Syifa Zahara Kultsum Azmi, S. Sunarno, Sinta Aulia Rahmah, Melisa Andriani, Azlya Reza Lailul Farobi, Luke Nur Ahlina
{"title":"Utilization of Quercetin Flavonoid Compounds in Red Onion (Allium cepa L.) as Inhibitor of Spike Sars-CoV-2 Protein against ACE2 Receptors","authors":"Syifa Zahara Kultsum Azmi, S. Sunarno, Sinta Aulia Rahmah, Melisa Andriani, Azlya Reza Lailul Farobi, Luke Nur Ahlina","doi":"10.15294/biosaintifika.v13i3.32027","DOIUrl":null,"url":null,"abstract":"The world is facing the challenge of the COVID-19 disease, which is now stated as a pandemic. Inside the host cell, spike envelope protein (spike) of SARS-CoV-2 interact with the Angiotensin-converting Enzyme 2 (ACE2) receptor. It can be inhibited by bioactive compounds such as flavonoids which have anti-viral and broad pharmacological effect. This study aimed to determine the spike protein inhibitory activity by quercetin against the ACE2 receptor using the molecular docking method. This study focused on the inhibitory of the penetration activity of s proteins in ACE2 by utilizing natural material compounds that have the potential to be used as anti-SARS-CoV-2 drug development agents. The flavonoid compound quercetin was extracted by the maceration method. The quantitative analysis was carried out using a UV-Vis spectrophotometer to prove the presence of quercetin content. Molecular docking simulations were carried out to look for the binding affinity between the spike protein and quercetin. Docking was carried out using the Autodock, PyRx, and visualization using Discovery Studio. Indicators that prove that quercetin forms binding affinity and protein complexes with spikes are the Vina Score and RMSD. It is also supported by ADME analysis and conformity to Lipinski's rules of five. That matter becomes a success indicator of the spike activity inhibition by quercetin, which makes it possible to be used as an anti-SARS-CoV-2 drug development agent. The novelty from this study is molecular docking method that used to show that quercetin in red onion had inhibitory activity on the penetration process of protein spike in SARS-CoV-2. Results obtained from this study can be used as a recommendation for advanced research in invitro and invivo studies as a drug which has potential to inhibit protein spike of SARSCoV-2. [ FROM AUTHOR] Copyright of Biosaintifika: Journal of Biology & Biology Education is the property of Jurusan Biologi, Fakultas Matematika dan Ilmu Pengetahuan Universitas Negeri Semarang and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)","PeriodicalId":30622,"journal":{"name":"Biosaintifika Journal of Biology Biology Education","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosaintifika Journal of Biology Biology Education","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15294/biosaintifika.v13i3.32027","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
The world is facing the challenge of the COVID-19 disease, which is now stated as a pandemic. Inside the host cell, spike envelope protein (spike) of SARS-CoV-2 interact with the Angiotensin-converting Enzyme 2 (ACE2) receptor. It can be inhibited by bioactive compounds such as flavonoids which have anti-viral and broad pharmacological effect. This study aimed to determine the spike protein inhibitory activity by quercetin against the ACE2 receptor using the molecular docking method. This study focused on the inhibitory of the penetration activity of s proteins in ACE2 by utilizing natural material compounds that have the potential to be used as anti-SARS-CoV-2 drug development agents. The flavonoid compound quercetin was extracted by the maceration method. The quantitative analysis was carried out using a UV-Vis spectrophotometer to prove the presence of quercetin content. Molecular docking simulations were carried out to look for the binding affinity between the spike protein and quercetin. Docking was carried out using the Autodock, PyRx, and visualization using Discovery Studio. Indicators that prove that quercetin forms binding affinity and protein complexes with spikes are the Vina Score and RMSD. It is also supported by ADME analysis and conformity to Lipinski's rules of five. That matter becomes a success indicator of the spike activity inhibition by quercetin, which makes it possible to be used as an anti-SARS-CoV-2 drug development agent. The novelty from this study is molecular docking method that used to show that quercetin in red onion had inhibitory activity on the penetration process of protein spike in SARS-CoV-2. Results obtained from this study can be used as a recommendation for advanced research in invitro and invivo studies as a drug which has potential to inhibit protein spike of SARSCoV-2. [ FROM AUTHOR] Copyright of Biosaintifika: Journal of Biology & Biology Education is the property of Jurusan Biologi, Fakultas Matematika dan Ilmu Pengetahuan Universitas Negeri Semarang and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)
世界正面临COVID-19疾病的挑战,该疾病现已被宣布为大流行。在宿主细胞内,SARS-CoV-2的穗包膜蛋白(spike)与血管紧张素转换酶2 (ACE2)受体相互作用。黄酮类化合物等具有抗病毒和广泛药理作用的生物活性化合物可抑制其生长。本研究旨在利用分子对接法测定槲皮素对ACE2受体刺突蛋白的抑制活性。本研究的重点是利用可能用作抗sars - cov -2药物开发剂的天然材料化合物抑制ACE2中s蛋白的渗透活性。采用浸渍法提取黄酮类化合物槲皮素。用紫外可见分光光度计进行定量分析,证实槲皮素的存在。进行分子对接模拟,寻找刺突蛋白与槲皮素之间的结合亲和力。对接使用Autodock, PyRx,并使用Discovery Studio进行可视化。证明槲皮素与尖刺形成结合亲和力和蛋白复合物的指标是Vina Score和RMSD。这也得到了ADME分析的支持,并符合Lipinski的五个规则。该物质成为槲皮素抑制刺突活性的成功指标,这使其有可能用作抗sars - cov -2药物开发剂。本研究的新颖之处在于分子对接方法,该方法证明了红洋葱中的槲皮素对SARS-CoV-2蛋白刺突穿透过程具有抑制作用。本研究结果可作为一种有抑制SARSCoV-2蛋白尖峰潜力的药物,用于体外和体内研究的进一步研究。《生物与生物教育杂志》是Jurusan Biologi, Fakultas Matematika dan Ilmu Pengetahuan Universitas Negeri三宝朗的财产,未经版权所有者的明确书面许可,其内容不得复制或通过电子邮件发送到多个网站或发布到listserv。但是,用户可以打印、下载或通过电子邮件发送文章供个人使用。这可以删节。对副本的准确性不作任何保证。用户应参阅原始出版版本的材料的完整。(版权适用于所有人。)