Low Dose of Ti3C2 MXene Quantum Dots Mitigate SARS‐CoV‐2 Infection

Author:

Yilmazer Açelya12ORCID,Alagarsamy Keshav Narayan3,Gokce Cemile1,Summak Gokce Yagmur2,Rafieerad Alireza3,Bayrakdar Fatma4,Ozturk Berfin Ilayda1,Aktuna Suleyman5,Delogu Lucia Gemma67,Unal Mehmet Altay2,Dhingra Sanjiv3

Affiliation:

1. Department of Biomedical Engineering Ankara University Golbasi Ankara 06830 Turkey

2. Stem Cell Institute Ankara University Balgat Ankara 06520 Turkey

3. Institute of Cardiovascular Sciences St. Boniface Hospital Albrechtsen Research Centre Department of Physiology and Pathophysiology Rady Faculty of Health Sciences University of Manitoba Winnipeg R3T 2N2 Canada

4. Microbiology References Laboratory Ministry of Health General Directorate of Public Health Ankara 06100 Turkey

5. Department of Medical Genetics Faculty of Medicine Yuksek Ihtisas University Ankara 06530 Turkey

6. Department of Biomedical Sciences University of Padua Padua 35122 Italy

7. New York University Abu Dhabi Abu Dhabi 129188 United Arab Emirates

Abstract

AbstractMXene QDs (MQDs) have been effectively used in several fields of biomedical research. Considering the role of hyperactivation of immune system in infectious diseases, especially in COVID‐19, MQDs stand as a potential candidate as a nanotherapeutic against viral infections. However, the efficacy of MQDs against SARS‐CoV‐2 infection has not been tested yet. In this study, Ti3C2 MQDs are synthesized and their potential in mitigating SARS‐CoV‐2 infection is investigated.  Physicochemical characterization suggests that MQDs are enriched with abundance of bioactive functional groups such as oxygen, hydrogen, fluorine, and chlorine groups as well as surface titanium oxides. The efficacy of MQDs is tested in VeroE6 cells infected with SARS‐CoV‐2. These data demonstrate that the treatment with MQDs is able to mitigate multiplication of virus particles, only at very low doses such as 0,15 µg mL−1. Furthermore, to understand the mechanisms of MQD‐mediated anti‐COVID properties, global proteomics analysis are performed and determined differentially expressed proteins between MQD‐treated and untreated cells. Data reveal that MQDs interfere with the viral life cycle through different mechanisms including the Ca2+ signaling pathway, IFN‐α response, virus internalization, replication, and translation. These findings suggest that MQDs can be employed to develop future immunoengineering‐based nanotherapeutics strategies against SARS‐CoV‐2 and other viral infections.

Funder

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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