连接蛋白 32 抗体的组织特异性交叉反应:中枢神经系统特有的问题和解决方案。

Q2 Biochemistry, Genetics and Molecular Biology
Stephanie L Fowler, Ashleigh C McLean, Steffany A L Bennett
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引用次数: 7

摘要

缝隙连接蛋白是由 21 个连接蛋白组成的高度同源家族。在本文中,作者描述了一种组织特异性技术假象,它使中枢神经系统中连接蛋白 32 蛋白表达的分析变得复杂。作者发现,在大脑而非肝脏中,八种常用抗体对交叉反应蛋白表现出较高的亲和力,从而掩盖了对 connexin32 的检测。交叉反应在蛋白质经过还原/变性条件下的 Western 印迹分析中很明显,但在免疫沉淀或免疫荧光应用中却不明显。通过生物信息学分析,并通过蔗糖梯度分馏和免疫印迹法检测连接蛋白无效突变小鼠的裂解物,作者发现交叉反应蛋白与连接蛋白 32 不存在于相同的细胞区室中,而且很可能不是连接蛋白家族的成员。提出这些发现的目的是帮助减少目前实验室验证中枢神经系统中连接蛋白 32 表达变化所花费的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue-specific cross-reactivity of connexin32 antibodies: problems and solutions unique to the central nervous system.

Gap junction proteins are a highly homologous family of 21 connexins. Here, the authors describe a tissue-specific technical artifact complicating analysis of connexin32 protein expression in the central nervous system. The authors show that in brain, but not liver, eight commonly employed antibodies exhibit a higher affinity for a cross-reactive protein that masks the detection of connexin32. Cross-reactivity is evident in Western blot analyses when proteins are subjected to reducing/denaturing conditions but not immunoprecipitation or immunofluorescent applications. Through bioinformatic analyses, tested by sucrose gradient fractionation and immunoblotting of lysates from connexin null-mutant mice, the authors show that the cross-reactive protein is not found in the same cellular compartments as connexin32 and is likely not a member of the connexin family. These findings are presented with the intent of helping to reduce the amount of time laboratories currently expend in validating changes in connexin32 expression in the central nervous system.

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来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
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