Lanzillo J J, Fanburg B L
Biochemistry. 1977 Dec 13;16(25):5491-5. doi: 10.1021/bi00644a015.
The angiotensin I converting enzyme was purified 101 000-fold to homogeneity from human plasma by a combination of chromatographic and electrophoretic techniques. The enzyme is similar to other angiotensin I converting enzymes. It is an acidic glycoprotein consisting of a single polypeptide chain of molecular weight 140 000 with an isoelectric point of 4.6. The enzyme requires chloride ion for activity and is inhibited by ethylenediaminetetraacetic acid, angiotensin II, bradykinin, bradykinin potentiating factor nonapeptide, and 3-mercapto-2-D-methylpropanoyl-L-proline (SQ-14,225). The purified preparation cleaves bradykinin as well as angiotensin II and hippuryl-L-histidyl-L-leucine. Its specific activity with angiotensin I is 2.4 units per mg and with hippuryl-L-histidyl-L-leucine is 31.4 units per mg.
通过色谱和电泳技术相结合,从人血浆中纯化出血管紧张素I转换酶,纯化倍数达101000倍,达到同质。该酶与其他血管紧张素I转换酶相似。它是一种酸性糖蛋白,由一条分子量为140000的单多肽链组成,等电点为4.6。该酶的活性需要氯离子,并且受乙二胺四乙酸、血管紧张素II、缓激肽、缓激肽增强因子九肽和3-巯基-2-D-甲基丙酰-L-脯氨酸(SQ-14,225)抑制。纯化制剂可裂解缓激肽以及血管紧张素II和马尿酰-L-组氨酰-L-亮氨酸。其对血管紧张素I的比活性为每毫克2.4单位,对马尿酰-L-组氨酰-L-亮氨酸的比活性为每毫克31.4单位。