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解析细菌单链序列特异性:寡核苷酸探针的分子动力学和 MMPBSA 分析的见解。

Unraveling Bacterial Single-Stranded Sequence Specificities: Insights from Molecular Dynamics and MMPBSA Analysis of Oligonucleotide Probes.

机构信息

Division of Physical Science, Faculty of Science, Prince of Songkla University, Songkhla, 90110, Thailand.

Department of Chemistry, Center of Theoretical and Computational Physics, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.

出版信息

Mol Biotechnol. 2024 Apr;66(4):582-591. doi: 10.1007/s12033-024-01082-0. Epub 2024 Feb 19.

Abstract

We utilized molecular dynamics (MD) simulations and Molecular Mechanics Poisson-Boltzmann Surface Area (MMPBSA) free energy calculations to investigate the specificity of two oligonucleotide probes, namely probe B and probe D, in detecting single-stranded DNA (ssDNA) within three bacteria families: Enterobacteriaceae, Pasteurellaceae, and Vibrionaceae. Due to the limited understanding of molecular mechanisms in the previous research, we have extended the discussion to focus specifically on investigating the binding process of bacteria-probe DNA duplexes, with an emphasis on analyzing the binding free energy. The role of electrostatic contributions in the specificity between the oligonucleotide probes and the bacterial ssDNAs was investigated and found to be crucial. Our calculations yielded results that were highly consistent with the experimental data. Through our study, we have successfully exhibited the benefits of utilizing in-silico approaches as a powerful virtual-screening tool, particularly in research areas that demand a thorough comprehension of molecular interactions.

摘要

我们利用分子动力学(MD)模拟和分子力学泊松-玻尔兹曼表面面积(MMPBSA)自由能计算来研究两种寡核苷酸探针(探针 B 和探针 D)在检测三种细菌家族(肠杆菌科、巴斯德氏菌科和弧菌科)中的单链 DNA(ssDNA)时的特异性。由于之前的研究对分子机制的了解有限,我们将讨论扩展到专门研究细菌-探针 DNA 双链体的结合过程,重点分析结合自由能。我们研究了静电贡献在寡核苷酸探针与细菌 ssDNA 之间的特异性中的作用,发现其至关重要。我们的计算结果与实验数据高度一致。通过我们的研究,我们成功地展示了将计算机模拟方法作为一种强大的虚拟筛选工具的优势,特别是在需要深入理解分子相互作用的研究领域。

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