisa; Bhardwaj, Gaurav; Mulligan, Vikram Khipple et al. (2017) Comprehensive computational design of ordered peptide macrocycles. Science 358:1461-1466
Lev, Bogdan; Murail, Samuel; Poitevin, Frédéric et al. (2017) String method solution of the gating pathways for a pentameric ligand-gated ion channel. Proc Natl Acad Sci U S A 114:E4158-E4167
Kang, Hongsuk; Vázquez, Francisco X; Zhang, Leili et al. (2017) Emerging ?-Sheet Rich Conformations in Supercompact Huntingtin Exon-1 Mutant Structures. J Am Chem Soc 139:8820-8827

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