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CLAPE:通过蛋白质语言模型进行蛋白质-配体结合位点预测。

CLAPE: Protein-Ligand Binding Site Prediction via Protein Language Models.

作者信息

Liu Yufan, Tian Boxue

机构信息

Computer Science Program, Computer, Electrical and Mathematical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.

MOE Key Laboratory of Bioinformatics, State Key Laboratory of Molecular Oncology, School of Pharmaceutical Sciences, Tsinghua University, Beijing, China.

出版信息

Methods Mol Biol. 2025;2941:293-311. doi: 10.1007/978-1-0716-4623-6_18.

Abstract

Protein-ligand interactions are fundamental to critical biological processes such as transcription, translation, and drug-target interaction. The precise identification of protein-ligand binding residues is essential for accurately modeling these interactions and facilitating subsequent research. However, the development of computational methods that are both efficient and accurate for this purpose remains a significant challenge. Progress in this field holds the potential to drive substantial advancements in biotechnology and drug discovery. In response to this need, we have recently developed a method known as Contrastive Learning And Pretrained Encoder (CLAPE). This approach integrates a pretrained protein language model with contrastive learning to predict ligand-binding residues. In this chapter, we provided a detailed overview of the CLAPE framework, including instructions for using the associated Python package and command-line tools. Additionally, we outline the methods employed for result visualization and describe the comprehensive processes involved in model training.

摘要

蛋白质-配体相互作用对于转录、翻译和药物-靶点相互作用等关键生物学过程至关重要。精确识别蛋白质-配体结合残基对于准确模拟这些相互作用并促进后续研究至关重要。然而,为此目的开发高效且准确的计算方法仍然是一项重大挑战。该领域的进展有可能推动生物技术和药物发现的重大进步。为了满足这一需求,我们最近开发了一种称为对比学习与预训练编码器(CLAPE)的方法。这种方法将预训练的蛋白质语言模型与对比学习相结合,以预测配体结合残基。在本章中,我们详细概述了CLAPE框架,包括使用相关Python包和命令行工具的说明。此外,我们概述了用于结果可视化的方法,并描述了模型训练所涉及的全面过程。

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