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乙酰化对从头全原子自组装模拟壳聚糖纳米纤维形成的影响。

Effect of Acetylation on the Nanofibril Formation of Chitosan from All-Atom De Novo Self-Assembly Simulations.

机构信息

Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, MD 21201, USA.

Institute for Bioscience and Biotechnology Research, University of Maryland, College Park, MD 20742, USA.

出版信息

Molecules. 2024 Jan 23;29(3):561. doi: 10.3390/molecules29030561.

Abstract

Chitosan-based materials have broad applications, from biotechnology to pharmaceutics. Recent experiments showed that the degree and pattern of acetylation along the chitosan chain modulate its biological and physicochemical properties; however, the molecular mechanism remains unknown. Here, we report, to the best of our knowledge, the first de novo all-atom molecular dynamics (MD) simulations to investigate chitosan's self-assembly process at different degrees and patterns of acetylation. Simulations revealed that 10 mer chitosan chains with 50% acetylation in either block or alternating patterns associate to form ordered nanofibrils comprised of mainly antiparallel chains in agreement with the fiber diffraction data of deacetylated chitosan. Surprisingly, regardless of the acetylation pattern, the same intermolecular hydrogen bonds mediate fibril sheet formation while water-mediated interactions stabilize sheet-sheet stacking. Moreover, acetylated units are involved in forming strong intermolecular hydrogen bonds (NH-O6 and O6H-O7), which offers an explanation for the experimental observation that increased acetylation lowers chitosan's solubility. Taken together, the present study provides atomic-level understanding the role of acetylation plays in modulating chitosan's physiochemical properties, contributing to the rational design of chitosan-based materials with the ability to tune by its degree and pattern of acetylation. Additionally, we disseminate the improved molecular mechanics parameters that can be applied in MD studies to further understand chitosan-based materials.

摘要

壳聚糖基材料具有广泛的应用,从生物技术到制药学。最近的实验表明,壳聚糖链上的乙酰化程度和模式调节其生物和物理化学性质;然而,其分子机制尚不清楚。在这里,我们据我们所知,首次报道了从头开始的全原子分子动力学(MD)模拟,以研究不同乙酰化程度和模式下壳聚糖的自组装过程。模拟表明,10 -mer 壳聚糖链在块状或交替模式下具有 50%的乙酰化,与脱乙酰壳聚糖的纤维衍射数据一致,会形成主要由反平行链组成的有序纳米原纤维。令人惊讶的是,无论乙酰化模式如何,相同的分子间氢键介导原纤维片的形成,而水介导的相互作用稳定片层堆积。此外,乙酰化单元参与形成强的分子间氢键(NH-O6 和 O6H-O7),这解释了实验观察到的增加乙酰化降低壳聚糖溶解度的现象。总之,本研究提供了原子水平上的理解,即乙酰化在调节壳聚糖物理化学性质方面的作用,有助于合理设计具有通过乙酰化程度和模式来调节能力的壳聚糖基材料。此外,我们传播了改进的分子力学参数,可应用于 MD 研究,以进一步了解壳聚糖基材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdb3/10856132/994343b2eec3/molecules-29-00561-g001.jpg

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