School of Health, Medical and Applied Sciences, Central Queensland University, Bundaberg, Queensland 4670, Australia.
Institute for Glycomics, Griffith University, Southport, Queensland 4222, Australia.
Bioorg Med Chem. 2022 Oct 15;72:117003. doi: 10.1016/j.bmc.2022.117003. Epub 2022 Sep 9.
Prediction of protein-ligand binding affinities is crucial for computational drug discovery. A number of deep learning approaches have been developed in recent years to improve the accuracy of such affinity prediction. While the predicting power of these systems have advanced to some degrees depending on the dataset used for model training and testing, the effects of the quality and quantity of the underlying data have not been thoroughly examined. In this study, we employed erroneous datasets and data subsets of different sizes, created from one of the largest databases of experimental binding affinities, to train and evaluate a deep learning system based on convolutional neural networks. Our results show that data quality and quantity do have significant impacts on the prediction performance of trained models. Depending on the variations in data quality and quantity, the performance discrepancies could be comparable to or even larger than those observed among different deep learning approaches. In particular, the presence of proteins in the training data leads to a dramatic increase in prediction accuracy. This implies that continued accumulation of high-quality affinity data, especially for new protein targets, is indispensable for improving deep learning models to better predict protein-ligand binding affinities.
蛋白质 - 配体结合亲和力的预测对于计算药物发现至关重要。近年来,已经开发了许多深度学习方法来提高这种亲和力预测的准确性。虽然这些系统的预测能力已经根据用于模型训练和测试的数据集在一定程度上得到了提高,但基础数据的质量和数量的影响尚未得到彻底检查。在这项研究中,我们使用了来自最大的实验结合亲和力数据库之一的错误数据集和不同大小的数据子集来训练和评估基于卷积神经网络的深度学习系统。我们的结果表明,数据质量和数量确实对训练模型的预测性能有重大影响。根据数据质量和数量的变化,性能差异可能与不同深度学习方法之间观察到的差异相当,甚至更大。特别是,训练数据中存在蛋白质会导致预测准确性的显著提高。这意味着需要继续积累高质量的亲和力数据,特别是针对新的蛋白质靶标,这对于改进深度学习模型以更好地预测蛋白质 - 配体结合亲和力是必不可少的。