酶功能预测中的深度学习和新酶的发现

IF 4.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2026-10-16 Epub Date: 2026-09-04 DOI:10.1021/acssynbio.6c00633
Rongsheng Gao, Youmeng Liu, Chengye Duan, Nan Qin, Kunyu Liu, Tatsuhisa Tsuboi, Zhen Chen
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引用次数: 0

摘要

基因组和宏基因组数据的快速增长造成了蛋白质序列发现和酶功能表征之间的巨大差距。深度学习已经成为酶相关预测任务的重要工具,包括EC和GO注释、底物特异性、催化残留物鉴定、动力学参数估计、热稳定性、pH最优和候选物发现。这篇综述总结了最近的进展,重点是基准设计,而不仅仅是报告分数。我们通过输入方式、训练数据、分割策略、泄漏控制、评估度量和验证证据来比较有代表性的方法。在各个任务中,明显的性能提升可能来自数据集规模、注释质量、同源重叠、负采样或端点定义,而不仅仅是体系结构。目前的模型对于注释和候选优先级排序是有价值的,但是对于远程同源物、稀有功能或新的催化活性的强大发现仍然需要低身份或分布外的评估和实验验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Learning in Enzyme Function Prediction and Novel Enzyme Discovery

The rapid growth of genomic and metagenomic data has created a large gap between protein sequence discovery and enzyme functional characterization. Deep learning has become an important tool for enzyme-related prediction tasks, including EC and GO annotation, substrate specificity, catalytic-residue identification, kinetic-parameter estimation, thermostability, pH optima, and candidate discovery. This review summarizes recent progress with an emphasis on benchmark design rather than reported scores alone. We compare representative methods by input modality, training data, split strategy, leakage control, evaluation metric, and validation evidence. Across tasks, apparent performance gains can arise from dataset scale, annotation quality, homolog overlap, negative sampling, or endpoint definition rather than architecture alone. Current models are valuable for annotation and candidate prioritization, but robust discovery of remote homologs, rare functions, or new catalytic activities still requires low-identity or out-of-distribution evaluation and experimental validation.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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