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13-(二)苯基烷基小檗碱衍生物在调节人拓扑异构酶 IB 活性中的作用。

Role of 13-(di)phenylalkyl berberine derivatives in the modulation of the activity of human topoisomerase IB.

机构信息

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.

出版信息

Int J Biol Macromol. 2015;77:68-75. doi: 10.1016/j.ijbiomac.2015.02.051. Epub 2015 Mar 14.

Abstract

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.

摘要

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。

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