Biolegend, 560304, Biotinylated Recombinant SARS-CoV-2 B.1.1.7 Spike Protein S1 (carrier-free)

The severe acute respiratory syndrome coronavirus (SARS-CoV-2) is a respiratory virus which causes coronavirus disease 2019 (COVID-19). The coronavirus spike (S) glycoprotein is a class I viral fusion protein on the outer envelope of the virion that plays a critical role in viral infection by recognizing host cell receptors and mediating fusion of the viral and cellular membranes. The S glycoprotein is synthesized as a precursor protein consisting of ~1,300 amino acids that is then cleaved into an amino (N)-terminal S1 subunit (~700 amino acids) and a carboxyl (C)-terminal S2 subunit (~600 amino acids). Three S1/S2 heterodimers assemble to form a trimer spike protruding from the viral envelope. The S1 subunit contains a receptor binding domain (RBD) that can specifically bind to angiotensin-converting enzyme 2 (ACE2), the receptor on target cells. Triggered by receptor binding, proteolytic processing and/or acidic pH in the cellular compartments, the class I viral fusion protein undergoes a transition from a metastable pre-fusion state to a stable post-fusion state during infection, in which the receptor-binding subunit is cleaved, and the fusion subunit undergoes large-scale conformational rearrangements to expose the hydrophobic fusion peptide, induce the formation of a six-helix bundle, and bring the viral and cellular membranes close for fusion. The trimeric SARS coronavirus (SARS-CoV-2) S glycoprotein consisting of three S1-S2 heterodimers binds the cellular receptor angiotensin-converting enzyme 2 (ACE2) and mediates fusion of the viral and cellular membranes through a pre- to post-fusion conformation transition. The emergence of the B.1.1.7 variant of SARS-CoV-2, also known as the variant of concern (VOC) 202012/01 strain, was first identified in the United Kingdom (UK) in 2020. Additionally, the B.1.1.7 was significantly more transmissible than other preexisting variants. The B.1.1.7 variant contains a significant mutation of interest in the RBD, the asparagine (N) to tyrosine (Y) mutation at position 501 (N501Y), which has been shown to result in enhanced binding affinity for hACE-2.