Howard Hughes Medical Institute, Cornell University, Ithaca, NY, USA.
Department of Physics and LASSP, Cornell University, Ithaca, NY, USA.
Nat Chem Biol. 2023 May;19(5):641-650. doi: 10.1038/s41589-022-01235-9. Epub 2023 Jan 30.
Etoposide is a broadly employed chemotherapeutic and eukaryotic topoisomerase II poison that stabilizes cleaved DNA intermediates to promote DNA breakage and cytotoxicity. How etoposide perturbs topoisomerase dynamics is not known. Here we investigated the action of etoposide on yeast topoisomerase II, human topoisomerase IIα and human topoisomerase IIβ using several sensitive single-molecule detection methods. Unexpectedly, we found that etoposide induces topoisomerase to trap DNA loops, compacting DNA and restructuring DNA topology. Loop trapping occurs after ATP hydrolysis but before strand ejection from the enzyme. Although etoposide decreases the innate stability of topoisomerase dimers, it increases the ability of the enzyme to act as a stable roadblock. Interestingly, the three topoisomerases show similar etoposide-mediated resistance to dimer separation and sliding along DNA but different abilities to compact DNA and chirally relax DNA supercoils. These data provide unique mechanistic insights into the functional consequences of etoposide on topoisomerase II dynamics.
依托泊苷是一种广泛应用的化疗药物和真核拓扑异构酶 II 抑制剂,它通过稳定断裂的 DNA 中间体来促进 DNA 断裂和细胞毒性。依托泊苷如何干扰拓扑异构酶动力学尚不清楚。在这里,我们使用几种敏感的单分子检测方法研究了依托泊苷对酵母拓扑异构酶 II、人拓扑异构酶 IIα 和人拓扑异构酶 IIβ 的作用。出乎意料的是,我们发现依托泊苷诱导拓扑异构酶捕获 DNA 环,使 DNA 紧缩并重塑 DNA 拓扑结构。环捕获发生在 ATP 水解之后但在酶从链上弹出之前。尽管依托泊苷降低了拓扑异构酶二聚体的固有稳定性,但它增加了酶作为稳定障碍的能力。有趣的是,这三种拓扑异构酶在依托泊苷介导的抵抗二聚体分离和沿 DNA 滑动方面表现出相似的特性,但在使 DNA 紧缩和手性松弛 DNA 超螺旋方面的能力不同。这些数据为依托泊苷对拓扑异构酶 II 动力学的功能后果提供了独特的机制见解。