4.7 Article

Effect of carbonaceous ultrafine particles on the structure and oligomerization of A?42 peptide

期刊

ENVIRONMENTAL POLLUTION
卷 323, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2023.121273

关键词

Carbonaceous ultrafine particles; Amyloid beta peptide; Alzheimer?s diseases; Environmental nanotoxicology; Oligomerization; Protein structure

向作者/读者索取更多资源

The impact of air pollutants, specifically ultrafine particles (UFPs), on human health is a growing concern. This study used molecular dynamics simulations to investigate the effects of carbonaceous UFPs on the structure and oligomerization of A beta 42 peptides, which are associated with the development of Alzheimer's disease (AD). The results showed that the presence of carbonaceous UFPs promoted the aggregation and unfolding of the A beta 42 peptides, suggesting a potential link between air pollution and the progression of AD.
The impact of pervasive air pollutants on human health is a growing concern in scientific communities. Among different air pollutants, ultrafine particles (UFPs; with aerodynamic diameter <100 nm) might pass through biological barriers and have a severe impact on human health, including early progression of neurodegenerative diseases such as Alzheimer's disease (AD). A significant fraction of UFPs consists of carbonaceous compounds, composed of elemental and organic carbon (EC and OC). While in-vivo experimental studies showed the neurotoxicity of typical OC and polycyclic aromatic hydrocarbons (PAHs), the molecular interactions involved in the progression of AD remain unclear. In this study, molecular dynamics simulations were performed to inves-tigate the impact of carbonaceous UFPs on the structure of the A beta 42 monomer and the oligomerization of four A beta 42 peptides, associated with the development of AD. For the simulations, a fullerene (C60) was used for the modeling of EC, while benzo [a]pyrene (B[a]P) was used for the modeling of OC. The results revealed that the presence of C60 accelerated the tetramerization of A beta 42 peptides by 2.5 times, while C60/B[a]P promoted the unfolding of the peptide monomer showing the strongest interactions with the A beta 42 monomer. Similarly, C60/4B [a]P decreased the number of helices in the secondary structure of the peptide monomer by 60%. The simplified UFP models in this study, promoted the early aggregation of peptides to dimers, suggesting the progression of AD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据