Tanuma S, Kawashima K, Endo H
Biochem Biophys Res Commun. 1986 Mar 28;135(3):979-86. doi: 10.1016/0006-291x(86)91024-7.
HeLa S3 cells contained two activities (form I and II) that degrade (ADP-ribose)n exo-glycosidically. Form I was extracted from nuclei only by sonication in high ionic strength, while form II was soluble in cytosol. The two active forms differed in chromatographic behaviors, in their Km values for (ADP-ribose)n, and in their pH and salt requirements for optimal activity, although both forms exhibited properties characteristic of (ADP-ribose)n glycohydrolase such as requirement of sulfhydryl compounds and sensitivity of ADP-ribose and cAMP. Form I and II had apparent molecular weights of 72,000 and 53,000, respectively, as determined by gel filtration on Sepharose CL-6B.
海拉S3细胞含有两种外切糖苷酶活性(形式I和形式II),可降解聚(ADP-核糖)。形式I仅在高离子强度下通过超声处理从细胞核中提取,而形式II可溶于细胞质溶胶。这两种活性形式在色谱行为、对聚(ADP-核糖)的Km值以及最佳活性所需的pH和盐浓度方面存在差异,尽管两种形式都表现出聚(ADP-核糖)糖水解酶的特性,如对巯基化合物的需求以及对ADP-核糖和cAMP的敏感性。通过在琼脂糖CL-6B上进行凝胶过滤测定,形式I和形式II的表观分子量分别为72,000和53,000。