Magainin 2 and PGLa in bacterial membrane mimics III : membrane fusion and disruption

We previously speculated that the synergistically enhanced antimicrobial activity of Magainin 2 and PGLa is related to membrane adhesion, fusion, and further membrane remodelling. Here, we combined computer simulations with time-resolved in vitro fluorescence microscopy, cryogenic electron microscopy (cryo-EM), and small-angle X-ray scattering (SAXS) to interrogate such morphological and topological changes of vesicles at nanoscopic and microscopic length scales in real time. Coarse-grained simulations revealed the formation of an elongated and bent fusion zone between vesicles in the presence of equimolar peptide mixtures. Vesicle adhesion and fusion was observed to occur within few seconds by cryo-EM and corroborated by SAXS measurements. The latter experiments further indicated continued and time-extended structural remodelling also for individual peptides or chemically-linked peptide heterodimers, but with different kinetics. Fluorescence microscopy further captured peptide-dependent adhesion, fusion, and occasional bursting of giant unilamellar vesicles already few seconds after peptide addition. The synergistic interactions between the peptides shorten the time response of vesicles and enhance membrane fusogenic and disrupting properties of the equimolar mixture compared to the individual peptides

Heterogeneous relaxation dynamics of nano-confined salol probed by DMA

We present novel low-frequency (0.1 Hz$\hbox{--}$50 Hz) measurements of the complex elastic susceptibility of the glass-forming liquid salol confined to nanoporous Vycor glass. Our data can be perfectly interpreted with the assumption of a radial distribution of Vogel-Fulcher temperatures $T_{0}(r)$ inside the pores, resulting from an increase of the molecular relaxation time with decreasing distance from the rough pore surface as recently found by computer simulations (Scheidler et al., Europhys. Lett. 59, 701 (2002)). The results show for the first time, that the dynamic elastic response is extremely sensitive for separating confinement-induced acceleration effects of the molecular dynamics and surface-induced slowing-down due to rough pore interfaces