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-Structure paper
タイトル | ACE2-targeting monoclonal antibody as potent and broad-spectrum coronavirus blocker. |
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ジャーナル・号・ページ | Signal Transduct Target Ther, Vol. 6, Issue 1, Page 315, Year 2021 |
掲載日 | 2021年8月25日 |
![]() | Yuning Chen / Ya-Nan Zhang / Renhong Yan / Guifeng Wang / Yuanyuan Zhang / Zhe-Rui Zhang / Yaning Li / Jianxia Ou / Wendi Chu / Zhijuan Liang / Yongmei Wang / Yi-Li Chen / Ganjun Chen / Qi Wang / Qiang Zhou / Bo Zhang / Chunhe Wang / ![]() |
PubMed 要旨 | The evolution of coronaviruses, such as SARS-CoV-2, makes broad-spectrum coronavirus preventional or therapeutical strategies highly sought after. Here we report a human angiotensin-converting enzyme ...The evolution of coronaviruses, such as SARS-CoV-2, makes broad-spectrum coronavirus preventional or therapeutical strategies highly sought after. Here we report a human angiotensin-converting enzyme 2 (ACE2)-targeting monoclonal antibody, 3E8, blocked the S1-subunits and pseudo-typed virus constructs from multiple coronaviruses including SARS-CoV-2, SARS-CoV-2 mutant variants (SARS-CoV-2-D614G, B.1.1.7, B.1.351, B.1.617.1, and P.1), SARS-CoV and HCoV-NL63, without markedly affecting the physiological activities of ACE2 or causing severe toxicity in ACE2 "knock-in" mice. 3E8 also blocked live SARS-CoV-2 infection in vitro and in a prophylactic mouse model of COVID-19. Cryo-EM and "alanine walk" studies revealed the key binding residues on ACE2 interacting with the CDR3 domain of 3E8 heavy chain. Although full evaluation of safety in non-human primates is necessary before clinical development of 3E8, we provided a potentially potent and "broad-spectrum" management strategy against all coronaviruses that utilize ACE2 as entry receptors and disclosed an anti-coronavirus epitope on human ACE2. |
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手法 | EM (単粒子) |
解像度 | 3.2 - 3.4 Å |
構造データ | EMDB-31732, PDB-7v61: ![]() EMDB-31733: cryo-EM map focused on interface between 3E8 and ACE2 |
化合物 | ![]() ChemComp-NAG: ![]() ChemComp-ZN: ![]() ChemComp-HOH: |
由来 |
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![]() | MEMBRANE PROTEIN / ACE2-B0AT1 complex |