计算机科学
人工智能
序列(生物学)
深度学习
一般化
模式识别(心理学)
卷积神经网络
交互信息
代表(政治)
人工神经网络
特征(语言学)
蛋白质-蛋白质相互作用
感知器
钥匙(锁)
机器学习
特征选择
结合位点
构造(python库)
多层感知器
蛋白质测序
数据挖掘
相互作用模型
生物系统
特征学习
特征提取
交互网络
接口(物质)
序列学习
蛋白质结构
算法
作者
Xinyi Xu,Haotian Zhang,Qi Liu,Qian Cheng,Yingying Guo,Yang Wei,Xueli Chen
标识
DOI:10.1021/acs.jcim.5c01734
摘要
Quantitative prediction of binding affinity in protein-protein interactions is critical for deciphering biological mechanisms and advancing therapeutic antibody development. While experimental methods for measuring binding affinity remain limited by high-cost, low-throughput constraints, deep learning offers a promising alternative. This study proposes SSIF-affinity, an innovative multimodal deep learning framework that enables high-precision prediction of protein-protein complex binding affinity. First, this method innovatively locates the binding interface and constructs a geometrically constrained binding region, screening key atoms and residues within the binding region. Construct structural diagram data for the selected key atoms to extract atomic-level protein complex interaction features. Second, through the structure-guided cross modal attention module, the structural and sequence features of the selected key residues are fused to capture the structural interactions between residues and the correlations between sequence evolutions. In addition, extracting features of full-length sequence information through convolutional neural network (CNN) and long short-term memory (LSTM) network not only captures local interaction features between sequences, but also mines long-range dependencies through temporal modeling. The final integrated multilevel feature input multilayer perceptron (MLP) regression module predicts the binding affinity values of protein-protein complexes. Specifically, the framework effectively reduces redundant calculations and noise interference by combining region selection strategies and overcomes the limitations of the unimodal approach that only uses sequence or structural information through a collaborative representation mechanism of the full-length sequence features of protein complexes and the structural features within the binding region, effectively balancing the contributions of interface interactions and long-range interactions. The case studies on antibody-antigen complexes further validate the model's generalization ability. SSIF-affinity provides a new strategy for predicting binding affinity in protein-protein complexes, offering a new paradigm for AI-driven antibody drug discovery.
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