Searcharxiv⌕ Search

arXiv · 2610.09595

Multiscale Decoupling in Peptide-Membrane Interactions: From Elastic Softening to Domain-Mediated Stiffening

Abstract

Membrane composition plays a central role in determining how antimicrobial peptides (AMPs) interact with and alter the physical properties of lipid membranes. Here, we investigate the composition-dependent mechanical and structural response of lipid membranes to the AMP aurein using neutron spin-echo (NSE) spectroscopy, neutron membrane diffraction (NMD), and pressure (P)-area (A) isotherms, complemented by previously reported quasielastic neutron scattering (QENS) measurements. In a zwitterionic DMPC membrane, aurein induces progressive softening, manifested by a concentration-dependent decrease in both the bending rigidity and area compressibility modulus. NMD reveals a slight bilayer thinning but no prominent peptide-associated contribution within the deuterated hydrocarbon region, indicating that the progressive mechanical softening is not accompanied by increasingly deep peptide penetration into the hydrophobic core. In contrast, anionic phosphatidylglycerol (PG)-containing DMPC/DMPG membranes exhibit a non-monotonic response, with initial softening followed by pronounced stiffening at higher peptide concentrations. Complementary P-A isotherm measurements independently reproduce these contrasting mechanical responses, showing progressive softening of DMPC but stiffening of DMPC/DMPG. Most importantly, the combined NSE and QENS results reveal a striking multiscale decoupling: aurein suppresses molecular-scale lipid lateral diffusion while simultaneously reducing collective membrane stiffness at the mesoscopic scale, demonstrating that molecular lipid dynamics and collective membrane mechanics can evolve in opposite directions under the same peptide perturbation.Together, these results show that membrane composition governs the collective mechanical response to aurein, while molecular lipid dynamics can respond independently at shorter length and time scales.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Veerendra K. Sharma, Shuo Qian, Gergely Nagy, Sonam Raghav, Sajal K. Ghosh. 2026-10-07. Multiscale Decoupling in Peptide-Membrane Interactions: From Elastic Softening to Domain-Mediated Stiffening. https://arxiv.org/abs/2610.09595

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Cell size and confinement drive asymmetric cell division through a cortical instability

Asymmetric cell division -- in which a mother cell divides into two daughter cells of unequal size -- is a fundamental problem in biology. It is believed that the asymmetry originates from the prior polarization of the mother cell. Here we show that division asymmetry can occur spontaneously even in unpolarized mother cells. Specifically, curvature-dependent active stresses in the cell cortex can lead to this symmetry breaking without any molecular polarity cue if the mother cell is confined within a restricted space. Either reducing the cell size or tightening mechanical confinement triggers the same spontaneous symmetry-breaking instability, in which the contractile ring slips off the equator to yield daughters of unequal volume. In the presence of a polarity cue, this instability cooperates with the cue to program the division asymmetry. The model prediction is compared with the imaging data of C. elegans embryogenesis, in which successive cell divisions in a confined eggshell lead to smaller and smaller cell sizes. The measured division asymmetry indeed increases as the cells shrink, and is further amplified when the embryo is mechanically compressed, both in agreement with the model prediction.

cond-mat.soft↗

Laser fragmentation in liquid - constructing a generic reaction map

Excitation of absorbing colloids in liquid by pulsed laser irradiation creates highly non-equilibrium states of matter that relax via defined pathways of thermal and non-thermal dissipation channels. The structural fingerprint of these channels can be probed by ultrafast {\it in situ} x-ray scattering methods and classified as a function of temporal delay of excitation excitation density, or specifically laser fluence. We study the example of photo-excitation of a gold colloid by picosecond laser pulses at the interband absorption band at 400 nm in water. By quantifying lattice temperature, crystalline fraction, particle sizes and the structural response of the water around the nanoparticles a reaction map is constructed that allows to pinpoint heating, particle melting, water bubble formation and finally particle fragmentation to form nanoclusters of predominant sizes of < 3 nm for applications in theranostics, photonics or catalysis.

cond-mat.soft↗

Scallop Theorem for Swimming in Anisotropic Fluids

In isotropic fluids like water, micrometer-scale swimmers have evolved swim strokes to translate despite their tiny size. As described by Purcell in his Scallop Theorem, reciprocal motions, like those performed by a scallop, cannot drive swimming when inertial effects are absent, as is typical at micrometer length scales. Thus, microswimmers have evolved complex structures that can perform non-reciprocal swim strokes or body displacements to generate motion. Microswimmer dynamics in structured fluids differ fundamentally from those in isotropic fluids because of their inherent asymmetry. The orientation of elongated constituents and the topological defects that spontaneously form near microswimmers provide broken symmetries, even atequilibrium. This is sufficient for the dynamic disturbance of even the simplest isotropic swimmers to generate propulsion. We combine experiments on magnetically rotated colloids in nematic liquid crystals with analytic non-equilibrium solutions to formulate propulsion strategies for microswimmers in nematic fluids and determine how swimming velocity depends on the rotation rate, materials parameters, and forcing regimes. For example, we find that micro-scale spherical colloids swim effectively under continuous rotation and under reciprocal forcing.Thus, swim strokes that are ineffective in isotropic fluids are highly effective in nematic liquid crystals. In light of these observations, the Scallop Theorem is extended for structured fluids.

cond-mat.soft↗