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Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19

COVID-19 is primarily known as a respiratory disease caused by SARS-CoV-2. However, neurological symptoms such as memory loss, sensory confusion, severe headaches, and even stroke are reported in up to 30% of cases and can persist even after the infection is over (long COVID). These neurological sym...

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Autores principales: Charnley, Mirren, Islam, Saba, Bindra, Guneet K., Engwirda, Jeremy, Ratcliffe, Julian, Zhou, Jiangtao, Mezzenga, Raffaele, Hulett, Mark D., Han, Kyunghoon, Berryman, Joshua T., Reynolds, Nicholas P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189797/
https://www.ncbi.nlm.nih.gov/pubmed/35697699
http://dx.doi.org/10.1038/s41467-022-30932-1
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author Charnley, Mirren
Islam, Saba
Bindra, Guneet K.
Engwirda, Jeremy
Ratcliffe, Julian
Zhou, Jiangtao
Mezzenga, Raffaele
Hulett, Mark D.
Han, Kyunghoon
Berryman, Joshua T.
Reynolds, Nicholas P.
author_facet Charnley, Mirren
Islam, Saba
Bindra, Guneet K.
Engwirda, Jeremy
Ratcliffe, Julian
Zhou, Jiangtao
Mezzenga, Raffaele
Hulett, Mark D.
Han, Kyunghoon
Berryman, Joshua T.
Reynolds, Nicholas P.
author_sort Charnley, Mirren
collection PubMed
description COVID-19 is primarily known as a respiratory disease caused by SARS-CoV-2. However, neurological symptoms such as memory loss, sensory confusion, severe headaches, and even stroke are reported in up to 30% of cases and can persist even after the infection is over (long COVID). These neurological symptoms are thought to be produced by the virus infecting the central nervous system, however we don’t understand the molecular mechanisms triggering them. The neurological effects of COVID-19 share similarities to neurodegenerative diseases in which the presence of cytotoxic aggregated amyloid protein or peptides is a common feature. Following the hypothesis that some neurological symptoms of COVID-19 may also follow an amyloid etiology we identified two peptides from the SARS-CoV-2 proteome that self-assemble into amyloid assemblies. Furthermore, these amyloids were shown to be highly toxic to neuronal cells. We suggest that cytotoxic aggregates of SARS-CoV-2 proteins may trigger neurological symptoms in COVID-19.
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spelling pubmed-91897972022-06-15 Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19 Charnley, Mirren Islam, Saba Bindra, Guneet K. Engwirda, Jeremy Ratcliffe, Julian Zhou, Jiangtao Mezzenga, Raffaele Hulett, Mark D. Han, Kyunghoon Berryman, Joshua T. Reynolds, Nicholas P. Nat Commun Article COVID-19 is primarily known as a respiratory disease caused by SARS-CoV-2. However, neurological symptoms such as memory loss, sensory confusion, severe headaches, and even stroke are reported in up to 30% of cases and can persist even after the infection is over (long COVID). These neurological symptoms are thought to be produced by the virus infecting the central nervous system, however we don’t understand the molecular mechanisms triggering them. The neurological effects of COVID-19 share similarities to neurodegenerative diseases in which the presence of cytotoxic aggregated amyloid protein or peptides is a common feature. Following the hypothesis that some neurological symptoms of COVID-19 may also follow an amyloid etiology we identified two peptides from the SARS-CoV-2 proteome that self-assemble into amyloid assemblies. Furthermore, these amyloids were shown to be highly toxic to neuronal cells. We suggest that cytotoxic aggregates of SARS-CoV-2 proteins may trigger neurological symptoms in COVID-19. Nature Publishing Group UK 2022-06-13 /pmc/articles/PMC9189797/ /pubmed/35697699 http://dx.doi.org/10.1038/s41467-022-30932-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Charnley, Mirren
Islam, Saba
Bindra, Guneet K.
Engwirda, Jeremy
Ratcliffe, Julian
Zhou, Jiangtao
Mezzenga, Raffaele
Hulett, Mark D.
Han, Kyunghoon
Berryman, Joshua T.
Reynolds, Nicholas P.
Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title_full Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title_fullStr Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title_full_unstemmed Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title_short Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19
title_sort neurotoxic amyloidogenic peptides in the proteome of sars-cov2: potential implications for neurological symptoms in covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189797/
https://www.ncbi.nlm.nih.gov/pubmed/35697699
http://dx.doi.org/10.1038/s41467-022-30932-1
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