tetano
Editor, Senior Moderator
J Transl Med
. 2022 Jul 14;20(1):314.
doi: 10.1186/s12967-022-03501-9.
Potential inhibitors for blocking the interaction of the coronavirus SARS-CoV-2 spike protein and its host cell receptor ACE2
Changzhi Li[SUP] #[/SUP][SUP] 1 2 [/SUP], Hongjuan Zhou[SUP] #[/SUP][SUP] 3 [/SUP], Lingling Guo[SUP] #[/SUP][SUP] 1 [/SUP], Dehuan Xie[SUP] 1 [/SUP], Huiping He[SUP] 1 4 [/SUP], Hong Zhang[SUP] 1 [/SUP], Yixiu Liu[SUP] 3 [/SUP], Lixia Peng[SUP] 1 [/SUP], Lisheng Zheng[SUP] 1 [/SUP], Wenhua Lu[SUP] 1 [/SUP], Yan Mei[SUP] 1 [/SUP], Zhijie Liu[SUP] 1 [/SUP], Jie Huang[SUP] 3 [/SUP], Mingdian Wang[SUP] 1 [/SUP], Ditian Shu[SUP] 1 [/SUP], Liuyan Ding[SUP] 1 [/SUP], Yanhong Lang[SUP] 1 [/SUP], Feifei Luo[SUP] 1 [/SUP], Jing Wang[SUP] 1 [/SUP], Bijun Huang[SUP] 1 [/SUP], Peng Huang[SUP] 1 [/SUP], Song Gao[SUP] 5 6 [/SUP], Jindong Chen[SUP] 7 [/SUP], Chao-Nan Qian[SUP] 8 9 10 [/SUP]
Affiliations
Abstract
Background: The outbreak of SARS-CoV-2 continues to pose a serious threat to human health and social. The ongoing pandemic of COVID-19 caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made a serious threat to public health and economic stability worldwide. Given the urgency of the situation, researchers are attempting to repurpose existing drugs for treating COVID-19.
Methods: We first established an anti-coronavirus drug screening platform based on the Homogeneous Time Resolved Fluorescence (HTRF) technology and the interaction between the coronavirus spike protein and its host receptor ACE2. Two compound libraries of 2,864 molecules were screened with this platform. Selected candidate compounds were validated by SARS-CoV-2_S pseudotyped lentivirus and ACE2-overexpressing cell system. Molecular docking was used to analyze the interaction between S protein and compounds.
Results: We identified three potential anti-coronavirus compounds: tannic acid (TA), TS-1276 (anthraquinone), and TS-984 (9-Methoxycanthin-6-one). Our in vitro validation experiments indicated that TS-984 strongly inhibits the interaction of the coronavirus S protein and the human cell ACE2 receptor. Additionally, tannic acid showed moderate inhibitory effect on the interaction of S protein and ACE2.
Conclusion: This platform is a rapid, sensitive, specific, and high throughput system, and available for screening large compound libraries. TS-984 is a potent blocker of the interaction between the S-protein and ACE2, which might have the potential to be developed into an effective anti-coronavirus drug.
Keywords: 9-Methoxycanthin-6-one; ACE2; COVID-19; Coronavirus; SARS-CoV-2; Spike protein; Tannic acid.
. 2022 Jul 14;20(1):314.
doi: 10.1186/s12967-022-03501-9.
Potential inhibitors for blocking the interaction of the coronavirus SARS-CoV-2 spike protein and its host cell receptor ACE2
Changzhi Li[SUP] #[/SUP][SUP] 1 2 [/SUP], Hongjuan Zhou[SUP] #[/SUP][SUP] 3 [/SUP], Lingling Guo[SUP] #[/SUP][SUP] 1 [/SUP], Dehuan Xie[SUP] 1 [/SUP], Huiping He[SUP] 1 4 [/SUP], Hong Zhang[SUP] 1 [/SUP], Yixiu Liu[SUP] 3 [/SUP], Lixia Peng[SUP] 1 [/SUP], Lisheng Zheng[SUP] 1 [/SUP], Wenhua Lu[SUP] 1 [/SUP], Yan Mei[SUP] 1 [/SUP], Zhijie Liu[SUP] 1 [/SUP], Jie Huang[SUP] 3 [/SUP], Mingdian Wang[SUP] 1 [/SUP], Ditian Shu[SUP] 1 [/SUP], Liuyan Ding[SUP] 1 [/SUP], Yanhong Lang[SUP] 1 [/SUP], Feifei Luo[SUP] 1 [/SUP], Jing Wang[SUP] 1 [/SUP], Bijun Huang[SUP] 1 [/SUP], Peng Huang[SUP] 1 [/SUP], Song Gao[SUP] 5 6 [/SUP], Jindong Chen[SUP] 7 [/SUP], Chao-Nan Qian[SUP] 8 9 10 [/SUP]
Affiliations
- PMID: 35836239
- DOI: 10.1186/s12967-022-03501-9
Abstract
Background: The outbreak of SARS-CoV-2 continues to pose a serious threat to human health and social. The ongoing pandemic of COVID-19 caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made a serious threat to public health and economic stability worldwide. Given the urgency of the situation, researchers are attempting to repurpose existing drugs for treating COVID-19.
Methods: We first established an anti-coronavirus drug screening platform based on the Homogeneous Time Resolved Fluorescence (HTRF) technology and the interaction between the coronavirus spike protein and its host receptor ACE2. Two compound libraries of 2,864 molecules were screened with this platform. Selected candidate compounds were validated by SARS-CoV-2_S pseudotyped lentivirus and ACE2-overexpressing cell system. Molecular docking was used to analyze the interaction between S protein and compounds.
Results: We identified three potential anti-coronavirus compounds: tannic acid (TA), TS-1276 (anthraquinone), and TS-984 (9-Methoxycanthin-6-one). Our in vitro validation experiments indicated that TS-984 strongly inhibits the interaction of the coronavirus S protein and the human cell ACE2 receptor. Additionally, tannic acid showed moderate inhibitory effect on the interaction of S protein and ACE2.
Conclusion: This platform is a rapid, sensitive, specific, and high throughput system, and available for screening large compound libraries. TS-984 is a potent blocker of the interaction between the S-protein and ACE2, which might have the potential to be developed into an effective anti-coronavirus drug.
Keywords: 9-Methoxycanthin-6-one; ACE2; COVID-19; Coronavirus; SARS-CoV-2; Spike protein; Tannic acid.