Gan Chaoye, Wang Zhexuan, Chen Yong
Nanoscale Science and Technology Laboratory, Institute for Advanced Study, Nanchang University, Nanchang, Jiangxi 330031, PR China; College of Life Sciences, Nanchang University, Nanchang, Jiangxi 330031, PR China.
Nanoscale Science and Technology Laboratory, Institute for Advanced Study, Nanchang University, Nanchang, Jiangxi 330031, PR China.
Atherosclerosis. 2017 Apr;259:5-11. doi: 10.1016/j.atherosclerosis.2017.02.022. Epub 2017 Feb 24.
BACKGROUND AND AIMS: The major apolipoproteins of plasma lipoproteins play vital roles in the structural integrity and physiological functions of lipoproteins. More than ten structural models of apolipoprotein A-I (apoA-I), the major apolipoprotein of high-density lipoprotein (HDL), have been developed successively. In these models, apoA-I was supposed to organize in a ring-shaped form. To date, however, there is no direct evidence under physiological condition. METHODS: Here, atomic force microscopy (AFM) was used to in situ visualize the organization of apoA-I, which was exposed via depletion of the lipid component of plasma HDL pre-immobilized on functionalized mica sheets. RESULTS: For the first time, the ring-shaped coarse structure and three detailed structures (crescent-shaped, gapped "O"-shaped, and parentheses-shaped structures, respectively) of apoA-I in plasma HDL, which have the ability of binding scavenger receptors, were directly observed and quantitatively measured by AFM. The three detailed structures probably represent the different extents to which the lipid component of HDL was depleted. Data on lipid depletion of HDL may provide clues to understand lipid insertion of HDL. CONCLUSIONS: These data provide important information for the understanding of the structure/maturation of plasma HDL. Moreover, they suggest a powerful method for directly visualizing the major apolipoproteins of plasma lipoproteins or the protein component of lipoprotein-like lipid-protein complexes.
背景与目的:血浆脂蛋白的主要载脂蛋白在脂蛋白的结构完整性和生理功能中起着至关重要的作用。高密度脂蛋白(HDL)的主要载脂蛋白载脂蛋白A-I(apoA-I)已相继建立了十多种结构模型。在这些模型中,apoA-I被认为是以环状形式组装的。然而,迄今为止,在生理条件下尚无直接证据。 方法:在此,利用原子力显微镜(AFM)原位观察apoA-I的组装情况,apoA-I是通过预先固定在功能化云母片上的血浆HDL脂质成分的耗尽而暴露出来的。 结果:首次通过AFM直接观察并定量测量了血浆HDL中apoA-I的环状粗结构和三种详细结构(分别为新月形、有间隙的“O”形和括号形结构),这些结构具有结合清道夫受体的能力。这三种详细结构可能代表了HDL脂质成分耗尽的不同程度。HDL脂质耗尽的数据可能为理解HDL的脂质插入提供线索。 结论:这些数据为理解血浆HDL的结构/成熟提供了重要信息。此外,它们还提示了一种直接可视化血浆脂蛋白主要载脂蛋白或类脂蛋白脂质-蛋白质复合物蛋白质成分的有力方法。
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