化学
加合物
奥沙利铂
纳米孔
DNA
组合化学
计算生物学
DNA测序器
生物物理学
DNA测序
生物化学
纳米技术
遗传学
有机化学
癌症
生物
材料科学
结直肠癌
作者
Ting Li,Wei Lü,Hui Tian,Yu Cao,Qianqian He,Xia Chen,Hailong Wang
标识
DOI:10.1021/acs.analchem.3c00461
摘要
The antitumor effect of Pt-based drugs is determined by their binding activity with deoxyribonucleic acid (DNA), and understanding the reaction process in a systematic manner is crucial. However, existing assays used for DNA–Pt research suffer from several issues, such as complicated sample preparation, preamplification, and expensive instruments, which dramatically limit their practical application. In this study, a novel method was presented to investigate the adducts of DNA and oxaliplatin using an α-hemolysin nanopore sensor. This approach allows for real-time monitoring of the DNA–oxaliplatin condensation process through the detection of nanopore events associated with DNA–oxaliplatin adducts. Specifically, type I and II signals exhibiting specific current characteristics were observed during the process. Typical signals with high frequency were obtained by recording the designed DNA sequence. Furthermore, the production of these signals was confirmed to be independent of homologous adducts. This finding suggests that the DNA–oxaliplatin adduct can serve as a potential sensor for detecting oxaliplatin lesions and multiple types of molecules.
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