Hao Yixuan, Chen Maozi, Othman Yasmin, Xie Xiang-Qun, Feng Zhiwei
Department of Pharmaceutical Sciences and Computational Chemical Genomics Screening Center, School of Pharmacy; National Center of Excellence for Computational Drug Abuse Research; Drug Discovery Institute; Departments of Computational Biology and Structural Biology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
ACS Omega. 2022 Oct 10;7(42):37476-37484. doi: 10.1021/acsomega.2c04258. eCollection 2022 Oct 25.
Transmissible and infectious viruses can cause large-scale epidemics around the world. This is because the virus can constantly mutate and produce different variants and subvariants to counter existing treatments. Therefore, a variety of treatments are urgently needed to keep up with the mutation of the viruses. To facilitate the research of such treatment, we updated our Virus-CKB 1.0 to Virus-CKB 2.0, which contains 10 kinds of viruses, including enterovirus, dengue virus, hepatitis C virus, Zika virus, herpes simplex virus, , human immunodeficiency virus, Ebola virus, Lassa virus, influenza virus, coronavirus, and norovirus. To date, Virus-CKB 2.0 archived at least 65 antiviral drugs (such as remdesivir, telaprevir, acyclovir, boceprevir, and nelfinavir) in the market, 178 viral-related targets with 292 available 3D crystal or cryo-EM structures, and 3766 chemical agents reported for these target proteins. Virus-CKB 2.0 is integrated with established tools for target prediction and result visualization; these include HTDocking, TargetHunter, blood-brain barrier (BBB) predictor, Spider Plot, etc. The Virus-CKB 2.0 server is accessible at https://www.cbligand.org/g/virus-ckb. By using the established chemogenomic tools and algorithms and newly developed tools, we can screen FDA-approved drugs and chemical compounds that may bind to these proteins involved in viral-associated disease regulation. If the virus strain mutates and the vaccine loses its effect, we can still screen drugs that can be used to treat the mutated virus in a fleeting time. In some cases, we can even repurpose FDA-approved drugs through Virus-CKB 2.0.
可传播和感染性病毒可在全球引发大规模疫情。这是因为该病毒会不断变异,产生不同的变种和亚变种以对抗现有的治疗方法。因此,迫切需要多种治疗方法来跟上病毒的变异。为促进此类治疗的研究,我们将病毒-化合物知识库1.0更新为病毒-化合物知识库2.0,其中包含10种病毒,包括肠道病毒、登革热病毒、丙型肝炎病毒、寨卡病毒、单纯疱疹病毒、人类免疫缺陷病毒、埃博拉病毒、拉沙热病毒、流感病毒、冠状病毒和诺如病毒。截至目前,病毒-化合物知识库2.0已收录了市场上至少65种抗病毒药物(如瑞德西韦、特拉匹韦、阿昔洛韦、波普瑞韦和奈非那韦)、178个病毒相关靶点以及292个可用的3D晶体或冷冻电镜结构,还有3766种针对这些靶蛋白报道的化学试剂。病毒-化合物知识库2.0集成了用于靶点预测和结果可视化的成熟工具;这些工具包括HTDocking、TargetHunter、血脑屏障(BBB)预测器、蜘蛛图等。可通过https://www.cbligand.org/g/virus-ckb访问病毒-化合物知识库2.0服务器。通过使用已建立的化学基因组学工具和算法以及新开发的工具,我们可以筛选出可能与这些参与病毒相关疾病调节的蛋白质结合的FDA批准药物和化合物。如果病毒株发生变异且疫苗失效,我们仍可在短时间内筛选出可用于治疗变异病毒的药物。在某些情况下,我们甚至可以通过病毒-化合物知识库2.0重新利用FDA批准的药物。