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深矿噬菌体裂解酶:从人类微生物组中深度挖掘噬菌体裂解酶。

DeepMineLys: Deep mining of phage lysins from human microbiome.

机构信息

School of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong 510006, China.

School of Biology and Biological Engineering, South China University of Technology, Guangzhou, Guangdong 510006, China.

出版信息

Cell Rep. 2024 Aug 27;43(8):114583. doi: 10.1016/j.celrep.2024.114583. Epub 2024 Aug 6.

Abstract

Vast shotgun metagenomics data remain an underutilized resource for novel enzymes. Artificial intelligence (AI) has increasingly been applied to protein mining, but its conventional performance evaluation is interpolative in nature, and these trained models often struggle to extrapolate effectively when challenged with unknown data. In this study, we present a framework (DeepMineLys [deep mining of phage lysins from human microbiome]) based on the convolutional neural network (CNN) to identify phage lysins from three human microbiome datasets. When validated with an independent dataset, our method achieved an F1-score of 84.00%, surpassing existing methods by 20.84%. We expressed 16 lysin candidates from the top 100 sequences in E. coli, confirming 11 as active. The best one displayed an activity 6.2-fold that of lysozyme derived from hen egg white, establishing it as the most potent lysin from the human microbiome. Our study also underscores several important issues when applying AI to biology questions. This framework should be applicable for mining other proteins.

摘要

大量的 shotgun 宏基因组学数据仍然是新型酶的未充分利用的资源。人工智能 (AI) 越来越多地应用于蛋白质挖掘,但它的常规性能评估本质上是插值的,并且这些经过训练的模型在遇到未知数据时往往难以有效地外推。在这项研究中,我们提出了一个基于卷积神经网络 (CNN) 的框架(DeepMineLys [从人类微生物组中挖掘噬菌体裂解酶]),用于从三个人类微生物组数据集识别噬菌体裂解酶。当用独立数据集进行验证时,我们的方法达到了 84.00%的 F1 得分,比现有方法高出 20.84%。我们在大肠杆菌中表达了前 100 个序列中的 16 个裂解酶候选物,证实其中 11 个具有活性。最好的一个显示出比来自鸡蛋白的溶菌酶高 6.2 倍的活性,使其成为来自人类微生物组的最有效裂解酶。我们的研究还强调了将 AI 应用于生物学问题时的几个重要问题。该框架应该适用于挖掘其他蛋白质。

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