| Literature DB >> 33570402 |
Ke Lu1,2, Cuifang Liu3, Yinuo Liu1, Anfeng Luo4, Jun Chen4, Zhichao Lei5, Jingwei Kong1,2, Xue Xiao1,2, Shuming Zhang1,6, Yi-Zhou Wang7, Lu Ma1, Shuo-Xing Dou1,2, Peng-Ye Wang1,2,8, Ming Li1,2,8, Guohong Li3,2, Wei Li1,8, Ping Chen4,3.
Abstract
The candidate anticancer drug curaxins can insert into DNA base pairs and efficiently inhibit the growth of various cancers. However, how curaxins alter the genomic DNA structure and affect the DNA binding property of key proteins remains to be clarified. Here, we first showed that curaxin CBL0137 strongly stabilizes the interaction between the double strands of DNA and reduces DNA bending and twist rigidity simultaneously, by single-molecule magnetic tweezers. More importantly, we found that CBL0137 greatly impairs the binding of CTCF but facilitates trapping FACT on DNA. We revealed that CBL0137 clamps the DNA double helix that may induce a huge barrier for DNA unzipping during replication and transcription and causes the distinct binding response of CTCF and FACT on DNA. Our work provides a novel mechanical insight into CBL0137's anticancer mechanisms at the nucleic acid level.Entities:
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Year: 2021 PMID: 33570402 DOI: 10.1021/acs.biochem.1c00014
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162