8G72
SARS-CoV-2 spike/Nb2 complex with 1 RBD up (local refinement at 5.6 A)
Summary for 8G72
Entry DOI | 10.2210/pdb8g72/pdb |
EMDB information | 29792 29793 29794 29795 29796 29797 29798 29799 29802 29803 29804 29805 29806 |
Descriptor | Nanosota-2, Spike glycoprotein (2 entities in total) |
Functional Keywords | sars-cov-2, viral protein-immune system complex, nanobody, viral protein/immune system |
Biological source | Vicugna pacos (alpaca) More |
Total number of polymer chains | 2 |
Total formula weight | 153640.49 |
Authors | |
Primary citation | Ye, G.,Pan, R.,Bu, F.,Zheng, J.,Mendoza, A.,Wen, W.,Du, L.,Spiller, B.,Wadzinski, B.E.,Liu, B.,Perlman, S.,Li, F. Discovery of Nanosota-2, -3, and -4 as super potent and broad-spectrum therapeutic nanobody candidates against COVID-19. J.Virol., 97:e0144823-e0144823, 2023 Cited by PubMed Abstract: The COVID-19 pandemic exposed limitations of conventional antibodies as therapeutics, including high cost, limited potency, ineffectiveness against new viral variants, and primary reliance on injection-only delivery. Nanobodies are single-domain antibodies with therapeutic potentials. We discovered three anti-SARS-CoV-2 nanobodies, named Nanosota-2, -3, and -4, from an immunized alpaca. Nanosota-2 is super potent against prototypic SARS-CoV-2, Nanosota-3 is highly potent against the omicron variant, and Nanosota-4 is effective against both SARS-CoV-1 and SARS-CoV-2. In addition to their super potency and combined broad antiviral spectrum, these nanobodies are cost-effective, can be easily adapted to new viral variants through phage display, and can potentially be administered as inhalers. The Nanosota series are powerful therapeutic candidates to combat circulating SARS-CoV-2 and prepare for possible future coronavirus pandemics. PubMed: 37855638DOI: 10.1128/jvi.01448-23 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (5.6 Å) |
Structure validation
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