Komiyama T, Oki T, Inui T
Biochim Biophys Acta. 1983 May 20;740(1):80-7. doi: 10.1016/0167-4781(83)90124-0.
The effects of various new anthracycline antibiotics on DNA and RNA synthesis were studied using DNA polymerase I (EC 2.7.7.7), RNA polymerase (EC 2.7.7.6) obtained from Escherichia coli and reverse transcriptase obtained from avian myeloblastosis virus. Aclacinomycin A, its analogues, baumycins A1 and A2, adriamycin and daunomycin showed potent inhibitory effects on these polymerases, with calf thymus DNA as template, with IC50 values of 10-30 microM. With poly(rA) x d(pT)10 as template for reverse transcriptase, aclacinomycin A and daunomycin showed IC50 values higher than 500 microM. Baumycins B1, B2, C1, and C2 showed high IC50 values on three polymerases. Addition of excess template DNA to the reaction mixture reversed the inhibitory effect of anthracyclines. Addition of calf thymus DNA to anthracyclines caused a bathochromic and hypochromic change in the visible spectrum. Apparent binding constant for aclacinomycin A, its analogues, and adriamycin were in the range of (1-2) X 10(6) M-1. Aclacinomycin A and adriamycin also bind to heat denatured DNA, but not strongly to yeast RNA. From these results, the structure-activity relationships of new anthracyclines on DNA binding and polymerase reactions are discussed.
使用从大肠杆菌中获得的DNA聚合酶I(EC 2.7.7.7)、RNA聚合酶(EC 2.7.7.6)以及从禽成髓细胞瘤病毒中获得的逆转录酶,研究了各种新型蒽环类抗生素对DNA和RNA合成的影响。阿克拉霉素A及其类似物、鲍霉素A1和A2、阿霉素和柔红霉素对这些聚合酶表现出强效抑制作用,以小牛胸腺DNA为模板时,IC50值为10 - 30微摩尔。以聚(rA)×d(pT)10为逆转录酶的模板时,阿克拉霉素A和柔红霉素的IC50值高于500微摩尔。鲍霉素B1、B2、C1和C2对三种聚合酶表现出高IC50值。向反应混合物中添加过量的模板DNA可逆转蒽环类药物的抑制作用。向蒽环类药物中添加小牛胸腺DNA会导致可见光谱出现红移和减色变化。阿克拉霉素A及其类似物以及阿霉素的表观结合常数在(1 - 2)×10⁶ M⁻¹范围内。阿克拉霉素A和阿霉素也与热变性DNA结合,但与酵母RNA结合不强。根据这些结果,讨论了新型蒽环类药物在DNA结合和聚合酶反应方面的构效关系。