Searcharxiv⌕ Search

arXiv subjects

Tim Salditt

Publications and source records attributed to Tim Salditt.

23 records · Page 2Linked to original sources

Nanosecond molecular relaxations in lipid bilayers studied by high energy resolution neutron scattering and in-situ diffraction

We report a high energy-resolution neutron backscattering study to investigate slow motions on nanosecond time scales in highly oriented solid supported phospholipid bilayers of the model system DMPC -d54 (deuterated 1,2-dimyristoyl-sn-glycero-3-phoshatidylcholine), hydrated with heavy water. Wave vector resolved quasi-elastic neutron scattering (QENS) is used to determine relaxation times $τ$, which can be associated with different molecular components, i.e., the lipid acyl chains and the interstitial water molecules in the different phases of the model membrane system. The inelastic data are complemented both by energy resolved and energy integrated in-situ diffraction. From a combined analysis of the inelastic data in the energy and time domain, the respective character of the relaxation, i.e., the exponent of the exponential decay is also determined. From this analysis we quantify two relaxation processes. We associate the fast relaxation with translational diffusion of lipid and water molecules while the slow process likely stems from collective dynamics.

cond-mat.soft↗

Dispersion relation of lipid membrane shape fluctuations by neutron spin-echo spectrometry

We have studied the mesoscopic shape fluctuations in aligned multilamellar stacks of DMPC bilayers using the neutron spin-echo technique. The corresponding in plane dispersion relation $τ^{-1}$(q$_{||}$) at different temperatures in the gel (ripple, P$_{β'}$) and the fluid (L$_α$) phase of this model system has been determined. Two relaxation processes, one at about 10ns and a second, slower process at about 100ns can be quantified. The dispersion relation in the fluid phase is fitted to a smectic hydrodynamic theory, with a correction for finite q$_z$ resolution. We extract values for, the bilayer bending rigidity $κ$, the compressional modulus of the stacks $B$, and the effective sliding viscosity $η_3$. The softening of a mode which can be associated with the formation of the ripple structure is observed close to the main phase transition.

cond-mat.soft↗

Molecular motions in lipid bilayers studied by the neutron backscattering technique

We report a high energy-resolution neutron backscattering study to investigate slow motions on nanosecond time scales in highly oriented solid supported phospholipid bilayers of the model system DMPC -d54 (deuterated 1,2-dimyristoyl-sn-glycero-3-phoshatidylcholine), hydrated with heavy water. This technique allows to discriminate the onset of mobility at different length scales for the different molecular components, as e.g.\@ the lipid acyl-chains and the hydration water in between the membrane stacks, respectively, and provides a benchmark test regarding the feasibility of neutron backscattering investigations on these sample systems. We discuss freezing of the lipid acyl-chains, as observed by this technique, and observe a second freezing transition which we attribute to the hydration water.

cond-mat.soft↗

Probing Dynamics at Interfaces: Options for Neutron and X-ray Spectroscopy

Inelastic neutron and X-ray scattering experiments on surfaces and interfaces are a challenging topic in modern physics. Particular interest arises regarding surfaces and interfaces of soft matter and biological systems. We review both neutron and x-ray spectroscopic techniques with view at their applicability to these samples. We discuss the different methods, namely neutron triple-axis, backscattering and spin-echo spectroscopy as well as x-ray photon correlation spectroscopy, in the context of planar lipid membrane models as an example. By the combination of the different methods, a large range in momentum and energy transfer is accessible.

physics.bio-ph↗

Probing Dynamics at Interfaces: Molecular Motions in Lipid Bilayers studied by Neutron Backscattering

Lipid membranes in a physiological context cannot be understood without taking into account their mobile environment. Here, we report on a high energy-resolution neutron backscattering study to investigate slow motions on nanosecond time scales in highly oriented solid supported phospholipid bilayers of the model system DMPC -d54 (deuterated 1,2-dimyristoyl-sn-glycero-3-phoshatidylcholine). This technique allows discriminating the Q-dependent onset of mobility and provides a benchmark test regarding the feasibility of dynamical neutron scattering investigations on these sample systems. Apart from freezing of the lipid acyl-chains, we could observe a second freezing temperature that we attribute to the hydration water in between the membrane stacks. The freezing is lowered several degrees as compared to (heavy) bulk water.

physics.bio-ph↗