CHARMM (Chemistry at Harvard Macromolecular Mechanics) has been a primary research tool for macromolecular simulation and modeling in biology for nearly three decades. During this period CHARMM development, applications emerging from its use have defined the field of biomolecular computation. This proposal is aimed at ensuring that CHARMM will continue as the development platform for future generations of scientists by addressing components of the software and its attendant support infrastructure that represent bottlenecks in development, performance and maintenance. Specifically, continued refactoring of the code will provide improvements and extensions to underlying computational kernels in CHARMM, which will significantly enhance single processor performance and improve parallel scaling. Additional developments will establish a more extensive and user friendly front end for complex simulation preparation using CHARMM-GUI (www.charmm-gui.org) and embracing the emerging big data as drivers of biological simulations approaching cellular level modeling. Emphasis will be given to improving parallelism and accelerated simulations by extending the new and successful DOMDEC kernels for scalable parallel applications, migrating more of CHARMM exceptional functionality to GPU-based accelerators through both DOMDEC and the CHARMM/OpenMM interfaces. Additionally, we will focus on the establishment of a scalable simulation architecture for systems approaching hundreds of millions of particles utilizing both detailed atomic as well as coarse-grained models. The outcome of these efforts will be a program platform that will facilitate continued forefront research in macromolecular simulation and modeling and enable its continued development and maintenance for future generations of researchers.

Public Health Relevance

CHARMM (Chemistry at Harvard Macromolecular Mechanics) has been a primary research tool for macromolecular simulation and modeling in biology for nearly three decades, assisting biomedical researchers in theoretical investigations of protein/nucleic acid-ligand interactions, enzyme mechanism, protein/nucleic acid folding, free energy and docking simulations for drug discovery and design, and a large range of other applications in protein, nucleic acid, carbohydrate and membrane modeling. The more than 25,000 citations to CHARMM attest to the pivotal role that this software package and force field has in the biomedical community. The aims of this proposal are to continue to modernize, improve performance, enable the utilization of large data as a key contributor to macromolecular modeling, maintain to a solid pathway for continued development of the CHARMM package to ensure its ongoing availability for biomedical researchers, and establish a more extensive and user friendly front-end for complex simulation preparation using CHARMM-GUI.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM103695-11
Application #
9502987
Study Section
Biodata Management and Analysis Study Section (BDMA)
Program Officer
Lyster, Peter
Project Start
2007-04-01
Project End
2020-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
11
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Heo, Lim; Feig, Michael (2018) PREFMD: a web server for protein structure refinement via molecular dynamics simulations. Bioinformatics 34:1063-1065
Nawrocki, Grzegorz; Karaboga, Alp; Sugita, Yuji et al. (2018) Effect of protein-protein interactions and solvent viscosity on the rotational diffusion of proteins in crowded environments. Phys Chem Chem Phys :
Hayes, Ryan L; Vilseck, Jonah Z; Brooks 3rd, Charles L (2018) Approaching protein design with multisite ? dynamics: Accurate and scalable mutational folding free energies in T4 lysozyme. Protein Sci 27:1910-1922
Feig, Michael; Yu, Isseki; Wang, Po-Hung et al. (2017) Crowding in Cellular Environments at an Atomistic Level from Computer Simulations. J Phys Chem B 121:8009-8025
Nawrocki, Grzegorz; Wang, Po-Hung; Yu, Isseki et al. (2017) Slow-Down in Diffusion in Crowded Protein Solutions Correlates with Transient Cluster Formation. J Phys Chem B 121:11072-11084
Hsu, Pin-Chia; Bruininks, Bart M H; Jefferies, Damien et al. (2017) CHARMM-GUI Martini Maker for modeling and simulation of complex bacterial membranes with lipopolysaccharides. J Comput Chem 38:2354-2363
Kim, Seonghoon; Lee, Jumin; Jo, Sunhwan et al. (2017) CHARMM-GUI ligand reader and modeler for CHARMM force field generation of small molecules. J Comput Chem 38:1879-1886
Arthur, Evan J; Brooks 3rd, Charles L (2016) Efficient implementation of constant pH molecular dynamics on modern graphics processors. J Comput Chem 37:2171-80
Lee, Jumin; Cheng, Xi; Swails, Jason M et al. (2016) CHARMM-GUI Input Generator for NAMD, GROMACS, AMBER, OpenMM, and CHARMM/OpenMM Simulations Using the CHARMM36 Additive Force Field. J Chem Theory Comput 12:405-13
Gagnon, Jessica K; Law, Sean M; Brooks 3rd, Charles L (2016) Flexible CDOCKER: Development and application of a pseudo-explicit structure-based docking method within CHARMM. J Comput Chem 37:753-62

Showing the most recent 10 out of 14 publications