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在改变的生理条件下,通过分子动力学模拟理解 A/T 缺失粘性末端的“四链 DNA 结”的自组装动力学。

Understanding the self-assembly dynamics of A/T absent 'four-way DNA junctions with sticky ends' at altered physiological conditions through molecular dynamics simulations.

机构信息

Department of Physics, Deen Dayal Upadhyaya Gorakhpur University, Gorakhpur, India.

Department of Physics, B.R.D. Post Graduate College, Deoria, India.

出版信息

PLoS One. 2023 Feb 8;18(2):e0278755. doi: 10.1371/journal.pone.0278755. eCollection 2023.

DOI:10.1371/journal.pone.0278755
PMID:36753480
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9907842/
Abstract

Elucidation of structure and dynamics of alternative higher-order structures of DNA such as in branched form could be targeted for therapeutics designing. Herein, we are reporting the intrinsically dynamic and folds transitions of an unusual DNA junction with sequence d(CGGCGGCCGC)4 which self-assembles into a four-way DNA junction form with sticky ends using long interval molecular simulations under various artificial physiological conditions. The original crystal structure coordinates (PDB ID: 3Q5C) for the selected DNA junction was considered for a total of 1.1 μs molecular dynamics simulation interval, including different temperature and pH, under OPLS-2005 force field using DESMOND suite. Following, post-dynamics structure parameters for the DNA junction were calculated and analyzed by comparison to the crystal structure. We show here that the self-assembly dynamics of DNA junction is mitigated by the temperature and pH sensitivities, and discloses peculiar structural properties as function of time. From this study it can be concluded on account of temperature sensitive and pH dependent behaviours, DNA junction periodic arrangements can willingly be synthesized and redeveloped for multiple uses like genetic biomarkers, DNA biosensor, DNA nanotechnology, DNA Zipper, etc. Furthermore, the pH dis-regulation behaviour may be used to trigger the functionality of DNA made drug-releasing nanomachines.

摘要

阐明 DNA 的替代高级结构(如分支形式)的结构和动力学可能是治疗设计的目标。在这里,我们报告了一种不寻常的 DNA 连接序列 d(CGGCGGCCGC)4 的固有动力学和折叠转变,该序列使用长间隔分子模拟在各种人工生理条件下自组装成带有粘性末端的四向 DNA 连接形式。所选 DNA 连接的原始晶体结构坐标(PDB ID:3Q5C)用于总共 1.1 μs 的分子动力学模拟间隔,包括不同的温度和 pH 值,在 OPLS-2005 力场下使用 DESMOND 套件。随后,通过与晶体结构进行比较,计算和分析 DNA 连接的后动力学结构参数。我们在这里表明,DNA 连接的自组装动力学受到温度和 pH 值敏感性的缓解,并揭示了作为时间函数的特殊结构特性。从这项研究中可以得出结论,由于温度敏感和 pH 值依赖性行为,DNA 连接的周期性排列可以自愿合成和重新开发,用于多种用途,如遗传生物标志物、DNA 生物传感器、DNA 纳米技术、DNA 拉链等。此外,pH 值失调行为可用于触发 DNA 制成的释药纳米机器的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b16/9907842/0974a4452808/pone.0278755.g014.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b16/9907842/0974a4452808/pone.0278755.g014.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b16/9907842/f5427827e32e/pone.0278755.g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b16/9907842/0974a4452808/pone.0278755.g014.jpg

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