Anomalous and anisotropic nanoscale diffusion of hydration water molecules in fluid lipid membranes. Issue 42 (4th September 2015)

• Record Type: Journal Article
• Authors: Toppozini, Laura; Roosen-Runge, Felix; I. Bewley, Robert; M. Dalgliesh, Robert; Perring, Toby; Seydel, Tilo; Glyde, Henry R.; García Sakai, Victoria; Rheinstädter, Maikel C.
• Is Part Of: Soft matter. Volume 11:Issue 42(2015)
• Page Start: 8354
• Page End: 8371
• Publication Date: 2015-09-04
• Subjects: Soft condensed matter -- Periodicals; 530.413
• DOI: 10.1039/c5sm01713k
• Languages: English
• ISSNs: 1744-683X

Abstract

Abstract : We studied the dynamics of membrane hydration water in close proximity to a lipid bilayer using neutron scattering and computer modeling. We find the nanoscale motion of hydration water molecules to be anisotropic and anomalous. Abstract : We have studied nanoscale diffusion of membrane hydration water in fluid-phase lipid bilayers made of 1, 2-dimyristoyl-3-phosphocholine (DMPC) using incoherent quasi-elastic neutron scattering. Dynamics were fit directly in the energy domain using the Fourier transform of a stretched exponential. By using large, 2-dimensional detectors, lateral motions of water molecules and motions perpendicular to the membranes could be studied simultaneously, resulting in 2-dimensional maps of relaxation time, τ, and stretching exponent, β . We present experimental evidence for anomalous (sub-diffusive) and anisotropic diffusion of membrane hydration water molecules over nanometer distances. By combining molecular dynamics and Brownian dynamics simulations, the potential microscopic origins for the anomaly and anisotropy of hydration water were investigated. Bulk water was found to show intrinsic sub-diffusive motion at time scales of several picoseconds, likely related to caging effects. In membrane hydration water, however, the anisotropy of confinement and local dynamical environments leads to an anisotropy of relaxation times and stretched exponents, indicative of anomalous dynamics.