Temperature dependence of DMPC/DHPC mixing in a bicellar solution and its structural implications

Citation
E. Sternin et al., Temperature dependence of DMPC/DHPC mixing in a bicellar solution and its structural implications, LANGMUIR, 17(9), 2001, pp. 2610-2616
Citations number
34
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
17
Issue
9
Year of publication
2001
Pages
2610 - 2616
Database
ISI
SICI code
0743-7463(20010501)17:9<2610:TDODMI>2.0.ZU;2-J
Abstract
Bicelle-forming mixtures of short-chain 1,2-dicaproyl-sn-glycero-3-phosphoc holin (DHPC) and long-chain 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DM PC) exhibit complicated phase behavior. We studied chain-melting and morpho logical phase changes in mixtures of DMPC/DHPC of 4.5:1 molar ratio in the temperature range of 0-60 degreesC. The phase state of both lipids and the alignment of lipid monolayers in the magnetic field were determined by soli d-state H-2 and P-31 NMR. DMPC and DHPC mix in a micellar state at 0-10 deg reesC but separate upon heating to 15 degreesC into gel-phase DMPC bilayers and DHPC micelles. Near the gel-to-liquid-crystalline phase transition of DMPC, at 24 degreesC, the DHPC spectra become anisotropic suggesting arrang ement of DHPC in a mixed DMPC/DHPC phase. DMPC in this structure possesses the chain order typical of liquid crystalline bilayers, but DHPC chain orde r remains much lower, with lipid aggregates oriented mostly at random. In t he bicelle phase, at 32-36 degreesC, highly anisotropic lipid particles wit h their DMPC monolayer normal oriented perpendicular to the magnetic field are formed. The angular distribution function of bilayer normals has signif icant mosaic spread and tails with surprisingly high intensity that is caus ed by the monolayers that are oriented at random. In the bicelle phase, mag ic angle spinning nuclear Overhauser effect H-1 NMR spectrometry revealed i ntensive intermolecular cross-relaxation among DMPC and among DHPC molecule s but no detectable magnetization exchange between DMPC and DHPC, confirmin g that DHPC and DMPC experience limited physical contact. Above 36 degreesC , chain order of DMPC decreased, in particular for the bonds near the termi nal methyl groups, while order parameters of DHPC increased, both indicativ e for DMPC/DHPC mixing in the same monolayer. The degree of this mixed mono layer orientation at temperatures above the bicelle state is significantly lower. Near 60 degreesC a fraction of DHPC converts to a micellar phase tha t also dissolves a trace of DMPC. Thus, a highly aligned bicelle phase exis ts only in a narrow range of temperatures. Complex orientational distributi ons arise at other temperatures, driven by lipid mixing and structural phas e changes.