Surface Electrostatics of Lipid Bilayers by EPR of a pH-Sensitive Spin-Labeled Lipid

被引:17
|
作者
Voinov, Maxim A. [1 ]
Rivera-Rivera, Izarys [1 ]
Smirnov, Alex I. [1 ]
机构
[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PHOSPHATIDYLGLYCEROL BILAYERS; PHOSPHOLIPID-BILAYERS; MEMBRANE ELECTROSTATICS; BIOLOGICAL-MEMBRANES; PHASE-TRANSITION; POTENTIALS; CHARGE; ESR; SPECTROSCOPY; DISPERSIONS;
D O I
10.1016/j.bpj.2012.11.3806
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Many biophysical processes such as insertion of proteins into membranes and membrane fusion are governed by bilayer electrostatic potential. At the time of this writing, the arsenal of biophysical methods for such measurements is limited to a few techniques. Here we describe a, to our knowledge, new spin-probe electron paramagnetic resonance (ERR) approach for assessing the electrostatic surface potential of lipid bilayers that is based on a recently synthesized EPR probe (IMTSL-PTE) containing a reversibly ionizable nitroxide tag attached to the lipids' polar headgroup. ERR spectra of the probe directly report on its ionization state and, therefore, on electrostatic potential through changes in nitroxide magnetic parameters and the degree of rotational averaging. Further, the lipid nature of the probe provides its full integration into lipid bilayers. Tethering the nitroxide moiety directly to the lipid polar headgroup defines the location of the measured potential with respect to the lipid bilayer interface. Electrostatic surface potentials measured by EPR of IMTSL-PTE show a remarkable (within +/-2%) agreement with the Gouy-Chapman theory for anionic DMPG bilayers in fluid (48 degrees C) phase at low electrolyte concentration (50 nnM) and in gel (17 degrees C) phase at 150-mM electrolyte concentration. This agreement begins to diminish for DMPG vesicles in gel phase (17 degrees C) upon varying electrolyte concentration and fluid phase bilayers formed from DMPG/DMPC and POPG/POPC mixtures. Possible reasons for such deviations, as well as the proper choice of an electrostatically neutral reference interface, have been discussed. Described EPR method is expected to be fully applicable to more-complex models of cellular membranes.
引用
收藏
页码:106 / 116
页数:11
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