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7EDJ

Cryo-EM structure of SARS-CoV-2 S-UK variant (B.1.1.7) in complex with Angiotensin-converting enzyme 2 (ACE2) ectodomain

Summary for 7EDJ
Entry DOI10.2210/pdb7edj/pdb
Related7EDF 7EDG 7EDH 7EDI
EMDB information31069 31070 31071 31072 31073
DescriptorSpike glycoprotein, Angiotensin-converting enzyme 2 (ACE2) ectodomain, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
Functional Keywordssars-cov-2, spike protein, viral protein
Biological sourceSevere acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
More
Total number of polymer chains6
Total formula weight740867.86
Authors
Yang, T.J.,Yu, P.Y.,Chang, Y.C.,Wu, H.C.,Hsu, S.T.D. (deposition date: 2021-03-16, release date: 2021-09-01, Last modification date: 2024-10-16)
Primary citationYang, T.J.,Yu, P.Y.,Chang, Y.C.,Liang, K.H.,Tso, H.C.,Ho, M.R.,Chen, W.Y.,Lin, H.T.,Wu, H.C.,Hsu, S.D.
Effect of SARS-CoV-2 B.1.1.7 mutations on spike protein structure and function.
Nat.Struct.Mol.Biol., 28:731-739, 2021
Cited by
PubMed Abstract: The B.1.1.7 variant of SARS-CoV-2 first detected in the UK harbors amino-acid substitutions and deletions in the spike protein that potentially enhance host angiotensin conversion enzyme 2 (ACE2) receptor binding and viral immune evasion. Here we report cryo-EM structures of the spike protein of B.1.1.7 in the apo and ACE2-bound forms. The apo form showed one or two receptor-binding domains (RBDs) in the open conformation, without populating the fully closed state. All three RBDs were engaged in ACE2 binding. The B.1.1.7-specific A570D mutation introduces a molecular switch that could modulate the opening and closing of the RBD. The N501Y mutation introduces a π-π interaction that enhances RBD binding to ACE2 and abolishes binding of a potent neutralizing antibody (nAb). Cryo-EM also revealed how a cocktail of two nAbs simultaneously bind to all three RBDs, and demonstrated the potency of the nAb cocktail to neutralize different SARS-CoV-2 pseudovirus strains, including B.1.1.7.
PubMed: 34385690
DOI: 10.1038/s41594-021-00652-z
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.3 Å)
Structure validation

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