探索人类α-突触核蛋白与聚乙烯纳米塑料的相互作用:计算建模和实验证实的启示。

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Neha Tripathi, Florent Saudrais, Mona Rysak, Laura Pieri, Serge Pin, Guido Roma, Jean-Philippe Renault, Yves Boulard
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引用次数: 0

摘要

塑料,尤其是微塑料(MPs)和纳米塑料(NP),因其化学稳定性高,已成为环境和健康方面的主要问题。高疏水性塑料通过与生物大分子的可逆相互作用进入生物体内,形成生物噬菌体。继最近有关塑料突破血脑屏障的报道之后,我们利用分子动力学模拟和实验方法评估了人类α-突触核蛋白(hαSn)与聚乙烯基(PE)塑料的结合行为。研究结果提供了三个重要发现:(i) hαSn 从开放螺旋构象转变为紧凑构象,增强了分子内相互作用;(ii) 非氧化聚乙烯 NP(NPnonox)迅速吸附 hαSn,动态光散射和吸附等温线的实验数据证明了这一点,并改变了其结构;(iii) 氧化 NP(NPox)未能捕获 hαSn。这些相互作用由 hαSn 的 N 端结构域主导,疏水性氨基酸对其有主要贡献。这些发现引起了人们对 NP 蛋白相互作用对人类健康的潜在药理作用的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the Interaction of Human α-Synuclein with Polyethylene Nanoplastics: Insights from Computational Modeling and Experimental Corroboration.

Plastics, particularly microplastics (MPs) and nanoplastics (NP), have become major environmental and health concerns due to their high chemical stability. The highly hydrophobic plastics enter living organisms through reversible interactions with biomolecules, forming biocoronas. Following recent reports on plastics breaching the blood-brain barrier, the binding behavior of human α-synuclein (hαSn) with polyethylene-based (PE) plastics was evaluated by using molecular dynamics simulations and experimental methods. The results provided three important findings: (i) hαSn transitions from an open helical to a compact conformation, enhancing intramolecular interactions, (ii) nonoxidized PE NPs (NPnonox) rapidly adsorb hαSn, as supported by experimental data from dynamic light scattering and adsorption isotherms, altering its structure, and (iii) the oxidized NP (NPox) failed to capture hαSn. These interactions were dominated by the N-terminal domain of hαSn, with major contributions from hydrophobic amino acids. These findings raise concerns about the potential pharmacological effects of NP-protein interactions on human health.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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