Hospattankar A V, Fairwell T, Appella E, Meng M, Brewer H B
Molecular Disease Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland 20892.
Biochem Biophys Res Commun. 1987 Nov 30;149(1):289-96. doi: 10.1016/0006-291x(87)91637-8.
In human plasma, apolipoprotein A-I is present as pro and mature isoproteins. The development of a highly specific antibody to the pro isoprotein of apoA-I has been difficult due to the close structural similarity between the pro and mature isoforms of apoA-I. To sermount this difficulty, a peptide was synthesized by the solid phase method which corresponded to the amino acid sequence present in the pro region of apoA-I. The synthetic peptide was coupled to serum albumin and the conjugate utilized to immunize rabbits for antibody production. Immunoblot analysis of purified proapoA-I and mature apoA-I revealed that the antibody was specific for the propeptide of apoA-I. Analysis of apoA-I in the plasma from a Tangier disease patient and newly secreted apoA-I from HepG2 cells clearly demonstrated the isoforms which contained the proisoprotein. The proapoA-I specific antibody should prove to be a useful tool in developing a radioimmunoassay for quantitation of the proisoprotein in plasma, isolation of proapoA-I from normal and dyslipoproteinemic subjects by immunoaffinity chromatography and in studies related to the synthesis and processing of apoA-I.
在人血浆中,载脂蛋白A-I以前体和成熟同种型存在。由于载脂蛋白A-I的前体和成熟同种型之间结构相似性高,因此很难开发出针对载脂蛋白A-I前体同种型的高特异性抗体。为克服这一困难,通过固相法合成了一种与载脂蛋白A-I前体区域中存在的氨基酸序列相对应的肽。将合成肽与血清白蛋白偶联,并利用该偶联物免疫兔子以产生抗体。对纯化的前载脂蛋白A-I和成熟载脂蛋白A-I进行免疫印迹分析表明,该抗体对载脂蛋白A-I的前肽具有特异性。对丹吉尔病患者血浆中的载脂蛋白A-I和来自HepG2细胞新分泌的载脂蛋白A-I进行分析,清楚地证明了含有前体同种型的同种型。载脂蛋白A-I特异性抗体应被证明是开发用于定量血浆中前体同种型的放射免疫测定、通过免疫亲和色谱从正常和血脂异常受试者中分离前载脂蛋白A-I以及与载脂蛋白A-I的合成和加工相关研究的有用工具。