In Silico Analysis of Nanoplastics' and β-amyloid Fibrils' Interactions

Molecules. 2023 Jan 2;28(1):388. doi: 10.3390/molecules28010388.

Abstract

Plastic pollution has become a global environmental threat, which leads to an increasing concern over the consequences of plastic exposition on global health. Plastic nanoparticles have been shown to influence the folding of proteins and influence the formation of aberrant amyloid proteins, therefore potentially triggering the development of systemic and local amyloidosis. This work aims to study the interaction between nanoplastics and β-amyloid fibrils to better understand the potential role of nanoplastics in the outbreak of neurodegenerative disorders. Using microsecond-long coarse-grained molecular dynamics simulations, we investigated the interactions between neutral and charged nanoparticles made of the most common plastic materials (i.e., polyethylene, polypropylene, and polystyrene) and β-amyloid fibrils. We observe that the occurrence of contacts, region of amyloid fibril involved, and specific amino acids mediating the interaction depend on the type and charge of the nanoparticles.

Keywords: amyloids; coarse-grained models; molecular dynamics simulations; nanoplastics; protein aggregation.

MeSH terms

  • Amyloid beta-Peptides / metabolism
  • Amyloid* / chemistry
  • Amyloidogenic Proteins
  • Amyloidosis*
  • Humans
  • Microplastics
  • Molecular Dynamics Simulation

Substances

  • Amyloid
  • Microplastics
  • Amyloidogenic Proteins
  • Amyloid beta-Peptides

Grants and funding

We acknowledge the CINECA award under the ISCRA initiative (Grant code IsB26_W2EB and IsCa2_REZYME) for the availability of high-performance computing resources and support.