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Biology subjects

Blazhynska, M.

Publications and source records attributed to Blazhynska, M..

2 recordsLinked to original sources

Satellite Tobacco Mosaic Virus: Revealing Environmental Drivers of Capsid and Nucleocapsid Stability using High-Resolution Simulations

The Satellite Tobacco Mosaic Virus (STMV) serves as a model system for elucidating how electrostatic and mechanical forces shape single-stranded (ss) RNA viral architecture. Lever-aging a cumulative total of 1.5 {micro}s of simulation with a polarizable force field including 1.2 {micro}s of conventional Molecular Dynamics (MD) supplemented by Gaussian accelerated MD (GaMD), and well-tempered metadynamics (WTMetaD) enhanced sampling techniques, we examined how pH and ionic composition regulate the structural dynamics of preassembled STMV capsids. Six [~]1M-atom assemblies spanning physiological and stress-mimicking environments were modeled to capture the interplay among protein-protein, protein-RNA, and ion-mediated interactions. A representative GaMD trajectory, corresponding to the up to {micro}s-equivalent regime of conventional MD, revealed that the capsid undergoes coordinated radial fluctuations, with collective expansion and contraction of the icosahedral shell. WTMetaD free-energy surfaces, computed for all six assemblies, delineated distinct condition-specific minima, defining thermodynamically accessible conformations for each environment. During the early relaxation dynamics revealed in conventional MD, RNA-free capsids preserved their icosahedral symmetry in physiological salt, where monovalent ions screened intra-capsid electrostatics. RNA encapsidation further modulated this balance through divalent-ion coordination at the protein-RNA interface. Under acidic conditions, a reversible Na+/Mg2+ exchange reorganized interfacial charge networks while maintaining the overall capsid architecture. Transient chloride binding intermittently disrupted key inter-monomer salt bridges, exposing a regulatory mechanism for capsid plasticity and permeability. Our findings establish STMV as an inherently dynamic, ion-responsive structural assembly whose conformational adaptability emerges from finely balanced electrostatic coupling between the capsid and its RNA, providing an atomistic framework for how ssRNA icosahedral viruses sense and adjust to environmental changes.

biophysics↗

Water-Glycan Interactions Drive the SARS-CoV-2 Spike Dynamics: Insights into Glycan-Gate Control and Camouflage Mechanism

To develop therapeutic strategies against COVID-19, we introduce a high-resolution all-atom polarizable model capturing many-body effects of protein, glycans, solvent, and membrane components in SARS-CoV-2 spike protein open and closed states. Employing s-long molecular dynamics simulations powered by high-performance cloud-computing and unsupervised density-driven adaptive sampling, we investigated the differences in bulk-solvent-glycan and protein-solvent-glycan interfaces between these states. We unraveled a sophisticated solvent-glycan polarization interaction network involving the N165/N343 residues that provide structural support for the open state and identified key water molecules that could potentially be targeted to destabilize this configuration. In the closed state, the reduced solvent polarization diminishes the overall N165/N343 dipoles, yet internal interactions and a reorganized sugar coat stabilize this state. Despite variations, our glycan-solvent accessibility analysis reveals the glycan shield capability to conserve constant interactions with the solvent, effectively camouflaging the virus from immune detection in both states. The presented insights advance our comprehension of viral pathogenesis at an atomic level, offering potential to combat COVID-19.

biophysics↗