Enhancing Functional Protein Design Using Heuristic Optimization and Deep Learning for Anti-Inflammatory and Gene Therapy Applications.

IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Proteins-Structure Function and Bioinformatics Pub Date : 2025-07-01 Epub Date: 2025-02-22 DOI:10.1002/prot.26810
Ayşenur Soytürk Patat, Özkan Ufuk Nalbantoğlu
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引用次数: 0

Abstract

Protein sequence design is a highly challenging task, aimed at discovering new proteins that are more functional and producible under laboratory conditions than their natural counterparts. Deep learning-based approaches developed to address this problem have achieved significant success. However, these approaches often do not adequately emphasize the functional properties of proteins. In this study, we developed a heuristic optimization method to enhance key functionalities such as solubility, flexibility, and stability, while preserving the structural integrity of proteins. This method aims to reduce laboratory demands by enabling a design that is both functional and structurally sound. This approach is particularly valuable for the synthetic production of proteins with anti-inflammatory properties and those used in gene therapy. The designed proteins were initially evaluated for their ability to preserve natural structures using recovery and confidence metrics, followed by assessments with the AlphaFold tool. Additionally, natural protein sequences were mutated using a genetic algorithm and compared with those designed by our method. The results demonstrate that the protein sequences generated by our method exhibit much greater similarity to native protein sequences and structures. The code and sequences for the designed proteins are available at https://github.com/aysenursoyturk/HMHO.

利用启发式优化和深度学习增强抗炎和基因治疗应用的功能蛋白设计。
蛋白质序列设计是一项极具挑战性的任务,旨在发现在实验室条件下比其天然对应物更具功能和可生产性的新蛋白质。为解决这一问题而开发的基于深度学习的方法已经取得了重大成功。然而,这些方法往往没有充分强调蛋白质的功能特性。在这项研究中,我们开发了一种启发式优化方法来增强关键功能,如溶解度、灵活性和稳定性,同时保持蛋白质的结构完整性。这种方法旨在通过实现功能和结构健全的设计来减少实验室需求。这种方法对于合成具有抗炎特性的蛋白质和用于基因治疗的蛋白质特别有价值。设计的蛋白质最初使用恢复和置信度指标评估其保存自然结构的能力,随后使用AlphaFold工具进行评估。此外,利用遗传算法对天然蛋白序列进行突变,并与本方法设计的序列进行比较。结果表明,该方法生成的蛋白质序列与天然蛋白质序列和结构具有更大的相似性。所设计蛋白质的代码和序列可在https://github.com/aysenursoyturk/HMHO上获得。
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来源期刊
Proteins-Structure Function and Bioinformatics
Proteins-Structure Function and Bioinformatics 生物-生化与分子生物学
CiteScore
5.90
自引率
3.40%
发文量
172
审稿时长
3 months
期刊介绍: PROTEINS : Structure, Function, and Bioinformatics publishes original reports of significant experimental and analytic research in all areas of protein research: structure, function, computation, genetics, and design. The journal encourages reports that present new experimental or computational approaches for interpreting and understanding data from biophysical chemistry, structural studies of proteins and macromolecular assemblies, alterations of protein structure and function engineered through techniques of molecular biology and genetics, functional analyses under physiologic conditions, as well as the interactions of proteins with receptors, nucleic acids, or other specific ligands or substrates. Research in protein and peptide biochemistry directed toward synthesizing or characterizing molecules that simulate aspects of the activity of proteins, or that act as inhibitors of protein function, is also within the scope of PROTEINS. In addition to full-length reports, short communications (usually not more than 4 printed pages) and prediction reports are welcome. Reviews are typically by invitation; authors are encouraged to submit proposed topics for consideration.
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