Smeekens S P
Chiron Corporation, Emeryville, CA 94608.
Biotechnology (N Y). 1993 Feb;11(2):182-6. doi: 10.1038/nbt0293-182.
The recent identification of a novel family of mammalian endoproteases that carry out intracellular processing of protein precursors at dibasic sites has ended a search that began twenty-five years ago with the discovery of the first such precursor, proinsulin. The five proteases found thus far are all related to the yeast dibasic-specific endoprotease kex2, and include PC2, PC3/PC1, PC4, furin/PACE, and PACE4. All are Ca(2+)-dependent serine proteases with catalytic domains organized similarly to the bacterial subtilisins. The emerging characteristics of these endoproteases, including their tissue-specific expression, subcellular localization, and cleavage site selectivity, indicates that members of this family arose during evolution to process a diverse group of functionally distinct precursors in a highly specific, compartmentalized and regulated fashion.
最近发现了一类新的哺乳动物内切蛋白酶家族,它们在双碱性位点对蛋白质前体进行细胞内加工,从而结束了始于25年前发现第一个此类前体——胰岛素原的探索。迄今为止发现的这五种蛋白酶都与酵母双碱性特异性内切蛋白酶kex2相关,包括PC2、PC3/PC1、PC4、弗林蛋白酶/PACE和PACE4。它们都是钙依赖性丝氨酸蛋白酶,其催化结构域的组织方式与细菌枯草杆菌蛋白酶相似。这些内切蛋白酶新出现的特性,包括它们的组织特异性表达、亚细胞定位和切割位点选择性,表明该家族成员在进化过程中产生,以高度特异性、分区化和受调控的方式加工一组功能各异的前体。