| Autor: |
Walter, J D, Hutter, C A, Garaeva, A A, Scherer, M, Zimmermann, I, Wyss, M, Rheinberger, J, Ruedin, Y, Earp, J C, Egloff, P, Sorgenfrei, M, Hürlimann, L M, Gonda, I, Meier, G., Remme, S, Thavarasah, S, van der Geest, G, Bruggman, R, Zimmer, G, Slotboom, Dirk, Paulino, Cristina, Plattet, P, Seeger, M A |
| Přispěvatelé: |
Enzymology, Electron Microscopy |
| Jazyk: |
angličtina |
| Popis: |
The ongoing COVID-19 pandemic represents an unprecedented global health crisis. Here, we report the identification of a synthetic nanobody (sybody) pair (Sb#15 and Sb#68) that can bind simultaneously to the SARS-CoV-2 spike-RBD and efficiently neutralize pseudotyped and live-viruses by interfering with ACE2 interaction. Two spatially-discrete epitopes identified by cryo-EM translated into the rational design of bispecific and tri-bispecific fusions constructs, exhibiting up to 100- and 1000-fold increase in neutralization potency. Cryo-EM of the sybody-spike complex further revealed a novel up-out RBD conformation. While resistant viruses emerged rapidly in the presence of single binders, no escape variants were observed in presence of the bispecific sybody. The multivalent bispecific constructs further increased the neutralization potency against globally-circulating SARS-CoV-2 variants of concern. Our study illustrates the power of multivalency and biparatopic nanobody fusions for the development of clinically relevant therapeutic strategies that mitigate the emergence of new SARS-CoV-2 escape mutants. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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