mACPpred 2.0:利用集成空间和概率特征表征的堆叠深度学习进行抗癌肽预测

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

抗癌肽(ACPs)是天然存在的分子,具有靶向和杀死癌细胞的巨大潜力。然而,仅根据主要氨基酸序列来识别抗癌肽仍然是免疫信息学的一大障碍。过去,人们提出了一些基于网络的机器学习(ML)工具,以帮助研究人员识别潜在的 ACPs,并进行进一步测试。值得注意的是,我们在 2019 年推出的元方法 mACPpred 极大地推动了 ACP 研究领域的发展。鉴于表征 ACP 的数量呈指数级增长,现在迫切需要创建 mACPpred 的更新版本。为了开发 mACPpred 2.0,我们整合了所有公开的 ACP 数据集,构建了一个最新的基准数据集。我们采用了大规模的特征描述器,包括传统的特征描述器和基于自然语言处理(NLP)的高级预训练嵌入。我们使用 11 种不同的分类器评估了它们区分 ACP 和非 ACP 的能力。随后,我们采用了叠加深度学习(SDL)方法,将一维卷积神经网络(1D CNN)块和混合特征结合在一起。这些特征包括基于 NLP 的前七种表现特征和 90 种概率特征,使我们能够识别这些不同特征中隐藏的模式,提高 ACP 预测模型的准确性。这是第一项整合空间和概率特征表征来预测 ACP 的研究。严格的交叉验证和独立测试最终证明,mACPpred 2.0 不仅超越了其前身(mACPpred),而且还优于现有的最先进预测器,这凸显了通过 SDL 获得的高级特征表示能力的重要性。为了便于广泛使用和访问,我们为 mACPpred 2.0 开发了用户友好型网站 https://balalab-skku.org/mACPpred2/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

mACPpred 2.0: Stacked Deep Learning for Anticancer Peptide Prediction with Integrated Spatial and Probabilistic Feature Representations

mACPpred 2.0: Stacked Deep Learning for Anticancer Peptide Prediction with Integrated Spatial and Probabilistic Feature Representations

Anticancer peptides (ACPs), naturally occurring molecules with remarkable potential to target and kill cancer cells. However, identifying ACPs based solely from their primary amino acid sequences remains a major hurdle in immunoinformatics. In the past, several web-based machine learning (ML) tools have been proposed to assist researchers in identifying potential ACPs for further testing. Notably, our meta-approach method, mACPpred, introduced in 2019, has significantly advanced the field of ACP research. Given the exponential growth in the number of characterized ACPs, there is now a pressing need to create an updated version of mACPpred. To develop mACPpred 2.0, we constructed an up-to-date benchmarking dataset by integrating all publicly available ACP datasets. We employed a large-scale of feature descriptors, encompassing both conventional feature descriptors and advanced pre-trained natural language processing (NLP)-based embeddings. We evaluated their ability to discriminate between ACPs and non-ACPs using eleven different classifiers. Subsequently, we employed a stacked deep learning (SDL) approach, incorporating 1D convolutional neural network (1D CNN) blocks and hybrid features. These features included the top seven performing NLP-based features and 90 probabilistic features, allowing us to identify hidden patterns within these diverse features and improve the accuracy of our ACP prediction model. This is the first study to integrate spatial and probabilistic feature representations for predicting ACPs. Rigorous cross-validation and independent tests conclusively demonstrated that mACPpred 2.0 not only surpassed its predecessor (mACPpred) but also outperformed the existing state-of-the-art predictors, highlighting the importance of advanced feature representation capabilities attained through SDL. To facilitate widespread use and accessibility, we have developed a user-friendly for mACPpred 2.0, available at https://balalab-skku.org/mACPpred2/.

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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