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Sequential Water and Headgroup Merger: Membrane Poration Paths and Energetics from MD Simulations. | LitMetric

Sequential Water and Headgroup Merger: Membrane Poration Paths and Energetics from MD Simulations.

Biophys J

Department of Theoretical and Computational Biophysics, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany. Electronic address:

Published: December 2020

AI Article Synopsis

Article Abstract

Membrane topology changes such as poration, stalk formation, and hemifusion rupture are essential to cellular function, but their molecular details, energetics, and kinetics are still not fully understood. Here, we present a unified energetic and mechanistic picture of metastable pore defects in tensionless lipid membranes. We used an exhaustive committor analysis to test and select optimal reaction coordinates and also to determine the nucleation mechanism. These reaction coordinates were used to calculate free-energy landscapes that capture the full process and end states. The identified barriers agree with the committor analysis. To enable sufficient sampling of the complete transition path for our molecular dynamics simulations, we developed a "gizmo" potential biasing scheme. The simulations suggest that the essential step in the nucleation is the initial merger of lipid headgroups at the nascent pore center. To facilitate this event, an indentation pathway is energetically preferred to a hydrophobic defect. Continuous water columns that span the indentation were determined to be on-path transients that precede the nucleation barrier. This study gives a quantitative description of the nucleation mechanism and energetics of small metastable pores and illustrates a systematic approach to uncover the mechanisms of diverse cellular membrane remodeling processes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822740PMC
http://dx.doi.org/10.1016/j.bpj.2020.10.037DOI Listing

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