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DNA 三联体中的短程电荷转移:相干涨落电子转移的实时追踪。

Short-Range Charge Transfer in DNA Base Triplets: Real-Time Tracking of Coherent Fluctuation Electron Transfer.

机构信息

Institute of Atomic and Molecular Physics, Jilin University, Changchun 130012, China.

出版信息

Molecules. 2023 Sep 25;28(19):6802. doi: 10.3390/molecules28196802.

Abstract

The short-range charge transfer of DNA base triplets has wide application prospects in bioelectronic devices for identifying DNA bases and clinical diagnostics, and the key to its development is to understand the mechanisms of short-range electron dynamics. However, tracing how electrons are transferred during the short-range charge transfer of DNA base triplets remains a great challenge. Here, by means of ab initio molecular dynamics and Ehrenfest dynamics, the nuclear-electron interaction in the thymine-adenine-thymine (TAT) charge transfer process is successfully simulated. The results show that the electron transfer of TAT has an oscillating phenomenon with a period of 10 fs. The charge density difference proves that the charge transfer proportion is as high as 59.817% at 50 fs. The peak position of the hydrogen bond fluctuates regularly between -0.040 and -0.056. The time-dependent Marcus-Levich-Jortner theory proves that the vibrational coupling between nucleus and electron induces coherent electron transfer in TAT. This work provides a real-time demonstration of the short-range coherent electron transfer of DNA base triplets and establishes a theoretical basis for the design and development of novel biological probe molecules.

摘要

DNA 三联体的短程电荷转移在用于识别 DNA 碱基和临床诊断的生物电子器件中有广泛的应用前景,其发展的关键是了解短程电子动力学的机制。然而,追踪 DNA 三联体的短程电荷转移过程中电子是如何转移的仍然是一个巨大的挑战。在这里,通过从头算分子动力学和 Ehrenfest 动力学,成功地模拟了胸腺嘧啶-腺嘌呤-胸腺嘧啶(TAT)电荷转移过程中的核-电子相互作用。结果表明,TAT 的电子转移具有 10 fs 的振荡现象。电荷密度差证明,在 50 fs 时,电荷转移比例高达 59.817%。氢键的峰值位置在-0.040 到-0.056 之间有规律地波动。含时 Marcus-Levich-Jortner 理论证明,原子核和电子之间的振动耦合诱导了 TAT 中的相干电子转移。这项工作为 DNA 三联体的短程相干电子转移提供了实时演示,并为新型生物探针分子的设计和开发奠定了理论基础。

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