bioRxiv (Cold Spring Harbor Laboratory) · 2020 · 32 citations · 41 references
Life SciencesImmunologyInfectious DiseasesMolecular VirologyVaccinologyVirologyNanomaterials For Drug DeliveryNanomedicineNanoparticle-based ImmunotechnologyProtein DeliveryVaccine DeliveryVaccine PlatformsNanobodiesNanobody DiscoveryNanobody DisplayNanoparticle Delivery VectorsPhage Display LibrariesPhage Display ScreeningSars-cov-2 InfectionStability Profile Assessment
Abstract The outbreak of COVID-19 has emerged as a global pandemic. The unprecedented scale and severity call for rapid development of effective prophylactics or therapeutics. We here reported Nanobody (Nb) phage display libraries derived from four camels immunized with the SARS-CoV-2 spike receptor-binding domain (RBD), from which 381 Nbs were identified to recognize SARS-CoV-2-RBD. Furthermore, seven Nbs were shown to block interaction of human angiotensin converting enzyme 2 (ACE2) with SARS-CoV-2-RBD-variants, bat-SL-CoV-WIV1-RBD and SARS-CoV-1-RBD. Among the seven candidates, Nb11-59 exhibited the highest activity against authentic SARS-CoV-2 with ND 50 of 0.55 μg/mL. Nb11-59 can be produced on a large-scale in Pichia pastoris , with 20 g/L titer and 99.36% purity. It also showed good stability profile, and nebulization did not impact its stability. Overall, Nb11-59 might be a promising prophylactic and therapeutic molecule against COVID-19, especially through inhalation delivery. Graphical Abstract
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