Korhonen A, Jauhiainen M, Ehnholm C, Kovanen P T, Ala-Korpela M
Department of Physical Sciences, University of Oulu, Finland.
Biochem Biophys Res Commun. 1998 Aug 28;249(3):910-6. doi: 10.1006/bbrc.1998.9162.
There is evidence that phospholipid transfer protein (PLTP) can increase reverse cholesterol transport by inducing favorable subclass distribution in the high density lipoprotein (HDL) fraction. This includes generation of initial cholesterol acceptor particles, pre beta-HDL, and of enlarged particles that are rapidly cleared from the circulation. However, partly because of methodological difficulties, the mechanisms behind the PLTP-mediated interconversion of HDL particles are not fully understood. In this communication, we describe the use of a novel methodology, based on 1H NMR spectroscopy, to study the PLTP-induced size changes in the HDL particles. In accordance with native gradient gel electrophoresis, the 1H NMR data revealed a gradual production of enlarged HDL particles in the HDL3+ PLTP mixtures. In addition, according to a physical model for lipoprotein particles, relating the frequency shifts observable with NMR to the size of the lipoprotein particles, the NMR data demonstrated that PLTP-mediated HDL remodeling involves fusion of the HDL particles.
有证据表明,磷脂转运蛋白(PLTP)可通过诱导高密度脂蛋白(HDL)组分中有利的亚类分布来增加逆向胆固醇转运。这包括生成初始胆固醇受体颗粒前β-HDL以及从循环中快速清除的增大颗粒。然而,部分由于方法上的困难,PLTP介导的HDL颗粒相互转化背后的机制尚未完全明了。在本通讯中,我们描述了一种基于1H核磁共振波谱的新方法的应用,以研究PLTP诱导的HDL颗粒大小变化。与天然梯度凝胶电泳一致,1H NMR数据显示在HDL3 + PLTP混合物中逐渐产生增大的HDL颗粒。此外,根据脂蛋白颗粒的物理模型,将NMR可观察到的频率变化与脂蛋白颗粒的大小相关联,NMR数据表明PLTP介导的HDL重塑涉及HDL颗粒的融合。