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dsDNA 在铁磁体上吸附的自旋选择性损伤依赖性。

Spin Selectivity Damage Dependence of Adsorption of dsDNA on Ferromagnets.

机构信息

Department of Chemical and Biological Physics, Weizmann Institute, Rehovot 76100, Israel.

Chemistry Department, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.

出版信息

J Phys Chem B. 2023 Mar 23;127(11):2344-2350. doi: 10.1021/acs.jpcb.2c08820. Epub 2023 Mar 8.

Abstract

The adsorption of oxidatively damaged DNA onto ferromagnetic substrates was investigated. Both confocal fluorescence microscopy and quartz crystal microbalance methods show that the adsorption rate and the coverage depend on the magnetization direction of the substrate and the position of the damage site on the DNA relative to the substrate. SQUID magnetometry measurements show that the subsequent magnetic susceptibility of the DNA-coated ferromagnetic film depends on the direction of the magnetic field that was applied to the ferromagnetic film as the molecules were adsorbed. This study reveals that (i) the spin and charge polarization in DNA molecules is changed significantly by oxidative damage in the G bases and (ii) the rate of adsorption on a ferromagnet, as a function of the direction of the magnetic dipole of the surface, can be used as an assay to detect oxidative damage in the DNA.

摘要

研究了氧化性损伤 DNA 在铁磁基底上的吸附。共聚焦荧光显微镜和石英晶体微天平方法都表明,吸附速率和覆盖率取决于基底的磁化方向以及 DNA 上损伤部位相对于基底的位置。超导量子干涉磁力计测量表明,随后 DNA 包裹的铁磁膜的磁敏性取决于将分子吸附时施加到铁磁膜上的磁场的方向。这项研究揭示了:(i)在 G 碱基中,DNA 分子的自旋和电荷极化因氧化损伤而发生显著变化;(ii)作为一种探测 DNA 氧化损伤的方法,可以根据表面磁偶极子的方向来检测铁磁体上的吸附速率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aba/10041612/5b1d4febc8d1/jp2c08820_0002.jpg

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