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Review
. 2021 Aug:54:101461.
doi: 10.1016/j.cocis.2021.101461. Epub 2021 Apr 23.

Biomolecular interactions with nanoparticles: applications for coronavirus disease 2019

Affiliations
Review

Biomolecular interactions with nanoparticles: applications for coronavirus disease 2019

Mohammed A H Farouq et al. Curr Opin Colloid Interface Sci. 2021 Aug.

Abstract

Nanoparticles are small particles sized 1-100 nm, which have a large surface-to-volume ratio, allowing efficient adsorption of drugs, proteins, and other chemical compounds. Consequently, functionalized nanoparticles have potential diagnostic and therapeutic applications. A variety of nanoparticles have been studied, including those constructed from inorganic materials, biopolymers, and lipids. In this review, we focus on recent work targeting the severe acute respiratory syndrome coronavirus 2 virus that causes coronavirus disease (COVID-19). Understanding the interactions between coronavirus-specific proteins (such as the spike protein and its host cell receptor angiotensin-converting enzyme 2) with different nanoparticles paves the way to the development of new therapeutics and diagnostics that are urgently needed for the fight against COVID-19, and indeed for related future viral threats that may emerge.

Keywords: COVID-19; Diagnostics; Nanoparticles; Proteins; SARS-CoV-2; Therapeutics.

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Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this article.

Figures

Image 1
Graphical abstract
Figure 1
Figure 1
A schematic diagram showing drug loading options in NP targeted drug delivery.
Figure 2
Figure 2
Diagram showing the structural proteins of the SARS-CoV-2 virus.
Figure 3
Figure 3
Interaction between the ACE2 receptor (blue) and the S protein RBD (red). Inset shows key interacting residues between the ACE2 receptor. The crystal structure was obtained from the Protein Databank (PDB entry 6M0J [38]). The crystal structure was viewed and analyzed using VMD (Visual Molecular Dynamics 1.9.1).

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