AlphaFold2是否有助于提高单序列PPI位点预测的准确性?

Zhe Liu, Weihao Pan, Xu Zhen, Ji Liang, Wenxiang Cai, Kai Yuan, G. Lin
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引用次数: 0

摘要

AlphaFold2在蛋白质上实现了较高的结构预测精度。然而,据报道,直接将坐标输入深度学习模型并不能在下游任务上取得理想的结果。因此,如何将预测结果处理成深度学习网络能够理解的有效形式,以提高下游任务的性能是值得探索的。本研究以单序列PPI位点预测为例,验证了空间改变、SVD20和rASA特征计算三种坐标处理策略的效果。实验结果表明,空间滤波和rASA特征是深度学习模型结构信息编码的两种有效且合适的方法。此外,我们还进行了一个突变蛋白的案例研究。结果证明,当蛋白质突变发生时,空间滤波可能会潜在地引入HHblits谱和深度学习网络的结构变化。这项工作为下游任务提供了新的见解,例如预测蛋白质的结合位点或预测突变的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Will AlphaFold2 Be Helpful in Improving the Accuracy of Single-sequence PPI Site Prediction?
AlphaFold2 has achieved relatively high structure prediction accuracy on proteins. However, it is reported that directly feeding coordinates into deep learning models cannot achieve ideal results on downstream tasks. Therefore, how to process the predicted results into an effective form that deep learning networks can understand to improve the performance of downstream tasks is worth exploring. In this study, taking single-sequence PPI site prediction as an example, we verified the effects of three processing strategies of coordinates, namely spatial Altering, SVD20, and the rASA feature calculation. The experiment results showed that spatial filtering and the rASA feature were two effective and suitable ways to encode structural information for deep learning models. Besides, we also performed a case study of a mutated protein. The results proved that spatial filtering might potentially introduce structural changes into HHblits profiles and deep learning networks when protein mutations occur. This work provides new insight into the downstream tasks, such as predicting the binding sites of proteins or predicting the effects of mutations.
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