Complex biomembrane mimetics on the sub-nanometer scale

被引:12
|
作者
Heberle F.A. [1 ,2 ]
Pabst G. [3 ,4 ]
机构
[1] The Bredesen Center, University of Tennessee, Knoxville, 37996, TN
[2] Joint Institute for Biological Sciences and Biology and Soft Matter Division, Oak Ridge National Laboratory, Oak Ridge, 37831, TN
[3] Institute of Molecular Biosciences, Biophysics Division, NAWI Graz, University of Graz, Graz
[4] BioTechMed-Graz, Graz
基金
奥地利科学基金会;
关键词
Asymmetric bilayers; Intermembrane interactions; Lipid domains; Lipid flip-flop; Lipid-protein interactions; Small-angle neutron and X-ray scattering;
D O I
10.1007/s12551-017-0275-5
中图分类号
学科分类号
摘要
Biomimetic lipid vesicles are indispensable tools for gaining insight into the biophysics of cell physiology on the molecular level. The level of complexity of these model systems has steadily increased, and now spans from domain-forming lipid mixtures to asymmetric lipid bilayers. Here, we review recent progress in the development and application of elastic neutron and X-ray scattering techniques for studying these systems in situ and under physiologically relevant conditions on the nanometer to sub-nanometer length scales. In particular, we focus on: (1) structural details of coexisting liquid-ordered and liquid-disordered domains, including their thickness and lipid packing mismatch as a function of a size transition from nanoscopic to macroscopic domains; (2) membrane-mediated protein partitioning into lipid domains; (3) the role of the aqueous medium in tuning interactions between membranes and domains; and (4) leaflet-specific structure in asymmetric bilayers and passive lipid flip-flop. © 2017, The Author(s).
引用
收藏
页码:353 / 373
页数:20
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