1H NMR Shows Slow Phospholipid Flip-Flop in Gel and Fluid Bilayers

被引:95
|
作者
Marquardt, Drew [1 ,2 ]
Heberle, Frederick A. [3 ,5 ,6 ]
Miti, Tatiana [8 ]
Eicher, Barbara [1 ,2 ]
London, Erwin [9 ]
Katsaras, John [3 ,4 ,6 ,7 ]
Pabst, Georg [1 ,2 ]
机构
[1] Karl Franzens Univ Graz, Inst Mol Biosci, Biophys Div, NAWI Graz, A-8010 Graz, Austria
[2] BioTechMed Graz, A-8010 Graz, Austria
[3] Univ Tennessee, Bredesen Ctr, Knoxville, TN 37996 USA
[4] Univ Tennessee, Dept Phys & Astron, Knoxville, TN 37996 USA
[5] Oak Ridge Natl Lab, Joint Inst Biol Sci, Oak Ridge, TN 37831 USA
[6] Oak Ridge Natl Lab, Biol & Soft Matter Div, Oak Ridge, TN 37831 USA
[7] Oak Ridge Natl Lab, Shull Wollan Ctr Joint Inst Neutron Sci, Oak Ridge, TN 37831 USA
[8] Univ S Florida, Dept Phys, Tampa, FL 33620 USA
[9] Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
基金
美国国家科学基金会; 奥地利科学基金会;
关键词
LARGE UNILAMELLAR VESICLES; ANGLE NEUTRON-SCATTERING; ATOMIC-FORCE MICROSCOPY; MAIN PHASE-TRANSITION; SUPPORTED BILAYERS; ANIONIC PHOSPHOLIPIDS; ASYMMETRIC VESICLES; EXCHANGE PROTEIN; LIPID ASYMMETRY; MEMBRANE;
D O I
10.1021/acs.langmuir.6b04485
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We measured the transbilayer diffusion of 1,2-dipahnitoyl-sn-glycero-3-phosphocholine (DPPC) in large unilamellar vesicles, in both the gel (L-beta') and fluid (L-alpha) phases. The chOline resonance of headgroup-protiated DPPC exchanged into the outer leaflet of headgroup-deuterated DPPC-d13 vesicles was monitored using H-1 NMR spectroscopy, coupled with the addition of a paramagnetiC shift reagent. This allowed us to distinguish between the inner and outer bilayer leaflet of DPPC, to determine the flip-flop rate as a function of 'temperature. Flip-flop of fluid-phase DPPC exhibited Arrhenius, kinetics, from which we determined an activation energy of 122 kJ mol(-1). In gel-phase DPPC vesicles, flip-flop was not observed over the course of 250 h. Our findings are in contrast to previous studies of solid-supported bilayers, where the reported DPPC translocation rates are at least several orders of magnitude faster than those in vesicles at corresponding temperatures. We reconcile these differences by proposing a defect-mediated acceleration of lipid translocation in supported bilayers, where longlived, submicron-sized holes resulting from incomplete surface coverage are the sites of rapid transbilayer movement.
引用
收藏
页码:3731 / 3741
页数:11
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