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Protein engineering responses to the COVID-19 pandemic

Antigen design guided by high-resolution viral glycoprotein structures has successfully generated diverse vaccine candidates for COVID-19. Using conjugation systems to combine antigen design with computationally optimized nanoparticles, researchers have been able to display multivalent antigens with...

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Detalles Bibliográficos
Autores principales: Hsieh, Ching-Lin, McLellan, Jason S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075828/
https://www.ncbi.nlm.nih.gov/pubmed/35533563
http://dx.doi.org/10.1016/j.sbi.2022.102385
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author Hsieh, Ching-Lin
McLellan, Jason S.
author_facet Hsieh, Ching-Lin
McLellan, Jason S.
author_sort Hsieh, Ching-Lin
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description Antigen design guided by high-resolution viral glycoprotein structures has successfully generated diverse vaccine candidates for COVID-19. Using conjugation systems to combine antigen design with computationally optimized nanoparticles, researchers have been able to display multivalent antigens with beneficial substitutions that elicited robust humoral immunity with enhanced neutralization potency and breadth. Here, we discuss strategies that have been used for structure-based design and nanoparticle display to develop COVID-19 vaccine candidates as well as potential next-generation vaccine candidates to protect against SARS-CoV-2 variants and other coronaviruses that emerge into the human population.
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spelling pubmed-90758282022-05-09 Protein engineering responses to the COVID-19 pandemic Hsieh, Ching-Lin McLellan, Jason S. Curr Opin Struct Biol Article Antigen design guided by high-resolution viral glycoprotein structures has successfully generated diverse vaccine candidates for COVID-19. Using conjugation systems to combine antigen design with computationally optimized nanoparticles, researchers have been able to display multivalent antigens with beneficial substitutions that elicited robust humoral immunity with enhanced neutralization potency and breadth. Here, we discuss strategies that have been used for structure-based design and nanoparticle display to develop COVID-19 vaccine candidates as well as potential next-generation vaccine candidates to protect against SARS-CoV-2 variants and other coronaviruses that emerge into the human population. Elsevier Ltd. 2022-06 2022-04-11 /pmc/articles/PMC9075828/ /pubmed/35533563 http://dx.doi.org/10.1016/j.sbi.2022.102385 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hsieh, Ching-Lin
McLellan, Jason S.
Protein engineering responses to the COVID-19 pandemic
title Protein engineering responses to the COVID-19 pandemic
title_full Protein engineering responses to the COVID-19 pandemic
title_fullStr Protein engineering responses to the COVID-19 pandemic
title_full_unstemmed Protein engineering responses to the COVID-19 pandemic
title_short Protein engineering responses to the COVID-19 pandemic
title_sort protein engineering responses to the covid-19 pandemic
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075828/
https://www.ncbi.nlm.nih.gov/pubmed/35533563
http://dx.doi.org/10.1016/j.sbi.2022.102385
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