| Literature DB >> 35800465 |
Audrey Le Bas1, Halina Mikolajek2, Jiandong Huo1,3,1, Joshua Dormon1, James H Naismith1,3, Raymond J Owens1,3.
Abstract
The receptor binding domain (RBD) of the spike protein of SARS-CoV-2 binds angiotensin converting enzyme-2 (ACE-2) on the surface of epithelial cells, leading to fusion, and entry of the virus into the cell. This interaction can be blocked by the binding of llama-derived nanobodies (VHHs) to the RBD, leading to virus neutralisation. Structural analysis of VHH-RBD complexes by X-ray crystallography enables VHH epitopes to be precisely mapped, and the effect of variant mutations to be interpreted and predicted. Key to this is a protocol for the reproducible production and crystallization of the VHH-RBD complexes. Based on our experience, we describe a workflow for expressing and purifying the proteins, and the screening conditions for generating diffraction quality crystals of VHH-RBD complexes. Production and crystallization of protein complexes takes approximately twelve days, from construction of vectors to harvesting and freezing crystals for data collection.Entities:
Keywords: Crystallization; Nanobodies; Protein purification; Receptor Binding Domain; SARS CoV-2
Year: 2022 PMID: 35800465 PMCID: PMC9090526 DOI: 10.21769/BioProtoc.4406
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325