Pecularities of DNA binding to two-dimensional crystals of bacterial protein Dps from Escherichia coli based on molecular dynamics data
- 作者: Tereshkin E.V.1, Tereshkina К.B.1, Loiko N.G.2, Kovalenko V.V.1, Krupyanskii Y.F.1
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隶属关系:
- Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences
- Federal Research Centre “Fundamentals of Biotechnology” of the Russian Academy of Sciences
- 期: 卷 43, 编号 12 (2024)
- 页面: 84-94
- 栏目: Chemical physics of biological processes
- URL: https://archivog.com/0207-401X/article/view/684180
- DOI: https://doi.org/10.31857/S0207401X24120086
- ID: 684180
如何引用文章
详细
In this work, using coarse-grained molecular modeling methods, the interactions of DNA-binding protein from starved cells (Dps) of the bacterium Escherichia coli with DNA sections of various lengths and composition were investigated. The binding features in two-dimensional crystals of the Dps protein were studied. Using free energy search methods – thermodynamic integration and linear interaction energy – the most favorable conditions for the binding of DNA and Dps were determined.
作者简介
E. Tereshkin
Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: ramm@mail.ru
俄罗斯联邦, Moscow
К. Tereshkina
Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences
Email: ramm@mail.ru
俄罗斯联邦, Moscow
N. Loiko
Federal Research Centre “Fundamentals of Biotechnology” of the Russian Academy of Sciences
Email: ramm@mail.ru
俄罗斯联邦, Moscow
V. Kovalenko
Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences
Email: ramm@mail.ru
俄罗斯联邦, Moscow
Y. Krupyanskii
Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences
Email: ramm@mail.ru
俄罗斯联邦, Moscow
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