| Literature DB >> 34914049 |
Jingen Zhu1, Neeti Ananthaswamy1, Swati Jain1, Himanshu Batra1, Wei-Chun Tang1, Venigalla B Rao2.
Abstract
The COVID-19 pandemic brought to the fore the urgent need for vaccine design and delivery platforms that can be rapidly deployed for manufacture and distribution. Though the mRNA and adenoviral vector platforms have been enormously successful to control SARS-CoV-2 viral infections, it is unclear if this could be replicated against more complex pathogens or the emerging variants. Recently, we described a "universal" platform that can incorporate multiple vaccine targets into the same nanoparticle scaffold by CRISPR engineering of bacteriophage T4. A T4-COVID vaccine designed with this technology elicited broad immunogenicity and complete protection against virus challenge in a mouse model. Here, we describe the detailed methodology to generate recombinant bacteriophage T4 backbones using CRISPR that can also be broadly applicable to other bacteriophages that abundantly pervade the Earth.Entities:
Keywords: Bacteriophage T4; COVID-19 vaccine; CRISPR engineering; Nanoparticle vaccine; SARS-CoV-2 spike
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Year: 2022 PMID: 34914049 DOI: 10.1007/978-1-0716-1884-4_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745