计算机科学
水准点(测量)
理论(学习稳定性)
人工智能
集合(抽象数据类型)
机器学习
蛋白质工程
数据挖掘
优先次序
过程(计算)
特征(语言学)
回归
训练集
钥匙(锁)
蛋白质设计
深度学习
价值(数学)
酶动力学
计算生物学
光学(聚焦)
基质(水族馆)
监督学习
航程(航空)
特征选择
数据集
模式识别(心理学)
作者
Jianan Sui,Ran Xu,Hui Sun,Hongliang Duan,Liangzhen Zheng,Jingjing Guo
标识
DOI:10.1021/acs.jctc.6c00821
摘要
Accurately predicting the functional attributes of enzyme mutants is crucial for accelerating enzyme engineering and optimizing biocatalytic systems. Most existing methods focus on enzyme information or a limited set of properties while overlooking key interactions between enzyme mutants and their substrates. To address this limitation, we propose EZPro-Multi, a unified deep learning framework for predicting multiple biochemical properties, including catalytic efficiency ( k cat ), stability (ΔΔ G ), and solubility (Δ Sol ). EZPro-Multi integrates ProtT5-based protein representations with Molformer-based substrate representations through a cross-attention module to capture mutant–substrate interactions. The framework further incorporates supervised contrastive learning to improve feature discriminability by contrasting mutant–substrate pairs with similar or distinct catalytic changes measured on the same substrate. In addition, an auxiliary classification head is introduced to provide extra supervision and enhance the performance of the primary regression task. We evaluate EZPro-Multi using a curated k cat data set comprising diverse enzyme-substrate pairs, achieving state-of-the-art results. Comparative experiments show that EZPro-Multi outperforms existing methods in both regression accuracy and classification consistency. The framework also demonstrates promising performance in predicting ΔΔ G and Δ Sol across multiple benchmark data sets. Notably, on the deep mutational scanning (DMS) data set, integrating k cat, ΔΔ G, and Δ Sol significantly improves the hit rate for the top 10% high-activity mutants compared with single-property prediction, further highlighting the value of multi-property integration. Overall, EZPro-Multi provides a unified computational framework for multi-property assessment of enzyme variants and offers practical value for candidate prioritization in enzyme engineering.
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