LysePred: A Multiscale Convolutional Neural Network for Predicting Hemolytic Activity of Antimicrobial Peptides

IF 4.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2026-07-17 Epub Date: 2026-06-24 DOI:10.1021/acssynbio.6c00173
Changhang Lin, Jinjin Li, Chen Su, Shuwen Xiong, Xiaorui Kang, Junwen Lu and Leyi Wei*, 
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引用次数: 0

Abstract

Antimicrobial peptides (AMPs) represent promising alternatives to conventional antibiotics, yet hemolytic toxicity remains a critical barrier to clinical translation, with approximately 70% of known AMPs exhibiting high or moderate hemolytic activity. Existing computational prediction methods are often constrained by deficiencies, including high computational complexities, the inability to capture multiscale sequence patterns, and insufficient generalization across diverse datasets. We present LysePred, a multiscale convolutional neural network to address these deficiencies concurrently by employing parallel branches with exponentially spaced kernel sizes to simultaneously capture local amino acid motifs (bigrams, 4-g) and longer-range amphipathic patterns (8- to 32-g). LysePred achieves top-tier performance on six benchmark datasets, exceeding the performance of the second-best method by 9.13% in MCC and 3.65% in ACC on average, while maintaining exceptional stability (MCC CV < 6.92%, ACC CV < 2.73%). Furthermore, independent validation on the HemoPI2 dataset demonstrates that LysePred delivers highly competitive results with a computationally parsimonious design (∼0.55 M parameters). This represents a reduction in parameter density of 1 to 2 orders of magnitude compared to Transformer-based approaches, such as the 8M-parameter ESM-2 or the 110M-parameter BERT Base while maintaining linear complexity for high-throughput screening. Ablation studies validate that the multiscale architecture contributes meaningfully to performance, with single-scale variants showing up to 13.35% MCC degradation. Interpretability analyses via t-SNE visualization and SHAP feature importance reveal that LysePred learns biologically meaningful representations integrating both local sequence motifs and global structural patterns. LysePred offers a practical, efficient, and interpretable tool for rapid hemolytic toxicity prediction in antimicrobial peptide development. Code and data are available at https://github.com/lincubator/LysePred.

Abstract Image

用于预测抗菌肽溶血活性的多尺度卷积神经网络。
抗菌肽(AMPs)是传统抗生素的有希望的替代品,但溶血毒性仍然是临床转化的关键障碍,大约70%的已知AMPs具有高或中度溶血活性。现有的计算预测方法经常受到缺陷的限制,包括高计算复杂性,无法捕获多尺度序列模式,以及对不同数据集的泛化不足。我们提出了LysePred,这是一个多尺度卷积神经网络,通过使用具有指数间隔核大小的平行分支来同时捕获局部氨基酸基序(biggram, 4-g)和更长距离的两偶模式(8- 32-g)来解决这些缺陷。LysePred在6个基准数据集上实现了顶级性能,在MCC和ACC方面的平均性能分别比第二优方法高出9.13%和3.65%,同时保持了优异的稳定性(MCC CV < 6.92%, ACC CV < 2.73%)。此外,在HemoPI2数据集上的独立验证表明,LysePred以计算简约的设计(约0.55 M参数)提供了极具竞争力的结果。与基于变压器的方法(如8m参数的ESM-2或110m参数的BERT Base)相比,这意味着参数密度降低了1到2个数量级,同时保持了高通量筛选的线性复杂性。消融研究证实,多尺度架构对性能有重大贡献,单尺度变体显示高达13.35%的MCC退化。通过t-SNE可视化和SHAP特征重要性的可解释性分析表明,LysePred学习了整合局部序列基序和全局结构模式的具有生物学意义的表征。LysePred为抗菌肽开发中的快速溶血毒性预测提供了一种实用、高效、可解释的工具。代码和数据可在https://github.com/lincubator/LysePred上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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