Catanese J J, Kress L F
Molecular and Cellular Biology Department, Roswell Park Cancer Institute, Buffalo, New York 14263.
Biochemistry. 1992 Jan 21;31(2):410-8. doi: 10.1021/bi00117a015.
Fractionation of opossum (Didelphis virginiana) serum with (NH4)2SO4, followed by chromatography on DEAE-Sepharose, phenyl-Sepharose, and Mono Q HR 5/5, has resulted in the isolation in homogeneous condition of a metalloproteinase inhibitor designated oprin (opossum proteinase inhibitor). Oprin is a single-chain glycoprotein (26% carbohydrate) with an estimated Mr = 52,000, pI = 3.5, and E(1%/1 cm) = 11. Oprin inhibited snake venom metalloproteinases, but showed no activity on venom serine proteinases or on bacterial metalloproteinases. Incubation of Crotalus atrox alpha-proteinase (EC 3.4.24.1) with oprin, and analysis of the reaction products by chromatography on Mono Q HR 5/5 and by electrophoresis under nondenaturing conditions, indicated formation of an inactive enzyme/inhibitor complex. The complex dissociated during SDS/polyacrylamide gel electrophoresis. An opossum liver cDNA library was immunoscreened, and clones containing cDNA encoding for part of the open reading frame for oprin were isolated. The cDNA inserts contained nucleotide sequences corresponding to two internal amino acid sequences of oprin which had been separately determined by protein sequence analysis. Protein database screening using a 211 amino acid sequence deduced from one of the cDNA inserts showed no significant homology to known proteinase inhibitors. There was, however, a 36% identity with human alpha 1B-glycoprotein, a plasma protein of unknown function related to the immunoglobulin supergene family. In addition, the amino-terminal sequence of oprin showed 46% identity with human alpha 1B-glycoprotein in a 26 amino acid residue overlap.(ABSTRACT TRUNCATED AT 250 WORDS)
用硫酸铵((NH4)2SO4)对负鼠(弗吉尼亚负鼠,Didelphis virginiana)血清进行分级分离,随后在DEAE-琼脂糖、苯基琼脂糖和Mono Q HR 5/5上进行色谱分离,已在均一条件下分离出一种金属蛋白酶抑制剂,命名为oprin(负鼠蛋白酶抑制剂)。Oprin是一种单链糖蛋白(含26%碳水化合物),估计分子量为52,000,等电点为3.5,吸光系数(E(1%/1 cm))为11。Oprin能抑制蛇毒金属蛋白酶,但对毒液丝氨酸蛋白酶或细菌金属蛋白酶无活性。将矛头蝮蛇α-蛋白酶(EC 3.4.24.1)与oprin一起孵育,并通过在Mono Q HR 5/5上进行色谱分析以及在非变性条件下进行电泳来分析反应产物,结果表明形成了一种无活性的酶/抑制剂复合物。该复合物在SDS/聚丙烯酰胺凝胶电泳过程中解离。对负鼠肝脏cDNA文库进行免疫筛选,分离出了包含编码oprin部分开放阅读框的cDNA的克隆。cDNA插入片段包含与oprin的两个内部氨基酸序列相对应的核苷酸序列,这两个序列已通过蛋白质序列分析分别确定。使用从其中一个cDNA插入片段推导的211个氨基酸序列对蛋白质数据库进行筛选,结果显示与已知蛋白酶抑制剂无明显同源性。然而,与人类α1B-糖蛋白有36%的同一性,α1B-糖蛋白是一种与免疫球蛋白超基因家族相关的功能未知的血浆蛋白。此外,oprin的氨基末端序列在26个氨基酸残基重叠区域与人类α1B-糖蛋白有46%的同一性。(摘要截短于250词)