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通过去污剂扰动对人血浆脂蛋白进行重塑。

Remodeling of human plasma lipoproteins by detergent perturbation.

作者信息

Pownall Henry J

机构信息

Department of Medicine, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.

出版信息

Biochemistry. 2005 Jul 19;44(28):9714-22. doi: 10.1021/bi050729q.

Abstract

Detergent perturbation, the treatment of total human plasma lipoproteins (TLP) with sodium cholate and its subsequent removal, has been used to study lipoprotein dynamics and stability. At physiological TLP concentrations, detergent perturbation converts low-density lipoproteins (LDL) and high-density lipoproteins (HDL) to higher-particle weight species with the concomitant release of apo A-I but not apo A-II as a lipid-poor species. Detergent perturbation of isolated HDL also releases lipid-poor apo A-I and forms larger HDL species, whereas detergent perturbation of an isolated LDL has no effect on its size. A model is presented in which detergent perturbation induces transfer of PC from metastable HDL and LDL to mixed micelles with sodium cholate. The remaining LDL and HDL are unstable because of the loss of their surface components, phospholipid and/or apo A-I, and fuse to give larger LDL and HDL particles. These effects on HDL, i.e., PC transfer, apo A-I dissociation, and particle fusion, emulate the activity of human plasma phospholipid transfer protein. Thus, detergent perturbation is a new and potentially powerful method for determining lipoprotein stability, studying the mechanisms for remodeling of plasma lipoproteins, and preparing new forms of HDL and LDL with unique interactions with lipoprotein transporters and receptors.

摘要

去污剂扰动,即用人胆酸钠处理人血浆总脂蛋白(TLP)并随后去除该去污剂,已被用于研究脂蛋白的动力学和稳定性。在生理TLP浓度下,去污剂扰动将低密度脂蛋白(LDL)和高密度脂蛋白(HDL)转变为更高分子量的物种,同时释放出脂质含量低的载脂蛋白A-I,但不释放载脂蛋白A-II。对分离的HDL进行去污剂扰动也会释放脂质含量低的载脂蛋白A-I并形成更大的HDL物种,而对分离的LDL进行去污剂扰动对其大小没有影响。本文提出了一个模型,其中去污剂扰动诱导磷脂酰胆碱(PC)从亚稳态的HDL和LDL转移到与人胆酸钠形成的混合胶束中。剩余的LDL和HDL由于其表面成分(磷脂和/或载脂蛋白A-I)的丢失而不稳定,并融合形成更大的LDL和HDL颗粒。这些对HDL的影响,即PC转移、载脂蛋白A-I解离和颗粒融合,模拟了人血浆磷脂转移蛋白的活性。因此,去污剂扰动是一种新的且可能强大的方法,用于确定脂蛋白稳定性、研究血浆脂蛋白重塑机制以及制备与脂蛋白转运蛋白和受体具有独特相互作用的新型HDL和LDL。

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