Mitina R L, Mustaev A A, Zaychikov E F, Khomov V V, Lavrik O I
Novosibirsk Institute of Bioorganic Chemistry, Siberian Division, Academy of Sciences, USSR.
FEBS Lett. 1990 Oct 15;272(1-2):181-3. doi: 10.1016/0014-5793(90)80478-2.
Highly selective affinity labeling of the primer site of E. coli DNA polymerase I was performed with the 5'-reactive derivatives of oligothymidylate in the presence of poly(dA) template. Subtilysine cleavage proved that the site of affinity modification belonged to the 'Klenow' part of DNA polymerase I. If taken separately, Klenow fragment was not labeled by these oligonucleotide derivatives. The site of affinity labeling were tested in the structure of DNA polymerase I by hydroxylamine cleavage. At least two sites of labeling were revealed. The main one was localized between Gly-833 and His-928.
在聚(dA)模板存在的情况下,用寡聚胸苷酸的5'-反应性衍生物对大肠杆菌DNA聚合酶I的引物位点进行了高选择性亲和标记。枯草杆菌蛋白酶切割证明,亲和修饰位点属于DNA聚合酶I的“Klenow”部分。单独来看,Klenow片段不会被这些寡核苷酸衍生物标记。通过羟胺切割在DNA聚合酶I的结构中测试了亲和标记位点。发现了至少两个标记位点。主要位点位于甘氨酸-833和组氨酸-928之间。