Literature DB >> 35132600

Anticoronavirus Activity of Water-Soluble Pristine C60 Fullerenes: In Vitro and In Silico Screenings.

Vasyl Hurmach1, Maxim Platonov2, Svitlana Prylutska1,3, Zinaida Klestova4, Vsevolod Cherepanov5, Yuriy Prylutskyy6, Uwe Ritter7.   

Abstract

INTRODUCTION: The emergence of a new member of the Coronaviridae family, which caused the 2020 pandemic, requires detailed research on the evolution of coronaviruses, their structure and properties, and interaction with cells. Modern nanobiotechnologies can address the many clinical challenges posed by the COVID-19 pandemic. In particular, they offer new therapeutic approaches using biocompatible nanostructures with "specific" antiviral activity. Therefore, the nanosized spherical-like molecule (0.72 nm in diameter) composed of 60 carbon atoms, C60 fullerene, is of interest in terms of fighting coronaviruses due to its high biological activity. In here, we aim to evaluate the effectiveness of anticoronavirus action of water-soluble pristine C60 fullerene in the model and in vitro systems. As a model, apathogenic for human coronavirus, we used transmissible gastroenteritis virus of swine (TGEV), which we adapted to the BHK-21 cell culture (kidney cells of a newborn Syrian hamster).
METHODS: The shape and size of the particles present in C60 fullerene aqueous colloidal solution (C60FAS) of given concentration, as well as C60FAS stability (value of zeta potential) were studied using microscopic (STM, scanning tunneling microscopy, and AFM, atomic force microscopy) and spectroscopic (DLS, dynamic light scattering) methods. The cytopathic effect of TGEV was determined with the help of a Leica DM 750 microscope and the degree of monolayer changes in cells was assessed. The microscopy of the viral suspension was performed using a high resolution transmission electron microscope (HRTEM; JEM-1230, Japan). Finally, the search for and design of optimal possible complexes between C60 fullerene and target proteins in the structure of SARS-CoV-2 coronavirus, evaluation of their stability in the simulated cellular environment were performed using molecular dynamics and docking methods.
RESULTS: It was found that the maximum allowable cytotoxic concentration of C60 fullerene is 37.5 ± 3.0 μg/ml. The investigated C60FAS reduces the titer of coronavirus infectious activity by the value of 2.00 ± 0.08 TCID50/ml. It was shown that C60 fullerene interacts directly with SARS-CoV-2 proteins, such as RdRp (RNA-dependent RNA polymerase) and 3CLpro (3-chymotrypsin-like protease), which is critical for the life cycle of the coronavirus and, thus, inhibits its functional activity. In both cases, C60 fullerene fills the binding pocket and gets stuck there through stacking and steric interactions.
CONCLUSION: Pioneer in vitro study to identify the anticoronavirus activity of water-soluble pristine C60 fullerenes indicates that they are highly promising for further preclinical studies, since a significant inhibition of the infectious activity of swine coronavirus of transmissible gastroenteritis in BHK-21 cell culture was found. According to molecular modeling results, it was shown that C60 fullerene can create the stable complexes with 3CLpro and RdRp proteins of SARS-CoV-2 coronavirus and, thus, suppress its functional activity.
© 2021. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Entities:  

Keywords:  Anticoronavirus activity; Coronaviruses; Water-soluble pristine C60 fullerene; in vitro and in silico screening

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Year:  2021        PMID: 35132600     DOI: 10.1007/978-3-030-85109-5_10

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  15 in total

1.  [60]fullerene is a powerful antioxidant in vivo with no acute or subacute toxicity.

Authors:  Najla Gharbi; Monique Pressac; Michelle Hadchouel; Henri Szwarc; Stephen R Wilson; Fathi Moussa
Journal:  Nano Lett       Date:  2005-12       Impact factor: 11.189

2.  QXP: powerful, rapid computer algorithms for structure-based drug design.

Authors:  C McMartin; R S Bohacek
Journal:  J Comput Aided Mol Des       Date:  1997-07       Impact factor: 3.686

3.  A transmissible gastroenteritis in pigs.

Authors:  L P DOYLE; L M HUTCHINGS
Journal:  J Am Vet Med Assoc       Date:  1946-04       Impact factor: 1.936

4.  Fullerenes in liquid media: an unsettling intrusion into the solution chemistry.

Authors:  Nikolay O McHedlov-Petrossyan
Journal:  Chem Rev       Date:  2013-04-24       Impact factor: 60.622

5.  CHARMM36 all-atom additive protein force field: validation based on comparison to NMR data.

Authors:  Jing Huang; Alexander D MacKerell
Journal:  J Comput Chem       Date:  2013-07-06       Impact factor: 3.376

6.  Scavenging of reactive oxygen and nitrogen species with nanomaterials.

Authors:  Carolina A Ferreira; Dalong Ni; Zachary T Rosenkrans; Weibo Cai
Journal:  Nano Res       Date:  2018-05-26       Impact factor: 8.897

7.  Replication of transmissible gastroenteritis coronavirus (TGEV) in swine alveolar macrophages.

Authors:  H Laude; B Charley; J Gelfi
Journal:  J Gen Virol       Date:  1984-02       Impact factor: 3.891

8.  A viral gastroenteritis of Ontario swine. 1. Clinical illness and recovery of the virus.

Authors:  J Ditchfield; H G Pearce; R D Jolly; R A Curtis
Journal:  Can J Comp Med Vet Sci       Date:  1967-08

9.  Fullerene C60 Penetration into Leukemic Cells and Its Photoinduced Cytotoxic Effects.

Authors:  D Franskevych; K Palyvoda; D Petukhov; S Prylutska; I Grynyuk; C Schuetze; L Drobot; O Matyshevska; U Ritter
Journal:  Nanoscale Res Lett       Date:  2017-01-13       Impact factor: 4.703

10.  Structure of the SARS-CoV nsp12 polymerase bound to nsp7 and nsp8 co-factors.

Authors:  Robert N Kirchdoerfer; Andrew B Ward
Journal:  Nat Commun       Date:  2019-05-28       Impact factor: 14.919

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