Bioenergetic membranes are a key cellular apparatus that carry out a series of interlinked energy conversion processes providing ATP and key metabolites for a cell. The individual processes and their underlying membrane proteins have been investigated intensively, but rarely have the processes been studied together, in particular not on the scale of a full organelle. The reasons are both lack of whole-membrane atomic resolution models and huge complexity. In case of a rather primitive, yet still representative bioenergetic membrane, namely the photosynthetic chromatophore of purple bacteria, the overall structure has been recently described in atomic detail, also huge with an atom count of 100 million; however, computational tools and computer power are available today to investigate the system as a whole. This proposal seeks funds to study the chromatophore in several steps: (1) A 100 million atom model of an entire chromatophore is built and simulated through molecular dynamics to describe its key physical properties, such as quinol/quinone diffusion in the lipid phase as well as overall redox-state-dependent electrostatics. (2) Structural insight gained from this detailed simulation guides subsequent multiscale simulations of the membrane-wide charge transport via protein (cytochrome c2) and lipid (quinone/quinol) diffusion and binding. (3) Dynamics of insertion of key bioenergetic proteins into the membrane through the ribosome-linked insertase YidC and the coupling between the stator and rotor domains in ATP synthase are described through molecular dynamics. The proposed study will provide the groundwork for future membrane-wide investigations of bioenergetic and other cellular organelles.

Public Health Relevance

The chromatophore is a complex cellular machine, comprising hundreds of cooperating proteins embedded in a membrane organelle, performing vital energy harvesting and conversion processes fundamental to sustaining life. The chromatophore, even though it is a specialized organelle in photosynthetic bacterial cells, provides a prototype for more complex bioenergetic membrane systems such as mitochondria found in eukaryotic cells. The supramolecular structure of the chromatophore and its key components are now known to a degree not yet available for any other cell type, namely, in chemical detail; hence, this project seeks to investigate how the chromatophore integrates its energy transduction processes and to provide a basis for future all-atom studies of the more complex membrane domains found in human cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM067887-14
Application #
9325038
Study Section
Macromolecular Structure and Function D Study Section (MSFD)
Program Officer
Lyster, Peter
Project Start
2003-05-01
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
14
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Type
Organized Research Units
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Benson, Christopher R; Maffeo, Christopher; Fatila, Elisabeth M et al. (2018) Inchworm movement of two rings switching onto a thread by biased Brownian diffusion represent a three-body problem. Proc Natl Acad Sci U S A 115:9391-9396
Perilla, Juan R; Schulten, Klaus (2017) Physical properties of the HIV-1 capsid from all-atom molecular dynamics simulations. Nat Commun 8:15959
Perilla, Juan R; Zhao, Gongpu; Lu, Manman et al. (2017) CryoEM Structure Refinement by Integrating NMR Chemical Shifts with Molecular Dynamics Simulations. J Phys Chem B 121:3853-3863
Vermaas, Josh V; Pogorelov, Taras V; Tajkhorshid, Emad (2017) Extension of the Highly Mobile Membrane Mimetic to Transmembrane Systems through Customized in Silico Solvents. J Phys Chem B 121:3764-3776
Singharoy, Abhishek; Chipot, Christophe (2017) Methodology for the Simulation of Molecular Motors at Different Scales. J Phys Chem B 121:3502-3514
Hitchcock, Andrew; Hunter, C Neil; Sener, Melih (2017) Determination of Cell Doubling Times from the Return-on-Investment Time of Photosynthetic Vesicles Based on Atomic Detail Structural Models. J Phys Chem B 121:3787-3797
Singharoy, Abhishek; Chipot, Christophe; Moradi, Mahmoud et al. (2017) Chemomechanical Coupling in Hexameric Protein-Protein Interfaces Harnesses Energy within V-Type ATPases. J Am Chem Soc 139:293-310
Alvarez, Frances J D; He, Shaoda; Perilla, Juan R et al. (2017) CryoEM structure of MxB reveals a novel oligomerization interface critical for HIV restriction. Sci Adv 3:e1701264
Weisz, Daniel A; Liu, Haijun; Zhang, Hao et al. (2017) Mass spectrometry-based cross-linking study shows that the Psb28 protein binds to cytochrome b559 in Photosystem II. Proc Natl Acad Sci U S A 114:2224-2229
Goh, Boon Chong; Hadden, Jodi A; Bernardi, Rafael C et al. (2016) Computational Methodologies for Real-Space Structural Refinement of Large Macromolecular Complexes. Annu Rev Biophys 45:253-78

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