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[猕猴的蛋白酶抑制剂系统。通过等电聚焦和家系分析鉴定等位基因]

[The protease inhibitor system of macaques. The identification of alleles using isoelectric focusing and family analysis].

作者信息

Samil'chuk E I

出版信息

Zh Obshch Biol. 1989 May-Jun;50(3):417-22.

PMID:2788967
Abstract

Five alpha-1-antitrypsin (alpha-1-AT) phenotypes have been revealed by isoelectrofocusing (IEF) in sera of 215 crab-eating macaques. Alpha-1-AT was monomorphic in sera of 250 Rhesus monkeys. A new allele of macaque Pi-system, designated as B' was postulated in addition to existing two (B and C) on the basis of IEF data. The above conclusion was supported by family analysis, based on 35 monkey birth cases. Alpha-1-AT phenotype frequencies were in agreement with Hardy-Weinberg equation both in wild and capture born crab-eating macaques. Alpha-1-AT was found to be microheterogeneous: several zones of the protein were revealed by IEF and Western blotting with anti human alpha-1-AT serum. The pregnancy caused a sharp increase of one band. This may lead to false identification of alpha-1-AT phenotypes, particularly when acid starch gel electrophoresis is used for alpha-1-AT identification. Such misinterpretation during alpha-1-AT phenotyping may explain the disagreement with Hardy-Weinberg equation described earlier for crab-eating macaques.

摘要

通过等电聚焦(IEF)法在215只食蟹猕猴的血清中发现了5种α-1-抗胰蛋白酶(α-1-AT)表型。在250只恒河猴的血清中,α-1-AT呈单态性。根据IEF数据,除了现有的两个等位基因(B和C)外,推测猕猴Pi系统存在一个新的等位基因,命名为B'。基于35例猴子出生病例的家系分析支持了上述结论。在野生和圈养出生的食蟹猕猴中,α-1-AT表型频率均符合哈迪-温伯格方程。发现α-1-AT具有微异质性:通过IEF和用抗人α-1-AT血清进行的蛋白质印迹法可显示该蛋白质的几个区带。怀孕导致其中一条带明显增加。这可能导致α-1-AT表型的错误鉴定,尤其是当使用酸性淀粉凝胶电泳进行α-1-AT鉴定时。在α-1-AT表型分析过程中的这种错误解读可能解释了早期报道的食蟹猕猴与哈迪-温伯格方程不一致的情况。

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