Structure and function of HDL mimetics.

Structure and function of HDL mimetics.
复制标题

DOI:
10.1161/atvbaha.109.187518
复制
发表时间:
2010-02
期刊:
Arteriosclerosis, thrombosis, and vascular biology
影响因子:
--
通讯作者:
Fogelman AM
Fogelman AM
中科院分区:
其他
文献类型:
--
作者:
Navab M;Shechter I;Anantharamaiah GM;Reddy ST;Van Lenten BJ;Fogelman AM

文献摘要

被引文献

相似文献

HDL模拟物已经由许多具有不同结构的肽和蛋白质构建,所有这些肽和蛋白质都结合HDL中发现的脂质。含有肽或蛋白质的HDL模拟物已被构建为具有少至4个和多至243个氨基酸残基。一些HDL模拟物已经用脂质但没有肽或蛋白质组分构建。一些HDL模拟物促进胆固醇流出,与人载脂蛋白A-I(apoA-I)相比,一些已被证明具有显著的结合氧化脂质的能力。许多这些肽已被证明具有抗炎特性。基于在许多动物模型和早期人类临床试验中的研究,HDL模拟物似乎有希望作为诊断和治疗剂。
HDL mimetics have been constructed from a number of peptides and proteins with varying structures, all of which bind lipids found in HDL. HDL mimetics containing a peptide or protein have been constructed with as few as 4 and as many as 243 amino acid residues. Some HDL mimetics have been constructed with lipid but without a peptide or protein component. Some HDL mimetics promote cholesterol efflux, some have been shown to have a remarkable ability to bind oxidized lipids compared to human apolipoprotein A-I (apoA-I). Many of these peptides have been shown to have anti-inflammatory properties. Based on studies in a number of animal models and in early human clinical trials, HDL mimetics appear to have promise as diagnostic and therapeutic agents.