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小单层囊泡与固体支持物上的单双层之间的脂质转移:具有不对称脂质分布的支持双层的自组装。

Lipid transfer between small unilamellar vesicles and single bilayers on a solid support: self-assembly of supported bilayers with asymmetric lipid distribution.

作者信息

Reinl H M, Bayerl T M

机构信息

Technische Universität München, Physik Department E22, Garching, Germany.

出版信息

Biochemistry. 1994 Nov 29;33(47):14091-9. doi: 10.1021/bi00251a018.

Abstract

The transfer of lipids between small unilamellar vesicles of either dimyristoylphosphatidylcholine (DMPC), dimyristoylphosphatidylglycerol (DMPG), or dioctadecyl diammonium bromide (DODAB) and a single bilayer on a solid support of chain perdeuterated DMPC-d54 has been studied by time-resolved ATR infrared spectroscopy, deuterium NMR, and DSC. The IR method was used for measuring the transfer kinetics and the amount of lipid transferred to the supported bilayer, while NMR was employed for the assessment of molecular order and for the occurrence of lipid asymmetries due to the transfer. We find that the composition of a supported planar dimyristoylphosphatidylcholine (DMPC-d54) bilayer can be modified by incubation with high concentrations of sonicated vesicles consisting of the donor lipid. Three cases were studied. First, the incubation was done with DMPC as donor lipid. The kinetics of this process is double exponential and comparatively slow, with a half-time in the range of several hours. The activation energy was estimated as 50 +/- 2 kJ/mol. In a second set of measurements, cationic DODAB or anionic DMPG was used as donor lipid. The kinetics of this transfer is 1 order of magnitude faster than for DMPC and can be described by a single exponential. For DMPG transfer, we obtained an activation energy of 35 +/- 2 kJ/mol. Independent of the headgroup charge of the donor lipid, 25-35% of the (acceptor) DMPC in the supported bilayer is not accessible for exchange with the donor lipid. The transfer of either DMPG or DODAB causes drastic changes of the phase transition behavior of the supported bilayer without significantly altering the lipid packing density of the lipids.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过时间分辨衰减全反射红外光谱、氘核磁共振和差示扫描量热法,研究了二肉豆蔻酰磷脂酰胆碱(DMPC)、二肉豆蔻酰磷脂酰甘油(DMPG)或二辛基二甲基溴化铵(DODAB)的小单层囊泡与链全氘代DMPC-d54固体支持物上的单分子层之间的脂质转移。红外方法用于测量转移动力学和转移到支持单分子层的脂质数量,而核磁共振用于评估分子有序性以及由于转移导致的脂质不对称性的发生。我们发现,通过与由供体脂质组成的高浓度超声处理囊泡孵育,可以改变支持的平面二肉豆蔻酰磷脂酰胆碱(DMPC-d54)单分子层的组成。研究了三种情况。首先,以DMPC作为供体脂质进行孵育。该过程的动力学是双指数的且相对较慢,半衰期在数小时范围内。活化能估计为50±2 kJ/mol。在第二组测量中,使用阳离子DODAB或阴离子DMPG作为供体脂质。这种转移的动力学比DMPC快1个数量级,并且可以用单指数描述。对于DMPG转移,我们获得的活化能为35±2 kJ/mol。与供体脂质的头基电荷无关,支持单分子层中25 - 35%的(受体)DMPC无法与供体脂质进行交换。DMPG或DODAB的转移都会导致支持单分子层的相变行为发生剧烈变化,而不会显著改变脂质的堆积密度。(摘要截断于250字)

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