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DNA-酶相互作用中的水介导相关性。

Water-mediated correlations in DNA-enzyme interactions.

作者信息

Kurian P, Capolupo A, Craddock T J A, Vitiello G

机构信息

Quantum Biology Laboratory, National Human Genome Center and Department of Medicine, Howard University College of Medicine, Washington, DC 20059, USA.

Università degli Studi di Salerno and INFN Gruppo Collegato di Salerno, 84084 Fisciano (Salerno), Italy.

出版信息

Phys Lett A. 2018 Jan 5;382(1):33-43. doi: 10.1016/j.physleta.2017.10.038. Epub 2017 Oct 23.

Abstract

In this paper we consider dipole-mediated correlations between DNA and enzymes in the context of their water environment. Such correlations emerge from electric dipole-dipole interactions between aromatic ring structures in DNA and in enzymes. We show that there are matching collective modes between DNA and enzyme dipole fields, and that a dynamic time-averaged polarization vanishes in the water dipole field only if either DNA, enzyme, or both are absent from the sample. This persistent field may serve as the electromagnetic image that, in popular colloquialisms about DNA biochemistry, allows enzymes to "scan" or "read" the double helix. Topologically nontrivial configurations in the coherent ground state requiring clamplike enzyme behavior on the DNA may stem, ultimately, from spontaneously broken gauge symmetries.

摘要

在本文中,我们在DNA和酶的水环境背景下考虑偶极介导的它们之间的相关性。这种相关性源于DNA和酶中芳香环结构之间的电偶极 - 偶极相互作用。我们表明,DNA和酶偶极场之间存在匹配的集体模式,并且仅当样品中不存在DNA、酶或两者都不存在时,动态时间平均极化才会在水偶极场中消失。这个持续存在的场可能充当电磁图像,用关于DNA生物化学的通俗说法来讲,它使酶能够“扫描”或“读取”双螺旋。相干基态中的拓扑非平凡构型要求酶在DNA上表现出类似夹子的行为,这最终可能源于自发破缺的规范对称性。

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