Hu Zhihua, Deng Zun-Yi, Feng Hong-Jian
School of Physics, Northwest University, Xi'an 710127, China.
Phys Chem Chem Phys. 2024 Oct 9;26(39):25363-25372. doi: 10.1039/d4cp01917b.
The interaction between DNA and small molecules is important for understanding the mechanisms of DNA-based multifunctional devices and has been extensively studied. However, there are few reports on such interactions in irradiation environments. Here, we investigate the nonadiabatic dynamic behaviors of excited electrons in double-stranded DNA bound to BPQ molecule upon proton irradiation, focusing on the energy deposition and electronic excitation dynamics as protons traverse the DNA along different channels. Our results reveal that the presence of BPQ significantly influences charge migration and DNA damage, with notable differences between CGvdW and CGcovalent adducts. The energy deposition process is highly dependent on charge density, and guanine exhibits higher excitation propensity than cytosine due to its structural characteristics. The BPQ molecule enhances DNA charge migration and promotes damage through secondary electron migration. These findings provide insights into the nonadiabatic dynamics of DNA under ionizing radiation and have implications for designing targeted electrophilic organics to improve radiotherapy efficacy.
DNA与小分子之间的相互作用对于理解基于DNA的多功能器件的机制非常重要,并且已经得到了广泛研究。然而,关于辐照环境中此类相互作用的报道很少。在这里,我们研究了质子辐照下与BPQ分子结合的双链DNA中激发电子的非绝热动力学行为,重点关注质子沿不同通道穿过DNA时的能量沉积和电子激发动力学。我们的结果表明,BPQ的存在显著影响电荷迁移和DNA损伤,CGvdW和CG共价加合物之间存在显著差异。能量沉积过程高度依赖于电荷密度,由于鸟嘌呤的结构特征,其表现出比胞嘧啶更高的激发倾向。BPQ分子增强了DNA电荷迁移,并通过二次电子迁移促进损伤。这些发现为电离辐射下DNA的非绝热动力学提供了见解,并对设计靶向亲电有机物以提高放射治疗效果具有启示意义。