Automatic generation of functional peptides with desired bioactivity and membrane permeability using Bayesian optimization.

IF 2.8 4区 医学 Q3 CHEMISTRY, MEDICINAL
Molecular Informatics Pub Date : 2024-04-01 Epub Date: 2024-02-19 DOI:10.1002/minf.202300148
Itsuki Fukunaga, Yuki Matsukiyo, Kazuma Kaitoh, Yoshihiro Yamanishi
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引用次数: 0

Abstract

Peptides are potentially useful modalities of drugs; however, cell membrane permeability is an obstacle in peptide drug discovery. The identification of bioactive peptides for a therapeutic target is also challenging because of the huge amino acid sequence patterns of peptides. In this study, we propose a novel computational method, PEptide generation system using Neural network Trained on Amino acid sequence data and Gaussian process-based optimizatiON (PENTAGON), to automatically generate new peptides with desired bioactivity and cell membrane permeability. In the algorithm, we mapped peptide amino acid sequences onto the latent space constructed using a variational autoencoder and searched for peptides with desired bioactivity and cell membrane permeability using Bayesian optimization. We used our proposed method to generate peptides with cell membrane permeability and bioactivity for each of the nine therapeutic targets, such as the estrogen receptor (ER). Our proposed method outperformed a previously developed peptide generator in terms of similarity to known active peptide sequences and the length of generated peptide sequences.

利用贝叶斯优化技术自动生成具有所需生物活性和膜渗透性的功能肽。
肽是一种潜在的有用药物;然而,细胞膜渗透性是肽药物发现的一个障碍。由于肽的氨基酸序列模式庞大,识别治疗靶点的生物活性肽也具有挑战性。在这项研究中,我们提出了一种新的计算方法--基于氨基酸序列数据和高斯过程优化训练的神经网络多肽生成系统(PENTAGON),用于自动生成具有所需生物活性和细胞膜渗透性的新多肽。在该算法中,我们将多肽氨基酸序列映射到使用变异自动编码器构建的潜空间上,并使用贝叶斯优化法搜索具有所需生物活性和细胞膜渗透性的多肽。我们使用所提出的方法为雌激素受体(ER)等九个治疗靶点生成了具有细胞膜渗透性和生物活性的多肽。就与已知活性肽序列的相似性和生成肽序列的长度而言,我们提出的方法优于之前开发的肽生成器。
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
Molecular Informatics
Molecular Informatics CHEMISTRY, MEDICINAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.30
自引率
2.80%
发文量
70
审稿时长
3 months
期刊介绍: Molecular Informatics is a peer-reviewed, international forum for publication of high-quality, interdisciplinary research on all molecular aspects of bio/cheminformatics and computer-assisted molecular design. Molecular Informatics succeeded QSAR & Combinatorial Science in 2010. Molecular Informatics presents methodological innovations that will lead to a deeper understanding of ligand-receptor interactions, macromolecular complexes, molecular networks, design concepts and processes that demonstrate how ideas and design concepts lead to molecules with a desired structure or function, preferably including experimental validation. The journal''s scope includes but is not limited to the fields of drug discovery and chemical biology, protein and nucleic acid engineering and design, the design of nanomolecular structures, strategies for modeling of macromolecular assemblies, molecular networks and systems, pharmaco- and chemogenomics, computer-assisted screening strategies, as well as novel technologies for the de novo design of biologically active molecules. As a unique feature Molecular Informatics publishes so-called "Methods Corner" review-type articles which feature important technological concepts and advances within the scope of the journal.
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