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7B62

Crystal structure of SARS-CoV-2 spike protein N-terminal domain in complex with biliverdin

7B62 の概要
エントリーDOI10.2210/pdb7b62/pdb
分子名称Spike glycoprotein, BILIVERDINE IX ALPHA, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (8 entities in total)
機能のキーワードsarscov2, covid19, biliverdin, coronavirus, ntd, green, spike, glycoprotein, s1, viral protein
由来する生物種Severe acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2)
タンパク質・核酸の鎖数1
化学式量合計39920.94
構造登録者
Pye, V.E.,Rosa, A.,Roustan, C.,Cherepanov, P. (登録日: 2020-12-07, 公開日: 2021-04-28, 最終更新日: 2024-01-31)
主引用文献Rosa, A.,Pye, V.E.,Graham, C.,Muir, L.,Seow, J.,Ng, K.W.,Cook, N.J.,Rees-Spear, C.,Parker, E.,Dos Santos, M.S.,Rosadas, C.,Susana, A.,Rhys, H.,Nans, A.,Masino, L.,Roustan, C.,Christodoulou, E.,Ulferts, R.,Wrobel, A.G.,Short, C.E.,Fertleman, M.,Sanders, R.W.,Heaney, J.,Spyer, M.,Kjaer, S.,Riddell, A.,Malim, M.H.,Beale, R.,MacRae, J.I.,Taylor, G.P.,Nastouli, E.,van Gils, M.J.,Rosenthal, P.B.,Pizzato, M.,McClure, M.O.,Tedder, R.S.,Kassiotis, G.,McCoy, L.E.,Doores, K.J.,Cherepanov, P.
SARS-CoV-2 can recruit a heme metabolite to evade antibody immunity.
Sci Adv, 7:-, 2021
Cited by
PubMed Abstract: The coronaviral spike is the dominant viral antigen and the target of neutralizing antibodies. We show that SARS-CoV-2 spike binds biliverdin and bilirubin, the tetrapyrrole products of heme metabolism, with nanomolar affinity. Using cryo-electron microscopy and x-ray crystallography, we mapped the tetrapyrrole interaction pocket to a deep cleft on the spike N-terminal domain (NTD). At physiological concentrations, biliverdin significantly dampened the reactivity of SARS-CoV-2 spike with immune sera and inhibited a subset of neutralizing antibodies. Access to the tetrapyrrole-sensitive epitope is gated by a flexible loop on the distal face of the NTD. Accompanied by profound conformational changes in the NTD, antibody binding requires relocation of the gating loop, which folds into the cleft vacated by the metabolite. Our results indicate that SARS-CoV-2 spike NTD harbors a dominant epitope, access to which can be controlled by an allosteric mechanism that is regulated through recruitment of a metabolite.
PubMed: 33888467
DOI: 10.1126/sciadv.abg7607
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.82 Å)
構造検証レポート
Validation report summary of 7b62
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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