Work

Membrane Lipid Composition and Asymmetry Modulate Translocation Versus Leakage of the Model Amphipathic Peptide MAP

Year: 2026

Type: article

Abstract: Cell-penetrating peptides (CPPs) can enable intracellular access while avoiding cytotoxicity, yet their behavior is highly sensitive to membrane composition. Here we show that lipid composition and leaflet asymmetry act as a switch that determines whether the amphipathic CPP MAP undergoes nondisruptive translocation or stabilizes membrane pores that drive leakage. Using high-field computational electrophysiology (CompEL) simulations in membranes of increasing physiological relevance, we show that electrically induced membrane defects allow the insertion of MAP peptides. We find symmetric anionic bilayers favor MAP insertion coupled to transmembrane pore stabilization in POPC/POPG membranes, reproducing progressive dye release in liposome leakage assays. Incorporation of cholesterol reduces the number of inserted peptides and conducts to faster leakage kinetics in cholesterol-containing vesicles. In contrast, a minimal asymmetric membrane model (POPC extracellular leaflet; POPC/POPS intracellular leaflet) supports MAP translocation without sustained membrane disruption. This delivery-relevant mechanism is supported by efficient MAP internalization in HEK293 cells while maintaining high viability. Polarized ATR–FTIR provides structural context, indicating predominantly membrane-associated α-helical conformations across lipid compositions. Together, these results establish lipid asymmetry and composition as actionable biointerface parameters that tune CPP function between translocation and leakage and demonstrate an experimentally benchmarked framework for predicting membrane outcomes across complex lipid environments.

Source: Journal of Chemical Information and Modeling

DOI: 10.1021/acs.jcim.6c01742