Suppr超能文献

低密度脂蛋白(LDL)、脂蛋白[a](Lp[a])以及还原型Lp[a]与抗载脂蛋白B单克隆抗体的相互作用。

Interaction of LDL, Lp[a], and reduced Lp[a] with monoclonal antibodies against apoB.

作者信息

Gries A, Fievet C, Marcovina S, Nimpf J, Wurm H, Mezdour H, Fruchart J C, Kostner G M

机构信息

Institute of Physiology, University of Graz, Austria.

出版信息

J Lipid Res. 1988 Jan;29(1):1-8.

PMID:2451704
Abstract

Five monoclonal antibodies (2A, 9A, 6B, L3, L7) produced in mice against human apolipoprotein B were investigated by competitive and inhibitive electroimmunoassay (EIA) for their reactivity with low density lipoprotein (LDL), lipoprotein[a] (Lp[a]), and reduced Lp[a]. All of the antibodies reacted with apoB of the different lipoproteins indicated by very similar slopes of the binding curves. None of them gave a positive reaction with apolipoprotein[a]. The amount of apoB required for 50% inhibition of antibody binding varied for the different antibodies and lipoproteins. Antibody 9A showed almost the same affinity for LDL, Lp[a], and reduced Lp[a]. Antibodies 2A and 6B bound about twofold better to LDL and reduced Lp[a] than to untreated Lp[a]. Antibodies L3 and L7 needed nearly threefold higher amounts of Lp[a]-apoB for 50% inhibition of antibody binding than of apoB of LDL and reduced Lp[a]. The amount of apoB required for 50% inhibition of antibody binding was somewhat higher in inhibitive assay than in competitive assay. We suggest that apo[a] covers certain epitopes of apoB in native Lp[a] leading to a reduced reaction with the monoclonal antibodies. However, it could also be that the binding of the [a]antigen to apoB via disulfide bridges causes profound conformational changes of the apoB region exposed to the surface.

摘要

研究了在小鼠体内产生的五种抗人载脂蛋白B单克隆抗体(2A、9A、6B、L3、L7),通过竞争性和抑制性电免疫分析(EIA)检测它们与低密度脂蛋白(LDL)、脂蛋白[a](Lp[a])和还原型Lp[a]的反应性。所有抗体与不同脂蛋白的载脂蛋白B反应,结合曲线斜率非常相似。它们均未与载脂蛋白[a]产生阳性反应。不同抗体和脂蛋白抑制50%抗体结合所需的载脂蛋白B量各不相同。抗体9A对LDL、Lp[a]和还原型Lp[a]表现出几乎相同的亲和力。抗体2A和6B与LDL和还原型Lp[a]的结合能力比对未处理的Lp[a]的结合能力高约两倍。抗体L3和L7抑制50%抗体结合所需的Lp[a]-载脂蛋白B量比LDL和还原型Lp[a]的载脂蛋白B量高近三倍。抑制分析中抑制50%抗体结合所需的载脂蛋白B量比竞争分析中的略高。我们认为,载脂蛋白[a]覆盖了天然Lp[a]中载脂蛋白B的某些表位,导致与单克隆抗体的反应性降低。然而,也可能是[a]抗原通过二硫键与载脂蛋白B的结合导致暴露于表面的载脂蛋白B区域发生深刻的构象变化。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验