Development of new drugs is an expensive and time-consuming process. Due to the world-wide SARS-CoV-2 outbreak, it is essential that new drugs for SARS-CoV-2 are developed as soon as possible. Drug repurposing techniques can reduce the time span needed to develop new drugs by probing the list of existing FDA-approved drugs and their properties to reuse them for combating the new disease. We propose a novel architecture DeepGLSTM, which is a Graph Convolutional network and LSTM based method that predicts binding affinity values between the FDA-approved drugs and the viral proteins of SARS-CoV-2. Our proposed model has been trained on Davis, KIBA (Kinase Inhibitor Bioactivity), DTC (Drug Target Commons), Metz, ToxCast and STITCH datasets. We use our novel architecture to predict a Combined Score (calculated using Davis and KIBA score) of 2,304 FDA-approved drugs against 5 viral proteins. On the basis of the Combined Score, we prepare a list of the top-18 drugs with the highest binding affinity for 5 viral proteins present in SARS-CoV-2. Subsequently, this list may be used for the creation of new useful drugs.
翻译:开发新药物是一个昂贵和耗时的过程。由于全世界范围内的SARS-COV-2爆发,必须尽快开发SARS-COV-2的新药物。药物重新定位技术可以减少研制新药物所需的时间,方法是对现有的由FDA批准的药物清单及其特性进行勘查,以便重新使用这些药物来对付新疾病。我们建议建立一个新型结构DeepGLSTM,这是一个图表革命网络和以LSTM为基础的方法,预测FDA批准的药物与SA-COV-2的病毒蛋白质之间的结合值。我们提议的模型已经在Davis、KIBA(Kinase Inhibitor Biovicity)、DTC(药物目标公域)、Metz、ToxCast和STITCH数据集进行了培训。我们使用我们的新结构来预测在5种病毒蛋白质中2 304种药物(用Davis和KIBA分算出)由FDAFDAFDA批准的药物与5种病毒蛋白质的结合值。根据联合评分,我们编制了一份具有最高约束力的18种药物清单,用于目前5种病毒蛋白质试验。