| Literature DB >> 34859134 |
Cecilia Di Genova1, Alex Sampson2, Simon Scott1, Diego Cantoni1, Martin Mayora-Neto1, Emma Bentley3, Giada Mattiuzzo3, Edward Wright4, Mariliza Derveni4, Bethany Auld4, Bill T Ferrara5, Dale Harrison5, Mohamed Said5, Arwa Selim5, Elinor Thompson5, Craig Thompson6, George Carnell2, Nigel Temperton1.
Abstract
This protocol details a rapid and reliable method for the production and titration of high-titre viral pseudotype particles with the SARS-CoV-2 spike protein (and D614G or other variants of concern, VOC) on a lentiviral vector core, and use for neutralisation assays in target cells expressing angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2). It additionally provides detailed instructions on substituting in new spike variants via gene cloning, lyophilisation and storage/shipping considerations for wide deployment potential. Results obtained with this protocol show that SARS-CoV-2 pseudotypes can be produced at equivalent titres to SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV) pseudotypes, neutralised by human convalescent plasma and monoclonal antibodies, and stored at a range of laboratory temperatures and lyophilised for distribution and subsequent application.Entities:
Keywords: COVID-19; Lentiviral pseudotype; Pseudotype lyophilisation; SARS-CoV-2 coronavirus; Spike variants; Virus neutralisation
Year: 2021 PMID: 34859134 PMCID: PMC8595416 DOI: 10.21769/BioProtoc.4236
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325