首页> 外文期刊>Journal of cell biology >Preparation of a gap junction fraction from uteri of pregnant rats: the 28-kD polypeptides of uterus, liver, and heart gap junctions are homologous.
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Preparation of a gap junction fraction from uteri of pregnant rats: the 28-kD polypeptides of uterus, liver, and heart gap junctions are homologous.

机译:从妊娠大鼠的子宫制备间隙连接部分:子宫,肝脏和心脏间隙连接的28个多肽是同源的。

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摘要

A procedure for the preparation of a gap junction fraction from the uteri of pregnant rats is described. The uterine gap junctions, when examined by electron microscopy of thin sections and in negatively stained preparations, were similar to gap junctions isolated from heart and liver. Major proteins of similar apparent molecular weight (Mr 28,000) were found in gap junction fractions isolated from the uterus, heart, and liver, and were shown to have highly homologous structures by two-dimensional mapping of their tryptic peptides. An Mr 10,000 polypeptide, previously deduced to be a proteolytic product of the Mr 28,000 polypeptide of rat liver (Nicholson, B. J., L. J. Takemoto, M. W. Hunkapiller, L. E. Hood, and J.-P. Revel, 1983, Cell, 32:967-978), was also studied and shown by chymotryptic mapping to be homologous in the uterine, heart, and liver gap junction fractions. An antibody raised in rabbits to a synthetic peptide corresponding to an amino-terminal sequence of the liver gap junction protein recognized Mr 28,000 proteins in the three tissues studied, showing that the proteins shared common antigenic determinants. These results indicate that gap junctions are biochemically conserved plasma membrane specializations. The view that gap junctions are tissue-specific plasma membrane organelles based on previous comparisons of Mr 26,000-30,000 polypeptides is not sustained by the present results.
机译:描述了从妊娠大鼠的子宫制备间隙连接部分的方法。当通过电子显微镜检查薄切片和阴性染色制剂时,子宫间隙连接类似于从心脏和肝脏分离的间隙连接。在从子宫,心脏和肝脏分离的间隙连接部分中发现了具有相似表观分子量(Mr 28,000)的主要蛋白质,并且通过对它们的胰蛋白酶解肽进行二维定位,显示出具有高度同源的结构。 10,000多肽,先前被推论为大鼠肝脏28,000多肽的蛋白水解产物(Nicholson,BJ,LJ Takemoto,MW Hunkapiller,LE Hood和J.-P. Revel,1983,Cell,32:967- 978),也经过了胰凝乳图谱的研究,显示在子宫,心脏和肝脏的间隙连接部分中是同源的。在兔体内针对对应于肝间隙连接蛋白氨基末端序列的合成肽产生的抗体识别了所研究的三个组织中的28,000个Mr蛋白质,表明该蛋白质具有共同的抗原决定簇。这些结果表明,间隙连接是生化保守的质膜特化。基于Mr 26,000-30,000多肽的先前比较,间隙连接是组织特异性质膜细胞器的观点不能被当前结果所支持。

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