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通过等电聚焦法显示的人血清β2-糖蛋白I的基因变异

Genetic variations of human serum beta 2-glycoprotein I demonstrated by isoelectric focusing.

作者信息

Richter A, Cleve H

机构信息

Institute of Anthropoloy and Human Genetics, University of Munich, Federal Republic of Germany.

出版信息

Electrophoresis. 1988 Jul;9(7):317-22. doi: 10.1002/elps.1150090706.

Abstract

Human serum beta 2-glycoprotein I was analyzed by isoelectric focusing followed by immunoprinting or immunoblotting with monospecific antiserum. Isoelectric focusing revealed a heterogeneous pattern consisting of 4 major and 4-5 minor bands with isoelectric points of the major bands between pH 5.4 and 6.2. Comparative analysis of sera from more than 400 healthy blood donors showed individual variations of band patterns: six different phenotypes were observed. A family study of 44 families with a total of 129 children demonstrated the genetic control of this variation. Presumably, three alleles, called B2G1, B2G2, and B2G*3, determine six phenotypes: B2G 1, 2, 3, 1-2, 1-3 and 2-3. The phenotype 3, however, has not been found in this study. An additional phenotype, noted in one serum specimen, was tentatively classified as B2G 2-4. The distribution of phenotypes and alleles in two populations, from Munich and from Tyrol, has been examined and the frequencies are presented. This genetic polymorphism appears not to be associated with inherited quantitative variations of beta 2-glycoprotein I found earlier. The inherited variations can still be recognized after treatment of sera with neuraminidase and with endoglycosidase F, although the banding pattern is altered and shifted towards the cathode. The genetic polymorphism can, therefore, not be ascribed to variations residing in the carbohydrate side chains.

摘要

采用等电聚焦,随后用单特异性抗血清进行免疫印记或免疫印迹法分析人血清β2-糖蛋白I。等电聚焦显示出一种异质性模式,由4条主要条带和4 - 5条次要条带组成,主要条带的等电点在pH 5.4至6.2之间。对400多名健康献血者的血清进行比较分析,结果显示条带模式存在个体差异:观察到六种不同的表型。对44个家庭共129名儿童进行的家系研究证明了这种变异受遗传控制。推测三个等位基因,即B2G1、B2G2和B2G*3,决定了六种表型:B2G 1、2、3、1 - 2、1 - 3和2 - 3。然而,在本研究中未发现表型3。在一份血清标本中发现的另一种表型,暂归类为B2G 2 - 4。已检测了来自慕尼黑和蒂罗尔的两个人群中表型和等位基因的分布,并列出了频率。这种遗传多态性似乎与早期发现的β2-糖蛋白I的遗传定量变异无关。用神经氨酸酶和内切糖苷酶F处理血清后,尽管条带模式发生改变并向阴极移动,但仍可识别出遗传变异。因此,遗传多态性不能归因于碳水化合物侧链中的变异。

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