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


ABSTRACT: We measured the transbilayer diffusion of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in large unilamellar vesicles, in both the gel (L?') and fluid (L?) phases. The choline resonance of headgroup-protiated DPPC exchanged into the outer leaflet of headgroup-deuterated DPPC-d13 vesicles was monitored using 1H 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 long-lived, submicron-sized holes resulting from incomplete surface coverage are the sites of rapid transbilayer movement.

SUBMITTER: Marquardt D 

PROVIDER: S-EPMC5397887 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

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<sup>1</sup>H NMR Shows Slow Phospholipid Flip-Flop in Gel and Fluid Bilayers.

Marquardt Drew D   Heberle Frederick A FA   Miti Tatiana T   Eicher Barbara B   London Erwin E   Katsaras John J   Pabst Georg G  

Langmuir : the ACS journal of surfaces and colloids 20170203 15


We measured the transbilayer diffusion of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in large unilamellar vesicles, in both the gel (L<sub>β'</sub>) and fluid (L<sub>α</sub>) phases. The choline resonance of headgroup-protiated DPPC exchanged into the outer leaflet of headgroup-deuterated DPPC-d13 vesicles was monitored using <sup>1</sup>H NMR spectroscopy, coupled with the addition of a paramagnetic shift reagent. This allowed us to distinguish between the inner and outer bilayer leafle  ...[more]

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