4.7 Article

Lethal Interactions of SARS-CoV-2 with Graphene Oxide: Implications for COVID-19 Treatment

Journal

ACS APPLIED NANO MATERIALS
Volume 4, Issue 11, Pages 11881-11887

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c02446

Keywords

graphene oxide; SARS-CoV-2; antiviral; surface functional groups; viral protein decomposition

Funding

  1. KAKENHI from the Ministry of Education, Culture, Sports, Science, and Technology, Japan [JP17H01200]
  2. JSPS Leading Initiative for Excellent Young Researchers (LEADER)
  3. AMED Research Program on Emerging and Reemerging Infectious Diseases [20fk0108413]
  4. JST A-STEP [JPMJTM20SL]
  5. Takeda Science Foundation
  6. Mitsubishi Foundation
  7. Shin-Nihon Foundation of Advanced Medical Research
  8. Kumamoto University COVID-19 Research Projects (AMABIE)
  9. Intercontinental Research and Educational Platform Aiming for Eradication of HIV/AIDS

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Research on the inactivation of SARS-CoV-2 using graphene oxide (GO) shows promising antiviral effects, with GO effectively neutralizing the virus and potentially inhibiting its ability to infect human cells by damaging the S protein. This opens up possibilities for the development of effective anti-SARS-CoV-2 face masks and protective surfaces/coatings based on GO nanosheets.
The rapid transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-driven infection signifies an ultimate challenge to global health, and the development of effective strategies for preventing and/or mitigating its effects are of the utmost importance. In the current study, an in-depth investigation for the understanding of the SARS-CoV-2 inactivation route using graphene oxide (GO) is presented. We focus on the antiviral effect of GO nanosheets on three SARS-CoV-2 strains: Wuhan, B.1.1.7 (U.K. variant), and P.1 (Brazilian variant). Plaque assay and real-time reverse transcription-polymerase chain reaction (RT-PCR) showed that 50 and 98% of the virus in a supernatant could be cleared following incubation with GO (100 mu g/mL) for 1 and 60 min, respectively. Transmission electron microscopy (TEM) analysis and protein (spike (S) and nucleocapsid (N) proteins) decomposition evaluation confirm a two-step virus inactivation mechanism that includes (i) adsorption of the positively charged spike of SARS-CoV-2 on the negatively charged GO surface and (ii) neutralization/inactivation of the SARS-CoV-2 on the surface of GO through decomposition of the viral protein. As the interaction of S protein with human angiotensin-converting enzyme 2 (ACE2) is required for SARS-CoV-2 to enter into human cells, the damage to the S protein using GO makes it a potential candidate for use in contributing to the inhibition of the worldwide spread of SARS-CoV-2. Specifically, our findings provide the potential for the construction of an effective anti-SARS-CoV-2 face mask using a GO nanosheet, which could contribute greatly to preventing the spread of the virus. In addition, as the effect of surface contamination can be severe in the spreading of SARS-CoV-2, the development of efficient anti-SARS-CoV-2 protective surfaces/coatings based on GO nanosheets could play a significant role in controlling the spread of the virus through the utilization of GO-based nonwoven cloths, filters, and so on.

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