Yagura T, Kozu T, Seno T
J Biochem. 1981 Nov;90(5):1397-403. doi: 10.1093/oxfordjournals.jbchem.a133605.
The nature of the inhibitory effects of rifamycin derivative AF/013 (O-n-octyloxime of rifamycin SV) on DNA polymerases alpha and gamma were studied. Lineweaver-Burk analysis of the inhibition of DNA polymerases with respect to a substrate and template-primer showed a different mode of inhibition by AF/013 for each: the inhibition of DNA polymerase gamma was competitive with both dTTP and poly(rA)-oligo(dT), while that of DNA polymerase alpha was competitive with activated calf thymus DNA and non-competitive with dTTP. Further analysis of the competitive mode of the inhibition of DNA polymerase alpha, using poly(dT)-oligo(rA) as a template-primer, demonstrated that the primer molecule competed with AF/013. A change of effective divalent metal ion (Mn2+ in place of Mg2+) in the reaction mixture did not alter this competitive mode of inhibition with respect to the template-primer. The results of experiments to obtain further insight into the mechanism of drug-enzyme interaction suggest that AF/013 binds tightly to DNA polymerase alpha, and inhibits the process of chain elongation with DNA polymerases alpha and gamma.
研究了利福霉素衍生物AF/013(利福霉素SV的O-正辛基肟)对DNA聚合酶α和γ的抑制作用性质。针对底物以及模板引物对DNA聚合酶抑制作用的Lineweaver-Burk分析表明,AF/013对每种酶的抑制模式不同:AF/013对DNA聚合酶γ的抑制作用对dTTP和聚(rA)-寡聚(dT)均具有竞争性,而对DNA聚合酶α的抑制作用对活化的小牛胸腺DNA具有竞争性,对dTTP则为非竞争性。使用聚(dT)-寡聚(rA)作为模板引物对DNA聚合酶α抑制作用的竞争模式进行进一步分析,结果表明引物分子与AF/013存在竞争。反应混合物中有效二价金属离子的改变(用Mn2+代替Mg2+)并未改变针对模板引物的这种竞争性抑制模式。为进一步深入了解药物与酶相互作用机制而进行的实验结果表明,AF/013与DNA聚合酶α紧密结合,并抑制DNA聚合酶α和γ的链延伸过程。