Johnson D, Travis J
J Biol Chem. 1978 Oct 25;253(20):7142-4.
An unadecapeptide, obtained by papain digestion of denatured human alpha-1-proteinase inhibitor (alpha-1-PI), has been isolated and sequenced. The structure of this fragment overlaps with the NH2-terminal sequence of modified inhibitor (alpha-1-PI) prepared from dissociated complexes of alpha-1-PI with trypsin, chymotrypsin, and elastase. Furthermore, structural homology with the reactive centers of proteinase inhibitors from other sources is readily detectable. Methionine has been found to occupy the apparent P1 position in alpha-1-PI and the potential inactivation of the inhibitor by oxidation of this critical residue may be important in obtaining a biochemical link with the development of lung disease.
通过木瓜蛋白酶消化变性的人α1-蛋白酶抑制剂(α1-PI)获得的一种十一肽已被分离并测序。该片段的结构与由α1-PI与胰蛋白酶、胰凝乳蛋白酶和弹性蛋白酶的解离复合物制备的修饰抑制剂(α1-PI)的NH2末端序列重叠。此外,与其他来源的蛋白酶抑制剂的反应中心的结构同源性很容易检测到。已发现甲硫氨酸在α1-PI中占据明显的P1位置,该关键残基的氧化可能导致抑制剂的潜在失活,这在获得与肺部疾病发展的生化联系方面可能很重要。