Abstract
Viral internalization is aided by host cell surface receptors. In the case of SARS-CoV-2 and SARS-CoV, the primary host receptor is the angiotensin-converting enzyme 2 (ACE2). Considering the disparities in the transmission rate and viral tropism of the two coronaviruses, additional host factors were suspected. Recently, a novel host factor for SARS-CoV-2 entry, neuropilin-1 (NRP-1) has been identified. These receptors potentiate viral infection in the presence of other host factors like ACE2. Through its C-end rule (CendR) motif exposed following furin processing, the SARS-CoV-2 spike protein binds to the CendR pocket of NRP-1 and achieves cell entry through endocytosis. The binding of SARS-CoV-2 spike protein to the NRP-1 receptor interferes with the docking of its endogenous ligand VEGF-A, signaling that would otherwise promote nociception. This review looks at the function of neuropilins and how it contributes to SARS-CoV-2 infection and nociception.
Original language | English |
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Pages (from-to) | 1889-1895 |
Number of pages | 7 |
Journal | Computational and Structural Biotechnology Journal |
Volume | 19 |
DOIs | |
Publication status | Published - Jan 2021 |
Keywords
- Host factor
- Neuropilin
- Nociception
- SARS-CoV-2
- Spike protein
- VEGF-A
ASJC Scopus subject areas
- Biotechnology
- Biophysics
- Structural Biology
- Biochemistry
- Genetics
- Computer Science Applications