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Updated: Feb 28, 2026

Author Spotlight: Advancing Cell Membrane Biophysics - Exploring Interactions and Challenges Through Experimental and Computational Approaches

Author Spotlight: Advancing Cell Membrane Biophysics - Exploring Interactions and Challenges Through Experimental and Computational Approaches

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Simulaciones de Gran Escala de Membranas Externas de Micobacterias Revelan Redistribución de PDIM Dependiente de la

Bibek Acharya, Sudarshan Lammichane, Turner P Brown

bioRxiv : the preprint server for biology

|February 27, 2026

Abstract:

The mycobacterial outer membrane (MOM) constitutes an asymmetric permeability barrier that influences lipid organization and transport in Mycobacterium tuberculosis . In this study, we have developed MARTINI 3 coarse-grained (CG) lipid models of the MOM, incorporating α-mycolic acids, 5 different trehalose-based lipids, and PDIM (phthiocerol dimycocerosate). The CG models were parameterized and validated using all-atom simulations of symmetric inner- and outer-leaflet membranes, as well as fully asymmetric MOM models. Bonded parameters were optimized through an iterative refinement procedure targeting atomistic bonded distributions. The CG simulations show good agreement with the all-atom simulation data and available experimental measurements in terms of the membrane thickness, solvent accessible surface area, lipid density profiles, and the outer-leaflet-induced lipid disorder in α-mycolic acids at the inner leaflet. The model reproduces the temperature-dependent phase behavior of all-atom α-mycolic acid membranes. Using this model, we demonstrate that PDIM localization, diffusion, and aggregation are strongly modulated by membrane fluidity and lipid composition, with enhanced translocation and clustering in liquid disordered environments. Our CG MOM lipid models provide a validated platform for large-scale simulations of mycobacterial membranes and enable mechanistic studies of lipid organization, membrane dynamics, and protein-membrane and membrane-drug interactions.

Palabras clave:

membrana externa de micobacterias modelos de grano grueso dinámica de lípidos Mycobacterium tuberculosis diftiocerol dimicocerosato

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