JOURNAL ARTICLE

COVID 19: Camostat and The Role of Serine Protease Entry Inhibitor TMPRSS2

Abstract

According to the latest research, the novel coronavirus uses the protein angiotensin-converting enzyme 2 (ACE-2) as a receptor for docking to the host cell. Essential for entry is the priming of the spike (S) protein of the virus by host cell proteases. A broadly based team led by infection biologists from the German Primate Centre and with the participation of the Charité Hospital in Berlin, the Hanover Veterinary University Foundation, the BG-UnfallklinikMurnau, the LMU Munich, the Robert Koch Institute and the German Centre for Infection Research wanted to find out how SARS-CoV-2 enters host cells and how this process can be blocked [1]. They have published their findings in the journal "Cell" [1]. The team of scientists was initially able to confirm that SARS-CoV-2 docks to the host cell via the ACE-2 receptor. They also identified Transmembrane serine protease 2 (TMPRSS2) as the cellular protein responsible for entry into the cell [1-3].

Keywords:
TMPRSS2 Proteases Serine protease Protease Coronavirus disease 2019 (COVID-19) Serine Proteinase Inhibitors Biology Transmembrane protein Protease inhibitor (pharmacology) Receptor Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Virology Serine Angiotensin-converting enzyme 2 Cell Enzyme Virus Biochemistry Medicine Infectious disease (medical specialty) Internal medicine

Metrics

16
Cited By
0.46
FWCI (Field Weighted Citation Impact)
3
Refs
0.75
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

SARS-CoV-2 and COVID-19 Research
Health Sciences →  Medicine →  Infectious Diseases
COVID-19 Clinical Research Studies
Health Sciences →  Medicine →  Infectious Diseases
Long-Term Effects of COVID-19
Health Sciences →  Medicine →  Neurology
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