Multiple mechanisms for critical behavior in the biologically relevant phase of lecithin bilayers

John F. Nagle, Horia I. Petrache, Nikolai Gouliaev, Stephanie Tristram-Nagle, Yufeng Liu, Robert M. Suter, and Klaus Gawrisch
Phys. Rev. E 58, 7769 – Published 1 December 1998
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Abstract

Lipid bilayer membranes manifest critical behavior in the lamellar D spacing observed by x-ray and neutron diffraction as the main phase transition is approached from the biologically relevant high temperature phase. The freezing out of conformational disorder of the hydrocarbon chains drives the main transition, but how this causes critical behavior of D(T) has been an interesting puzzle and various models are under investigation. This paper presents x-ray scattering and NMR data to test the various models. One model involves the straightforward lengthening of hydrocarbon chains as TM is approached, but it is shown that this accounts only for about half the anomalous increase in D. Another model of fluctuation induced expansion of the water region is shown to be inconsistent with two kinds of data. The first inconsistency is the lack of an increase in the Caillé fluctuation parameter η1. The second inconsistency is with D(T) data taken under osmotic pressure. Accurate simulations are employed to predict the theoretical values. A third model considers that the water spacing could expand because other interactions between bilayers may change as TM is approached, but there is no quantitative support for this model at present. A fourth model involving expansion of the headgroup region is tested with NMR data; results are qualitatively consistent but quantitatively inconclusive. While the precise mixture of models is still unresolved, it is concluded that multiple mechanisms must be operating in this critical regime.

  • Received 29 July 1998

DOI:https://doi.org/10.1103/PhysRevE.58.7769

©1998 American Physical Society

Authors & Affiliations

John F. Nagle1,2,*, Horia I. Petrache1, Nikolai Gouliaev1, Stephanie Tristram-Nagle2, Yufeng Liu1, Robert M. Suter1, and Klaus Gawrisch3

  • 1Department of Physics, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213
  • 2Department of Biological Science, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213
  • 3Laboratory of Membrane Biochemistry and Biophysics, NIAAA, National Institutes of Health, Rockville Maryland 20852

  • *Author to whom correspondence should be addressed. Electronic address: nagle+@andrew.cmu.edu

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Vol. 58, Iss. 6 — December 1998

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