How Tetraspanin-Mediated Cell Entry of SARS-CoV-2 Can Dysregulate the Shedding of the ACE2 Receptor by ADAM17
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2022/02/19
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By Healy EF
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Description:COVID-19, the respiratory infection caused by the novel coronavirus SARS-CoV-2, presents a clinical picture consistent with the dysregulation of many of the pathways mediated by the metalloprotease ADAM17. ADAM17 is a sheddase that plays a key role in the modulation of ACE2, the receptor which also functions as the point of attachment leading to cell entry by the virus. This work investigates the possibility that ADAM17 dysregulation and attachment of the SARS-CoV-2 virion to the ACE2 receptor are linked events, with the latter causing the former. Tetraspanins, the transmembrane proteins that function as scaffolds for the construction of viral entry platforms, are mooted as key components in this connection. [Description provided by NIOSH]
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ISSN:0006-291X
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Pages in Document:52-56
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Volume:593
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NIOSHTIC Number:nn:20064558
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Citation:Biochem Biophys Res Commun 2022 Feb; 593:52-56
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Contact Point Address:Eamonn F Healy, Department of Chemistry, St. Edward's University, Austin, TX, 78704
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Email:healy@stedwards.edu
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Federal Fiscal Year:2022
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Performing Organization:Mount Sinai School of Medicine
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:Biochemical and Biophysical Research Communications
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End Date:20270630
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Main Document Checksum:urn:sha-512:7949d7aec4eb4344768cb8fcdd1abc651c0d5d6ea119cfa58aaa0b3d3b997615857169b99d99dd0dc288a2a4640b12c624edf048916d79804e3b7ddb18a98ea7
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