CORRELATION-FUNCTIONS FOR LIPID-MEMBRANE DYNAMICS OBTAINED FROM NMR-SPECTROSCOPY

Citation
Aa. Nevzorov et al., CORRELATION-FUNCTIONS FOR LIPID-MEMBRANE DYNAMICS OBTAINED FROM NMR-SPECTROSCOPY, Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics, 55(3), 1997, pp. 3276-3282
Citations number
33
Categorie Soggetti
Physycs, Mathematical","Phsycs, Fluid & Plasmas
ISSN journal
1063651X
Volume
55
Issue
3
Year of publication
1997
Part
B
Pages
3276 - 3282
Database
ISI
SICI code
1063-651X(1997)55:3<3276:CFLDOF>2.0.ZU;2-Q
Abstract
Nuclear magnetic resonance (NMR) studies of the spin relaxation of lip id membranes provide a powerful tool for investigating the dynamics of these important biological structural elements. Here spectral densiti es of motion for various dynamical models have been fitted to H-2 spin -lattice relaxation rates' (R(1Z)) measured for vesicles for 1,2-dimyr istoyl-sn-glycero-3-phosphocholine, in the liquid-crystalline state, o ver a broad frequency range (2.59-95.3 MHz; total of 15 magnetic-field strengths). Moreover, the corresponding C-13 R(1Z) values predicted f rom the models have been compared to experiment from 15.0 to 151 MHz, thereby enabling unification of the NMR relaxation data for bilayer li pids. A molecular diffusion model or alternatively a three-dimensional collective fluctuation model describes best the 2H and C-13 R(1Z) dat a. To emphasize the universality of this approach, the models have als o been fitted to C-13 R(1Z) data for vesicles of 1,2-dipalmitoyl-sn-gl ycero-3-phosphocholine (15.0-151 MHz; eight magnetic field strengths), and the H-2 R(1Z) values for the corresponding multilamellar dispersi ons theoretically predicted. Correlation functions have been calculate d for the lipid reorientations from the analysis of NMR relaxation dat a. The results suggest that slower motions are predominant in the low to mid megahertz range due to noncollective molecular motions or therm al collective excitations, whereas the bilayer interior corresponds to liquid hydrocarbon. The reorientational correlation functions derived from NMR spectroscopy are compared to recent molecular-dynamics simul ations of bilayer lipids in the fluid phase.