A T5 Exonuclease-Based Assay for DNA Topoisomerases and DNA Intercalators

被引:5
作者
Deng, Zifang [1 ,2 ]
Leng, Fenfei [1 ,2 ]
机构
[1] Florida Int Univ, Biomol Sci Inst, Miami, FL 33199 USA
[2] Florida Int Univ, Dept Chem & Biochem, Miami, FL 33199 USA
关键词
COLI CHROMOSOMAL ORIGIN; REPLICATION INITIATION; CATALYTIC PARAMETERS; ENDONUCLEASE; PURIFICATION; INHIBITORS; BINDING; GYRASE; MECHANISMS; CHEMISTRY;
D O I
10.1021/acsomega.1c00962
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA topoisomerases, essential enzymes to all living organisms, are important targets of certain antibiotics and anticancer drugs. Although efforts have been taken to identify new inhibitors targeting DNA topoisomerases, limited high throughput screening (HTS) studies have been conducted since a widely accessible HTS assay is not available. We report here the establishment of a fluorescence-based, low-cost HTS assay to identify topoisomerase inhibitors. This HTS assay is based on a unique property of T5 exonuclease that can completely digest supercoiled plasmid pAB1 containing an "AT" hairpin structure and spare relaxed pAB1 and has been validated by screening a small library that contains 50 compounds for various topoisomerases. This T5 exonuclease-based HTS assay can also be used to identify DNA intercalators, the major false positives for identifying topoisomerase inhibitors using this HTS assay. Additionally, we found a new compound that potently inhibits human and bacterial DNA topoisomerase I.
引用
收藏
页码:12205 / 12212
页数:8
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