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Neuropilins: C-end rule peptides and their association with nociception and COVID-19

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 wer...

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Detalles Bibliográficos
Autores principales: Jobe, Amie, Vijayan, Ranjit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997051/
https://www.ncbi.nlm.nih.gov/pubmed/33815686
http://dx.doi.org/10.1016/j.csbj.2021.03.025
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author Jobe, Amie
Vijayan, Ranjit
author_facet Jobe, Amie
Vijayan, Ranjit
author_sort Jobe, Amie
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description 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.
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spelling pubmed-79970512021-03-29 Neuropilins: C-end rule peptides and their association with nociception and COVID-19 Jobe, Amie Vijayan, Ranjit Comput Struct Biotechnol J Review Article 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. Research Network of Computational and Structural Biotechnology 2021-03-26 /pmc/articles/PMC7997051/ /pubmed/33815686 http://dx.doi.org/10.1016/j.csbj.2021.03.025 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Jobe, Amie
Vijayan, Ranjit
Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title_full Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title_fullStr Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title_full_unstemmed Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title_short Neuropilins: C-end rule peptides and their association with nociception and COVID-19
title_sort neuropilins: c-end rule peptides and their association with nociception and covid-19
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997051/
https://www.ncbi.nlm.nih.gov/pubmed/33815686
http://dx.doi.org/10.1016/j.csbj.2021.03.025
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