The broad objectives of this work are to provide new computer simulation tools that will enable the detailed analysis of the role of molecular diffusion in biological processes at the subcellular and cellular levels, and the application of these tools to selected problems where close contact with experimental work is possible. The diffusional encounter of molecules with enzymes, antibody molecules, receptors, or other proteins;with membranes;or with nucleic acids is centrally involved in metabolism, immune and nervous system functions, signal transduction, cytoskeletal remodeling, gene expression, and a host of other processes in biology. The goals of the next project period will be to extend our simulation methods to allow the study of such processes, and to apply such simulation methods to selected problems with an emphasis on increasing scales of space and time. The methods will help in the development of antiviral agents, neurological drugs, and other materials of medical importance.
The specific aims for the next project period include the following, (a) New methods will be developed for the unified treatment of polar and apolar interactions of diffusing molecules, (b) Coarse-grained models will be developed for detailed description of the internal motions of biopolymers and their intermolecular interactions in diffusional processes, (c) Continuum simulation methods for molecular diffusion will be developed as a complement to the more familiar Brownian dynamics simulation methods, (d) Applications will be made to study crowding effects relevant to antiviral drug action, and to study diffusion and reaction of neurotransmitter in model synapses. The public health relevance of this work lies in the fact that the methods to be developed will be useful in the computer-aided design of Pharmaceuticals, including monoclonal antibodies that rapidly bind to and inactivate viruses, and drugs that act at multiple sites within synapses. Training of undergraduate, graduate and postdoctoral students for careers in public health will continue to be a key aspect of the project.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031749-29
Application #
7885492
Study Section
Special Emphasis Panel (ZRG1-BCMB-Q (90))
Program Officer
Preusch, Peter C
Project Start
1983-06-01
Project End
2011-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
29
Fiscal Year
2010
Total Cost
$314,718
Indirect Cost
Name
University of California San Diego
Department
Pharmacology
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Guan, W; Cheng, X; Huang, J et al. (2018) RPYFMM: Parallel Adaptive Fast Multipole Method for Rotne-Prager-Yamakawa Tensor in Biomolecular Hydrodynamics Simulations. Comput Phys Commun 227:99-108
Jurrus, Elizabeth; Engel, Dave; Star, Keith et al. (2018) Improvements to the APBS biomolecular solvation software suite. Protein Sci 27:112-128
Huang, Yu-Ming M; Huber, Gary A; Wang, Nuo et al. (2018) Brownian dynamic study of an enzyme metabolon in the TCA cycle: Substrate kinetics and channeling. Protein Sci 27:463-471
Caliman, Alisha D; Miao, Yinglong; McCammon, James A (2018) Mapping the allosteric sites of the A2A adenosine receptor. Chem Biol Drug Des 91:5-16
Utesch, Tillmann; de Miguel Catalina, Alejandra; Schattenberg, Caspar et al. (2018) A Computational Modeling Approach Predicts Interaction of the Antifungal Protein AFP from Aspergillus giganteus with Fungal Membranes via Its ?-Core Motif. mSphere 3:
Zhang, Jingbo; Wang, Nuo; Miao, Yinglong et al. (2018) Identification of SLAC1 anion channel residues required for CO2/bicarbonate sensing and regulation of stomatal movements. Proc Natl Acad Sci U S A 115:11129-11137
Miao, Yinglong; McCammon, J Andrew (2018) Mechanism of the G-protein mimetic nanobody binding to a muscarinic G-protein-coupled receptor. Proc Natl Acad Sci U S A 115:3036-3041
Palermo, Giulia; Chen, Janice S; Ricci, Clarisse G et al. (2018) Key role of the REC lobe during CRISPR-Cas9 activation by 'sensing', 'regulating', and 'locking' the catalytic HNH domain. Q Rev Biophys 51:
Ricci, Clarisse G; Li, Bo; Cheng, Li-Tien et al. (2017) ""Martinizing"" the Variational Implicit Solvent Method (VISM): Solvation Free Energy for Coarse-Grained Proteins. J Phys Chem B 121:6538-6548
Dick, Benjamin L; Patel, Ashay; McCammon, J Andrew et al. (2017) Effect of donor atom identity on metal-binding pharmacophore coordination. J Biol Inorg Chem 22:605-613

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