Figueiredo A F, Takii Y, Tsuji H, Kato K, Inagami T
Biochemistry. 1983 Nov 22;22(24):5476-81. doi: 10.1021/bi00293a004.
Renin and cathepsin D were purified by seven-step procedures involving five steps common to both enzymes. These common five steps were extraction of freeze-dried kidney powder in 30% methoxyethanol-water, diethylaminoethyl-cellulose (DEAE-cellulose) batch absorption and elution, pepstatin-aminohexyl-Sepharose chromatography, Sephadex G-100 chromatography, and DEAE-cellulose chromatography. The renin component was purified further by passage through an anti-rat spleen cathepsin D immunoglobulin G-Sepharose (IgG-Sepharose) column followed by carboxymethyl-Sephadex (CM-Sepharose) chromatography which separated two renin components. Cathepsin D activity obtained by the fifth step was purified by passage through an anti-rat kidney renin IgG-Sepharose column followed by DEAE-Sephacel chromatography which separated three cathepsin D components. The homogeneity of renin and cathepsin D preparations was demonstrated by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis. The two components of renins showed molecular weights of 42 000 and 36 000 by gel filtration and 38 000 and 36 000 by SDS gel electrophoresis, respectively. They showed isoelectric points of 5.35 and 5.65 by electrofocusing in 5% polyacrylamide gels. Their optimum pHs of enzyme activity were 6.5 as determined by using nephrectomized rat plasma as a substrate. Their specific angiotensin I (Ang I) generation activities were 158 and 146 micrograms of Ang I (microgram of protein)-1 h-1, respectively, which correspond to 1100 and 1020 Goldblatt units (mg of protein)-1 h-1. The three cathepsins showed molecular weights of 41 000, 43 000, and 41 000 by gel filtration and 46 000, 45 000, and 46 000 by SDS gel electrophoresis.(ABSTRACT TRUNCATED AT 250 WORDS)
肾素和组织蛋白酶D通过七步程序进行纯化,其中五步是两种酶共有的。这五步共有程序为:用30%甲氧基乙醇-水提取冻干肾粉、二乙氨基乙基纤维素(DEAE-纤维素)分批吸附和洗脱、胃蛋白酶抑制剂-氨基己基琼脂糖凝胶色谱法、葡聚糖凝胶G-100色谱法以及DEAE-纤维素色谱法。肾素组分通过抗大鼠脾脏组织蛋白酶D免疫球蛋白G-琼脂糖凝胶(IgG-琼脂糖凝胶)柱进一步纯化,随后进行羧甲基琼脂糖凝胶(CM-琼脂糖凝胶)色谱法,该方法分离出两种肾素组分。通过五步获得的组织蛋白酶D活性通过抗大鼠肾肾素IgG-琼脂糖凝胶柱进一步纯化,随后进行DEAE-琼脂糖凝胶色谱法,该方法分离出三种组织蛋白酶D组分。通过十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳证明了肾素和组织蛋白酶D制剂的均一性。通过凝胶过滤,两种肾素组分的分子量分别为42000和36000,通过SDS凝胶电泳分别为38000和36000。通过在5%聚丙烯酰胺凝胶中进行等电聚焦,它们的等电点分别为5.35和5.65。以切除肾脏的大鼠血浆为底物测定,它们酶活性的最适pH值为6.5。它们产生特异性血管紧张素I(Ang I)的活性分别为158和146微克Ang I(微克蛋白)-1小时-1,分别相当于1100和1020戈德布拉特单位(毫克蛋白)-1小时-1。通过凝胶过滤,三种组织蛋白酶的分子量分别为41000、43000和41000,通过SDS凝胶电泳分别为46000、45000和46000。(摘要截断于250字)