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This article is cited in 2 scientific papers (total in 2 papers)
ANALYSIS AND MODELING OF COMPLEX LIVING SYSTEMS
Molecular dynamics assessment of the mechanical properties of fibrillar actin
N. A. Koubassova, A. K. Tsaturyan Институт механики МГУ,
Россия, 119192, Москва, Мичуринский проспект, д. 1
Abstract:
Actin is a conserved structural protein that is expressed in all eukaryotic cells. When polymerized, it forms long filaments of fibrillar actin, or F-actin, which are involved in the formation of the cytoskeleton, in muscle contraction and its regulation, and in many other processes. The dynamic and mechanical properties of actin are important for interaction with other proteins and the realization of its numerous functions in the cell. We performed 204.8 ns long molecular dynamics (MD) simulations of an actin filament segment consisting of 24 monomers in the absence and the presence of MgADPat 300 K in the presence of a solvent and at physiological ionic strength using the AMBER99SB-ILDN and CHARMM36 force fields in the GROMACS software environment, using modern structural models as the initial structure obtained by high-resolution cryoelectron microscopy. MD calculations have shown that the stationary regime of fluctuations in the structure of the F-actin long segment is developed 80–100 ns after the start of the MD trajectory. Based on the results of MD calculations, the main parameters of the actin helix and its bending, longitudinal, and torsional stiffness were estimated using a section of the calculation model that is far enough away from its ends. The estimated subunit axial (2.72–2.75 nm) and angular (165–168$^\circ$) translation of the F-actin helix, its bending (2.8–4.7$\cdot$ 10$^{-26}$ N$\cdot$m$^2$), longitudinal (36–47$\cdot$ 10$^{-9}$ N), and torsional (2.6–3.1$\cdot$ 10$^{-26}$ N$\cdot$m$^2$) stiffness are in good agreement with the results of the most reliable experiments. The results of MD calculations have shown that modern structural models of F-actin make it possible to accurately describe its dynamics and mechanical properties, provided that computational models contain a sufficiently large number of monomers, modern force fields, and relatively long MD trajectories are used. The inclusion of actin partner proteins, in particular, tropomyosin and troponin, in the MD model can help to understand the molecular mechanisms of such important processes as the regulation of muscle contraction.
Keywords:
F-actin, MgADP, mathematical modeling, molecular dynamics, flexural, longitudinal, and torsional stiffness.
Received: 27.06.2022 Revised: 19.08.2022 Accepted: 29.08.2022
Citation:
N. A. Koubassova, A. K. Tsaturyan, “Molecular dynamics assessment of the mechanical properties of fibrillar actin”, Computer Research and Modeling, 14:5 (2022), 1081–1092
Linking options:
https://www.mathnet.ru/eng/crm1019 https://www.mathnet.ru/eng/crm/v14/i5/p1081
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Abstract page: | 97 | Full-text PDF : | 36 | References: | 20 |
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