Kukhanova M K, Kuznetsova E V, Kraevskiĭ A A, O'Hara B, Bekker J, Morin J, Gluzman Ia
American Cyanamid Company, New York.
Mol Biol (Mosk). 1994 May-Jun;28(3):530-41.
A systematic analysis of DNA polymerase of human herpes simplex type 1 virus, cytomegalovirus, and human type 2 adenovirus with the help of a broad set of modified substrates of these enzymes has been carried out. It revealed compounds capable of inhibiting the DNA synthesis catalyzed both by all three enzymes and DNA polymerase alpha from human placenta. Compounds have been found which effectively and specifically inhibit the DNA synthesis catalyzed by some of the abovementioned enzymes. It has been shown that the molecular mechanism of inhibition consists either in the termination of DNA elongation or in inhibition without incorporation into the growing DNA chain.
借助这些酶的一系列广泛的修饰底物,对人单纯疱疹病毒1型、巨细胞病毒和人2型腺病毒的DNA聚合酶进行了系统分析。结果揭示了能够抑制这三种酶以及人胎盘DNA聚合酶α催化的DNA合成的化合物。还发现了能有效且特异性抑制上述某些酶催化的DNA合成的化合物。结果表明,抑制的分子机制要么在于DNA延伸的终止,要么在于不掺入正在生长的DNA链中的抑制作用。