Radu A, Blobel G, Wozniak R W
Laboratory of Cell Biology, Rockefeller University, New York, New York 10021.
J Biol Chem. 1994 Jul 1;269(26):17600-5.
We have previously described procedures for the isolation of potential nuclear pore complex proteins (nucleoporins or Nups) from rat liver nuclear envelopes and their subsequent subfractionation into those binding to wheat germ agglutinin (WGA) and those that do not. One of these non-WGA-reactive proteins, termed Nup155, was previously molecularly cloned and sequenced and by immunoelectron microscopy shown to be a bona fide nucleoporin. Here we have characterized a second protein of the non-WGA-reactive type and show that it is a Nup as well. Molecular cloning and sequencing revealed that the protein has a calculated molecular mass of 107.2 kDa. It is, therefore, termed Nup107 (for nucleoporin of 107 kDa). Like other Nups that have so far been analyzed, Nup107 contains an abundance of kinase consensus sites. However, the primary structure of Nup107 is unique and not similar to other proteins in the data banks. Its most striking feature is a leucine zipper in its carboxyl-terminal region.
我们之前已经描述了从大鼠肝核被膜中分离潜在核孔复合体蛋白(核孔蛋白或Nups)的方法,以及随后将它们亚分级为与麦胚凝集素(WGA)结合的蛋白和不与WGA结合的蛋白的过程。这些非WGA反应性蛋白之一,称为Nup155,先前已进行分子克隆和测序,并通过免疫电子显微镜显示为真正的核孔蛋白。在这里,我们对第二种非WGA反应性类型的蛋白进行了表征,并表明它也是一种Nup。分子克隆和测序显示该蛋白的计算分子量为107.2 kDa。因此,它被称为Nup107(代表107 kDa的核孔蛋白)。与迄今为止分析过的其他Nups一样,Nup107含有大量的激酶共有位点。然而,Nup107的一级结构是独特的,与数据库中的其他蛋白不相似。其最显著的特征是在其羧基末端区域有一个亮氨酸拉链。