鸟嘌呤
碱基
化学
电离
飞秒
生物分子
光化学
水溶液
密度泛函理论
离子
波包
激进的
DNA
计算化学
原子物理学
物理化学
激光器
有机化学
光学
物理
核苷酸
生物化学
基因
作者
Christine Chun Hui Ling,Wei Xin Chan,Jing Xuan Siow,Zhi-Heng Loh
标识
DOI:10.1021/acs.jpca.3c08232
摘要
Studying the ultrafast dynamics of ionized aqueous biomolecules is important for gaining an understanding of the interaction of ionizing radiation with biological matter. Guanine plays an essential role in biological systems as one of the four nucleobases that form the building blocks of deoxyribonucleic acid (DNA). Guanine radicals can induce oxidative damage to DNA, particularly due to the lower ionization potential of guanine compared to the other nucleobases, sugars, and phosphate groups that are constituents of DNA. This study utilizes femtosecond optical pump–probe spectroscopy to observe the ultrafast vibrational wave packet dynamics of the guanine radical anion launched by photodetachment of the aqueous guanine dianion. The vibrational wave packet motion is resolved into 11 vibrational modes along which structural reorganization occurs upon photodetachment. These vibrational modes are assigned with the aid of density functional theory (DFT) calculations. Our work sheds light on the ultrafast vibrational dynamics following the ionization of nucleobases in an aqueous medium.
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