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http://purl.uniprot.org/citations/34338634http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34338634http://www.w3.org/2000/01/rdf-schema#comment"Combating the COVID-19 pandemic requires potent and low-cost therapeutics. We identified a series of single-domain antibodies (i.e., nanobody), Nanosota-1, from a camelid nanobody phage display library. Structural data showed that Nanosota-1 bound to the oft-hidden receptor-binding domain (RBD) of SARS-CoV-2 spike protein, blocking viral receptor angiotensin-converting enzyme 2 (ACE2). The lead drug candidate possessing an Fc tag (Nanosota-1C-Fc) bound to SARS-CoV-2 RBD ~3000 times more tightly than ACE2 did and inhibited SARS-CoV-2 pseudovirus ~160 times more efficiently than ACE2 did. Administered at a single dose, Nanosota-1C-Fc demonstrated preventive and therapeutic efficacy against live SARS-CoV-2 infection in both hamster and mouse models. Unlike conventional antibodies, Nanosota-1C-Fc was produced at high yields in bacteria and had exceptional thermostability. Pharmacokinetic analysis of Nanosota-1C-Fc documented an excellent in vivo stability and a high tissue bioavailability. As effective and inexpensive drug candidates, Nanosota-1 may contribute to the battle against COVID-19."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.org/dc/terms/identifier"doi:10.7554/elife.64815"xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Li F."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Du L."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Perlman S."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Shi K."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Zheng J."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Wan Y."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Ye G."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Aihara H."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Shang J."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Tai W."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Gallant J."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Vickers M."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Odle A."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"Massey C."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/author"LeBeau A."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/name"Elife"xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/pages"e64815"xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/title"The development of Nanosota-1 as anti-SARS-CoV-2 nanobody drug candidates."xsd:string
http://purl.uniprot.org/citations/34338634http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/34338634http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34338634
http://purl.uniprot.org/citations/34338634http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34338634