Kolpashchikov D M, Aleksandrova L A, Zakirova N F, Khodyreva S N, Lavrik O I
Novosibirsk Institute of Bioorganic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, Russia.
Bioorg Khim. 2000 Feb;26(2):151-5.
A new reagent for photoaffinity modification of biopolymers, 5-[E-N-(2-nitro-5-azidobenzoyl)-3-amino-1-propen-1-yl]-2',3'-dideoxyuridine 5'-triphosphate (NAB-ddUTP), was synthesized. Like a similar derivative of 2'-deoxyuridine 5'-triphosphate (NAB-dUTP), it was shown to be able to effectively substitute for dTTP in the synthesis of DNA catalyzed by eukaryotic DNA polymerase beta and to terminate DNA synthesis. A 5'-32P-labeled primer with a photoreactive group at the 3'-terminus was derived from NAB-ddUTP and used for photoaffinity labeling of the human replication protein A (RPA). The covalent attachment of RPA p32 and p70 subunits to the labeled primers was demonstrated. NAB-ddUTP is a promising tool for studying the interaction of proteins of the replicative complex with NA in cellular extracts and living cells during the termination of DNA synthesis.
合成了一种用于生物聚合物光亲和修饰的新试剂,即5-[E-N-(2-硝基-5-叠氮苯甲酰基)-3-氨基-1-丙烯-1-基]-2',3'-二脱氧尿苷5'-三磷酸(NAB-ddUTP)。与2'-脱氧尿苷5'-三磷酸(NAB-dUTP)的类似衍生物一样,它能够在真核DNA聚合酶β催化的DNA合成中有效替代dTTP并终止DNA合成。由NAB-ddUTP衍生出一种在3'-末端带有光反应基团的5'-32P标记引物,并用于人复制蛋白A(RPA)的光亲和标记。证实了RPA p32和p70亚基与标记引物的共价连接。NAB-ddUTP是研究DNA合成终止期间细胞提取物和活细胞中复制复合物蛋白与核酸相互作用的一种有前景的工具。