利用alphafold2预测结构和表面特征进行抗菌肽鉴定的多模态几何学习。

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Zehua Sun, Jing Xu, Yumeng Zhang, Yiwen Zhang, Zhikang Wang, Xiaoyu Wang, Shanshan Li, Yuming Guo, Hsin Hui Shen, Jiangning Song
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引用次数: 0

摘要

抗菌肽(Antimicrobial peptides, AMPs)是一种短肽,在多种生物过程中发挥重要作用,并表现出对目标生物的功能活性。虽然许多方法已经证明了使用序列特征进行AMP识别的深度神经网络的有效性;然而,更高层次的肽特征,如三维结构和几何表面特征,尚未得到全面的探索。为了解决这一差距,我们引入了ssfgm模型(序列、结构、表面、图形和基于几何的模型),这是一个集成了多种特征类型以增强AMP识别的新框架。该模型将每个肽序列表示为一个图,其中节点的特征是来自ProteinBERT、ESM-2和One-hot嵌入的氨基酸特征。图卷积网络和注意机制用于捕获高阶结构和顺序关系。此外,使用几何神经网络处理表面几何和物理化学性质。最后,一个特征融合策略结合了这些子网的输出,以实现鲁棒的AMP识别。广泛的基准测试实验表明,ssfgm模型优于当前最先进的方法。一项消融研究进一步证实了序列、结构和表面特征在AMP鉴定中的关键作用。这项工作的关键贡献是对多肽特征的多层次创新整合以及几何和图形神经网络的结合。该方法可以更全面地了解肽的序列-结构-功能关系,为更准确地预测AMP铺平道路。ssfgm模型在发现和设计新的基于amp的治疗方法方面具有重要的应用潜力。源代码可在https://github.com/ggcameronnogg/SSFGM-Model上公开获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal geometric learning for antimicrobial peptide identification by leveraging alphafold2-predicted structures and surface features.

Antimicrobial peptides (AMPs) are short peptides that play critical roles in diverse biological processes and exhibit functional activities against target organisms. While numerous methods have demonstrated the effectiveness of deep neural networks for AMP identification using sequence features; nevertheless, higher-level peptide characteristics-such as 3D structure and geometric surface features-have not been comprehensively explored. To address this gap, we introduce the SSFGM-Model (Sequence, Structure, Surface, Graph, and Geometric-based Model), a novel framework that integrates multiple feature types to enhance AMP identification. The model represents each peptide sequence as a graph, where nodes are characterized by amino acid features derived from ProteinBERT, ESM-2, and One-hot embeddings. Graph convolutional networks and an attention mechanism are employed to capture high-order structural and sequential relationships. Additionally, surface geometry and physicochemical properties are processed using a geometric neural network. Finally, a feature fusion strategy combines the outputs from these subnetworks to enable robust AMP identification. Extensive benchmarking experiments demonstrate that the SSFGM-Model outperforms current state-of-the-art methods. An ablation study further confirms the critical role of sequence, structural, and surface features in AMP identification. The key contribution of this work is the innovative integration of multiple levels of peptide characteristics and the combination of geometric and graph neural networks. This approach provides a more comprehensive understanding of the sequence-structure-function relationship of peptides, paving the way for more accurate AMP prediction. The SSFGM-Model has a significant potential for applications in the discovery and design of novel AMP-based therapeutics. The source code is publicly available at https://github.com/ggcameronnogg/SSFGM-Model.

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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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