Liu Zhiguo, Liu Ruisi, Zhou Zhen, Zu Yuangang, Xu Fengjie
State Engineering Laboratory of Bio-Resource Eco-Utilization, Harbin 150040, People's Republic of China; Engineering Research Center of Forest Bio-preparation, Ministry of Education, Northeast Forestry University, Harbin 150040, People's Republic of China; Key Laboratory of Forest Plant Ecology of Ministry of Education, Northeast Forestry University, Harbin 150040, People's Republic of China.
State Engineering Laboratory of Bio-Resource Eco-Utilization, Harbin 150040, People's Republic of China; Engineering Research Center of Forest Bio-preparation, Ministry of Education, Northeast Forestry University, Harbin 150040, People's Republic of China; Key Laboratory of Forest Plant Ecology of Ministry of Education, Northeast Forestry University, Harbin 150040, People's Republic of China.
Biochem Biophys Res Commun. 2015 Feb 20;457(4):688-92. doi: 10.1016/j.bbrc.2015.01.050. Epub 2015 Jan 22.
Interaction between long DNA molecules and activated cisplatin is believed to be crucial to anticancer activity. However, the exact structural changes of long DNA molecules induced by cisplatin are still not very clear. In this study, structural changes of long linear double-stranded DNA (dsDNA) and short single-stranded DNA (ssDNA) induced by activated cisplatin have been investigated by atomic force microscopy (AFM). The results indicated that long DNA molecules gradually formed network structures, beads-on-string structures and their large aggregates. Electrostatic and coordination interactions were considered as the main driving forces producing these novel structures. An interesting finding in this study is the beads-on-string structures. Moreover, it is worth noting that the beads-on-string structures were linked into the networks, which can be ascribed to the strong DNA-DNA interactions. This study expands our knowledge of the interactions between DNA molecules and cisplatin.
长链DNA分子与活化顺铂之间的相互作用被认为对抗癌活性至关重要。然而,顺铂诱导的长链DNA分子的确切结构变化仍不太清楚。在本研究中,通过原子力显微镜(AFM)研究了活化顺铂诱导的长线性双链DNA(dsDNA)和短单链DNA(ssDNA)的结构变化。结果表明,长链DNA分子逐渐形成网络结构、串珠状结构及其大聚集体。静电和配位相互作用被认为是产生这些新结构的主要驱动力。本研究中的一个有趣发现是串珠状结构。此外,值得注意的是,串珠状结构连接成网络,这可归因于强烈的DNA-DNA相互作用。本研究扩展了我们对DNA分子与顺铂之间相互作用的认识。