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SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs

The SARS-CoV-2 3a protein is a putative ion channel implicated in virus life cycle and pathogenesis. We recently expressed, purified, and reconstituted 3a into lipid nanodiscs to solve its structure by cryo-EM to 2.1 Å resolution. In this chapter, we describe methods we developed in order to facilit...

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Detalles Bibliográficos
Autores principales: Kern, David M., Brohawn, Stephen G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839409/
https://www.ncbi.nlm.nih.gov/pubmed/34099172
http://dx.doi.org/10.1016/bs.mie.2020.12.020
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author Kern, David M.
Brohawn, Stephen G.
author_facet Kern, David M.
Brohawn, Stephen G.
author_sort Kern, David M.
collection PubMed
description The SARS-CoV-2 3a protein is a putative ion channel implicated in virus life cycle and pathogenesis. We recently expressed, purified, and reconstituted 3a into lipid nanodiscs to solve its structure by cryo-EM to 2.1 Å resolution. In this chapter, we describe methods we developed in order to facilitate the study of this protein in other laboratories. We emphasize factors that enabled rapid progression from gene sequence to reconstituted protein (3 weeks in the case of 3a) and provide general observations and tips for adapting these protocols to other membrane proteins of interest.
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spelling pubmed-78394092021-01-28 SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs Kern, David M. Brohawn, Stephen G. Methods Enzymol Article The SARS-CoV-2 3a protein is a putative ion channel implicated in virus life cycle and pathogenesis. We recently expressed, purified, and reconstituted 3a into lipid nanodiscs to solve its structure by cryo-EM to 2.1 Å resolution. In this chapter, we describe methods we developed in order to facilitate the study of this protein in other laboratories. We emphasize factors that enabled rapid progression from gene sequence to reconstituted protein (3 weeks in the case of 3a) and provide general observations and tips for adapting these protocols to other membrane proteins of interest. Elsevier Inc. 2021 2021-01-27 /pmc/articles/PMC7839409/ /pubmed/34099172 http://dx.doi.org/10.1016/bs.mie.2020.12.020 Text en Copyright © 2021 Elsevier Inc. 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
Kern, David M.
Brohawn, Stephen G.
SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title_full SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title_fullStr SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title_full_unstemmed SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title_short SARS-CoV-2 3a expression, purification, and reconstitution into lipid nanodiscs
title_sort sars-cov-2 3a expression, purification, and reconstitution into lipid nanodiscs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839409/
https://www.ncbi.nlm.nih.gov/pubmed/34099172
http://dx.doi.org/10.1016/bs.mie.2020.12.020
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