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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Definition of antigen specificity for antimitochondrial proteins detected by Western blotting using native mitochondrial proteins in primary biliary cirrhosis.
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Definition of antigen specificity for antimitochondrial proteins detected by Western blotting using native mitochondrial proteins in primary biliary cirrhosis.

机译:在原发性胆汁性肝硬化中使用天然线粒体蛋白通过蛋白质印迹法检测抗线粒体蛋白的抗原特异性。

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The major autoantigens to anti-mitochondrial antibody (AMA) in primary biliary cirrhosis (PBC) have previously been identified to be PDC-E2, BCOADC-E2, and OGDC-E2. However, analysis of these autoantigens to AMA cannot be examined using the two routine assays; immmunofluorescence and ELISA. Moreover, there are some problems in specificity and sensitivity in these routine assays. So, analysis with Western blotting using native mitochondrial protein as the antigen is required; it allows the identification of the molecular weights for the proteins which react with AMA in patients' sera. However, since the antigen-proteins used are not unified, molecular weights of AMA corresponding proteins vary among laboratories. In the present study, as the first step to help address this issue, we investigated the antigen specificity of protein bands detected by Western blotting using our in-house bovine and porcine heart mitochondrial proteins. Three major recombinant mitochondrial proteins were prepared. The antigen specificity was examined by the absorption tests preincubated with the three recombinant mitochondrial proteins. The molecular weights of developing our bovine and porcine heart mitochondrial proteins using SDS-PAGE were multiple protein bands including 74, 52, 50, and 43 kDa protein bands. Of them, the 74, 50, and 43 kDa protein bands were absorbed with preincubations of recombinant PDC-E2, BCOADC-E2, and OGDC-E2 protein, respectively. AMA specificity of these three major proteins with our Western blotting was confirmed.
机译:先前已确定原发性胆汁性肝硬化(PBC)中抗线粒体抗体(AMA)的主要自身抗原是PDC-E2,BCOADC-E2和OGDC-E2。但是,无法使用两种常规测定法检查对AMA的这些自身抗原的分析。免疫荧光和ELISA。此外,在这些常规测定中,在特异性和敏感性方面存在一些问题。因此,需要使用天然线粒体蛋白作为抗原进行蛋白质印迹分析。它可以确定与患者血清中与AMA反应的蛋白质的分子量。但是,由于所使用的抗原蛋白不是统一的,因此AMA对应蛋白的分子量在实验室之间会有所不同。在本研究中,作为帮助解决此问题的第一步,我们调查了使用我们内部的牛和猪心脏线粒体蛋白通过蛋白质印迹检测的蛋白条带的抗原特异性。制备了三种主要的重组线粒体蛋白。通过与三种重组线粒体蛋白预孵育的吸收测试来检查抗原特异性。使用SDS-PAGE开发牛和猪心脏线粒体蛋白的分子量是多个蛋白带,包括74、52、50和43 kDa蛋白带。其中,分别通过预孵育重组PDC-E2,BCOADC-E2和OGDC-E2蛋白吸收了74、50和43 kDa的蛋白带。通过我们的蛋白质印迹证实了这三种主要蛋白质的AMA特异性。

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