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利用氮化硅纳米孔对肽进行分离和纯化的医学博士研究

MD Investigation on Separation and Purification of Peptides Utilizing Silicon Nitride Nanopores.

作者信息

Zhu Jinyang, Zhang Jilong, Zhang Pengyin, Zhang Hao, Wang Song

机构信息

Institute of Theoretical Chemistry, College of Chemistry, Jilin University, 2 Liutiao Road, Changchun 130023, P. R. China.

School of Life Sciences, Jilin University, 2699 Qianjin Street, Changchun 130012, China.

出版信息

J Phys Chem B. 2025 Jul 10;129(27):6871-6878. doi: 10.1021/acs.jpcb.5c02453. Epub 2025 Jun 26.

Abstract

Nanopore technology has emerged as a pivotal tool in biomolecular analysis owing to its high sensitivity, single-molecule resolution, and label-free detection capabilities. However, its application in peptide separation and purification has not been extensively explored. In this study, a novel peptide separation strategy using SiN nanopores was proposed for the separation of three peptides─VEGF, FGF, and EGF─by integrating conventional molecular dynamics simulation, steered molecular dynamics, and umbrella sampling approach. Our simulation results demonstrate that the three peptides traverse SiN nanopores with distinct energy barriers, indicating that the nanopores effectively differentiate between these similar peptides. This finding opens up possibilities for the separation of related peptides. Furthermore, we provide atomic-level insights into the underlying mechanisms responsible for the differences in translocation energy barriers among the peptides, thereby enriching the mechanistic understanding of peptide-nanopore interactions. Moreover, by analyzing the conformational dynamics of peptide translocation, we identify the crucial role of molecular sequence characteristics, such as length, polarity, hydrophobicity, and flexibility, in determining the peptide-nanopore interactions.

摘要

纳米孔技术因其高灵敏度、单分子分辨率和无标记检测能力,已成为生物分子分析中的关键工具。然而,其在肽分离和纯化中的应用尚未得到广泛探索。在本研究中,提出了一种使用氮化硅纳米孔的新型肽分离策略,通过整合传统分子动力学模拟、引导分子动力学和伞形采样方法,分离三种肽——血管内皮生长因子(VEGF)、成纤维细胞生长因子(FGF)和表皮生长因子(EGF)。我们的模拟结果表明,这三种肽穿过氮化硅纳米孔时具有不同的能垒,表明纳米孔能有效区分这些相似的肽。这一发现为相关肽的分离开辟了可能性。此外,我们提供了原子水平的见解,以了解肽之间转位能垒差异的潜在机制,从而丰富了对肽 - 纳米孔相互作用的机理理解。此外,通过分析肽转位的构象动力学,我们确定了分子序列特征(如长度、极性、疏水性和柔韧性)在决定肽 - 纳米孔相互作用中的关键作用。

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