University of Rome Tor Vergata, Department of Biology, Via Della Ricerca Scientifica, 00133 Rome, Italy.
Naxospharma srl, Via G. Di Vittorio, 70, 20026 Novate Milanese, Italy.
Int J Biol Macromol. 2015;77:68-75. doi: 10.1016/j.ijbiomac.2015.02.051. Epub 2015 Mar 14.
Topoisomerases IB are anticancer and antimicrobial targets whose inhibition by several natural and non-natural compounds has been documented. The inhibition effect by berberine and some 13-(di)phenylalkyl berberine derivatives has been tested towards human topoisomerase IB. Derivatives belonging to the 13-diphenylalkyl series display an efficient inhibition of the DNA relaxation and cleavage step, that increases upon pre-incubation with the enzyme. The religation step of the enzyme catalytic cycle is not affected by compounds and only slightly upon pre-incubation. The binding of the protein to the DNA substrate occurs also in the presence of the compounds, as monitored by a DNA shift assay, indicating that the compounds are not able to inhibit the formation of the enzyme-DNA complex but that they act as catalytic inhibitors.
拓扑异构酶 IB 是抗癌和抗微生物药物的靶点,其活性已被多种天然和非天然化合物所抑制。本研究测试了小檗碱和一些 13-(二)苯基烷基小檗碱衍生物对人拓扑异构酶 IB 的抑制作用。属于 13-(二)苯基烷基系列的衍生物对 DNA 松弛和切割步骤有高效的抑制作用,并且在与酶预孵育时增加。酶催化循环的连接步骤不受化合物影响,仅在预孵育时略有影响。通过 DNA 迁移实验监测到,化合物的存在不影响蛋白质与 DNA 底物的结合,表明化合物不能抑制酶-DNA 复合物的形成,而是作为催化抑制剂起作用。