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Exploring the Mechanism of Alyteserin-1c in Gram-Positive and Gram-Negative Bacterial Membrane Models Using a
Akshay Sasidharan1, Rajasekaran Ramalingam1
1Quantitative Biology Lab, Department of Integrative Biology, School of Bio Sciences and Technology, Vellore Institute of Technology (VIT Deemed to be University), Vellore, Tamil Nadu, India.
Abstract:
Alyteserin-1c is a 23-amino-acid cationic antimicrobial peptide exhibiting greater activity against Gram-negative than Gram-positive bacteria (Conlon et al. 2009), yet the molecular basis of this differential membrane selectivity remains incompletely understood. Using all-atom molecular dynamics simulations (200 ns × 3 independent replicates per system), we examined the interactions of a pre-assembled Alyteserin-1c hexamer with simplified bilayer models representing Gram-positive (75% PG/25% PE) and Gram-negative (75% PE/25% PG) bacterial inner membranes. The hexameric assembly maintained structural stability and substantial α-helical content throughout all simulations, with oligomeric cohesion associated primarily with hydrophobic packing of residues L10, L13, V14, I17, and F6. Cationic residues K7 and K15 remained lipid-exposed with near-permanent headgroup contact occupancy, suggesting their role as principal membrane-anchoring sites. Comparative membrane analyses indicated greater lateral lipid mobility, lower bilayer density, and stronger local acyl chain perturbation in the Gram-negative membrane model, consistent with greater membrane susceptibility at lower peptide concentrations. Helix orientation and pore geometry analyses were inconsistent with stable barrel-stave transmembrane pore formation and instead supported interfacial or transient toroidal-like membrane perturbations. Transient single-file water threading was observed in the Gram-positive system, while perturbations in the Gram-negative membrane remained predominantly surface-localized. These findings provide a computationally derived mechanistic framework for the membrane selectivity of Alyteserin-1c and may inform rational design of membrane-targeting antimicrobial peptides. Given the simplified bilayer models, pre-assembled oligomeric assumption, and accessible simulation timescales, the proposed mechanisms should be interpreted as hypothesis-generating rather than definitive.
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