Rajaram O V, Sawyer W H
Russell Grimwade School of Biochemistry and Molecular Biology, University of Melbourne, Parkville, Victoria, Australia.
Biochem J. 1997 Feb 15;322 ( Pt 1)(Pt 1):159-65. doi: 10.1042/bj3220159.
This study reports the effects of charged lipids on the transfer of cholesterlyl-1 pyrene decanoate (Py-CE) between apolipoprotein-free microemulsion particles mediated by cholesteryl ester transfer protein (CETP). The surface charge characteristics of microemulsion particles composed of cholesteryl oleate and egg yolk phosphatidylcholine were altered by incorporating phosphatidyl-serine, oleate or stearylamine into the phosphatidylcholine that forms the surface monolayer of the particle. The transfer of Py-CE was measured continuously by following the decrease in excimer fluorescence that accompanies the transfer of the probe from donor to acceptor particles [Rajaram, Chan and Sawyer (1994) Biochem. J. 304, 423-430]. The inclusion of 20 mol% phosphatidylserine relative to the phospholipid in the surface monolayer of the emulsion caused a 64% decrease in the first-order rate constant describing the transfer. An increase in ionic strength caused a partial reversal of this effects, indicating that electrostatic factors are only partially responsible for the interaction with lipid. Complete inhibition of transfer was observed when 10 mol% sodium oleate was incorporated into the surface monolayer. The incorporation of stearylamine into the emulsion caused a 32% increase in the transfer rate. The binding of CETP to the different emulsion surfaces was also examined using a surface plasmon resonance biosensor. The presence of negatively charged lipid (phosphatidylserine or oleic acid) decreased the rate of association of CETP with the emulsion without a significant change in the dissociation rate constant. The presence of the positively charged lipid stearylamine increased the rate of association of CETP with the lipid surface. It is concluded that a negative surface charge on the monolayer decreases the rate of transfer by decreasing the affinity of CETP for these particles.
本研究报告了带电脂质对由胆固醇酯转运蛋白(CETP)介导的无载脂蛋白微乳液颗粒间胆固醇-1-芘癸酸酯(Py-CE)转移的影响。通过将磷脂酰丝氨酸、油酸或硬脂胺掺入形成颗粒表面单层的磷脂酰胆碱中,改变了由油酸胆固醇酯和蛋黄磷脂酰胆碱组成的微乳液颗粒的表面电荷特性。通过跟踪探针从供体颗粒转移到受体颗粒时伴随的准分子荧光减弱,连续测量Py-CE的转移[拉贾拉姆、陈和索耶(1994年)《生物化学杂志》304卷,423 - 430页]。相对于乳液表面单层中的磷脂,掺入20摩尔%的磷脂酰丝氨酸导致描述转移的一级速率常数降低了64%。离子强度的增加导致这种效应部分逆转,表明静电因素只是与脂质相互作用的部分原因。当在表面单层中掺入10摩尔%的油酸钠时观察到转移完全被抑制。将硬脂胺掺入乳液中导致转移速率增加了32%。还使用表面等离子体共振生物传感器检查了CETP与不同乳液表面的结合。带负电荷的脂质(磷脂酰丝氨酸或油酸)的存在降低了CETP与乳液的结合速率,而解离速率常数没有显著变化。带正电荷的脂质硬脂胺的存在增加了CETP与脂质表面的结合速率。得出的结论是,单层上的负表面电荷通过降低CETP对这些颗粒的亲和力来降低转移速率。