Wright G E
Department of Pharmacology and Molecular Toxicology, University of Massachusetts Medical School, Worcester 01655, USA.
Acta Biochim Pol. 1996;43(1):115-24.
The modified nucleotides, N2-(p-n-butylphenyl)dGTP and 2-(p-n-butylanilino) dATP and related compounds have been developed as inhibitor-probes of B family DNA polymerases. Synthetic approaches to these compounds are summarized. The nucleotides are potent, non-substrate inhibitors of DNA polymerase a. In contrast, they inhibit other members of the family with less potency but act as substrates for these enzymes. Modelling of the inhibitor: enzyme binding mechanism has been done based on the known structure of E. coli DNA polymerase I, and site-directed mutagenesis experiments to evaluate this mechanism are proposed.
修饰核苷酸N2 -(对正丁基苯基)dGTP和2 -(对正丁基苯胺基)dATP及相关化合物已被开发为B族DNA聚合酶的抑制剂探针。总结了这些化合物的合成方法。这些核苷酸是DNA聚合酶α的强效非底物抑制剂。相比之下,它们对该家族的其他成员抑制作用较弱,但却是这些酶的底物。基于大肠杆菌DNA聚合酶I的已知结构对抑制剂与酶的结合机制进行了建模,并提出了定点诱变实验以评估该机制。