Kohanoff Jorge, McAllister Maeve, Tribello Gareth A, Gu Bin
Atomistic Simulation Centre, Queen's University Belfast, Belfast BT7 1NN, United Kingdom.
J Phys Condens Matter. 2017 Sep 27;29(38):383001. doi: 10.1088/1361-648X/aa79e3. Epub 2017 Jun 15.
DNA damage caused by irradiation has been studied for many decades. Such studies allow us to better assess the dangers posed by radiation, and to increase the efficiency of the radiotherapies that are used to combat cancer. A full description of the irradiation process involves multiple size and time scales. It starts with the interaction of radiation-either photons or swift ions-and the biological medium, which causes electronic excitation and ionisation. The two main products of ionising radiation are thus electrons and radicals. Both of these species can cause damage to biological molecules, in particular DNA. In the long run, this molecular level damage can prevent cells from replicating and can hence lead to cell death. For a long time it was assumed that the main actors in the damage process were the radicals. However, experiments in a seminal paper by the group of Leon Sanche in 2000 showed that low-energy electrons (LEE), such as those generated when ionising biological targets, can also cause bond breaks in biomolecules, and strand breaks in plasmid DNA in particular (Boudaiffa et al 2000 Science 287 1658-60). These results prompted a significant amount of experimental and theoretical work aimed at elucidating the role played by LEE in DNA damage. In this Topical Review we provide a general overview of the problem. We discuss experimental findings and theoretical results hand in hand with the aim of describing the physics and chemistry that occurs during the process of radiation damage, from the initial stages of electronic excitation, through the inelastic propagation of electrons in the medium, the interaction of electrons with DNA, and the chemical end-point effects on DNA. A very important aspect of this discussion is the consideration of a realistic, physiological environment. The role played by the aqueous solution and the amino acids from the histones in chromatin must be considered. Moreover, thermal fluctuations must be incorporated when studying these phenomena. Hence, a special place in this Topical Review is occupied by our recent first-principles molecular dynamics simulations that address the issue of how the environment favours or prevents LEEs from causing damage to DNA. We finish by summarising the conclusions achieved so far, and by suggesting a number of possible directions for further study.
几十年来,人们一直在研究辐射引起的DNA损伤。此类研究有助于我们更好地评估辐射带来的危险,并提高用于对抗癌症的放射疗法的效率。对辐射过程的完整描述涉及多个大小和时间尺度。它始于辐射(光子或快离子)与生物介质的相互作用,这会导致电子激发和电离。因此,电离辐射的两个主要产物是电子和自由基。这两种物质都会对生物分子造成损害,尤其是DNA。从长远来看,这种分子水平的损伤会阻止细胞复制,从而导致细胞死亡。长期以来,人们一直认为损伤过程中的主要因素是自由基。然而,2000年莱昂·桑切小组发表的一篇开创性论文中的实验表明,低能电子(LEE),比如在电离生物靶点时产生的那些电子,也会导致生物分子中的化学键断裂,尤其是质粒DNA中的链断裂(布代法等人,2000年,《科学》287卷,第1658 - 1660页)。这些结果引发了大量旨在阐明低能电子在DNA损伤中所起作用的实验和理论研究。在本专题综述中,我们对该问题进行了全面概述。我们将实验结果和理论结果结合起来讨论,目的是描述辐射损伤过程中发生的物理和化学过程,从电子激发的初始阶段,到电子在介质中的非弹性传播、电子与DNA的相互作用,以及对DNA的化学终点效应。本次讨论的一个非常重要的方面是考虑现实的生理环境。必须考虑水溶液和染色质中组蛋白氨基酸所起的作用。此外,在研究这些现象时必须纳入热涨落。因此,我们最近进行的第一性原理分子动力学模拟在本专题综述中占据了特殊地位,这些模拟解决了环境如何促进或阻止低能电子对DNA造成损伤的问题。我们通过总结目前已取得的结论,并提出一些可能的进一步研究方向来结束本文。