Shennan K I, Smeekens S P, Steiner D F, Docherty K
Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, UK.
FEBS Lett. 1991 Jun 24;284(2):277-80. doi: 10.1016/0014-5793(91)80703-6.
A human insulinoma cDNA (PC2) that encodes a protein homologous to the Kex2/subtilisin-like proteinases has recently been described [1990, J. Biol. Chem. 265, 2997-3000]. In order to characterise the associated proteinase activity, mRNA encoding PC2 was synthesised in vitro and microinjected into Xenopus oocytes. The proteinase activity released into the media from oocytes microinjected with PC2 mRNA was assayed using small peptide fluorogenic substrates. Boc.Gln.Arg.Arg aminomethyl coumarin was hydrolysed in a Ca(2+)-dependent manner, but substrate analogues bearing a single basic aminoacid were not. The substrate specificity, inhibitor profile, and pH optimum of 5.5 were compatible with an involvement of PC2 in prohormone processing in mammalian cells.
最近已描述了一种编码与Kex2/枯草杆菌蛋白酶样蛋白酶同源蛋白的人胰岛素瘤cDNA(PC2)[1990,《生物化学杂志》265,2997 - 3000]。为了表征相关的蛋白酶活性,体外合成了编码PC2的mRNA并显微注射到非洲爪蟾卵母细胞中。使用小肽荧光底物测定从注射了PC2 mRNA的卵母细胞释放到培养基中的蛋白酶活性。Boc.Gln.Arg.Arg氨基甲基香豆素以Ca(2+)依赖的方式被水解,但带有单个碱性氨基酸的底物类似物则不会。底物特异性、抑制剂谱以及5.5的最适pH与PC2参与哺乳动物细胞中激素原加工过程是相符的。