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Protein engineering responses to the COVID-19 pandemic.
Hsieh, Ching-Lin; McLellan, Jason S.
  • Hsieh CL; Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA 78712.
  • McLellan JS; Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA 78712. Electronic address: jmclellan@austin.utexas.edu.
Curr Opin Struct Biol ; 74: 102385, 2022 06.
Article in English | MEDLINE | ID: covidwho-1783716
ABSTRACT
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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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Humans Language: English Journal: Curr Opin Struct Biol Journal subject: Molecular Biology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Humans Language: English Journal: Curr Opin Struct Biol Journal subject: Molecular Biology Year: 2022 Document Type: Article