通过机器学习预测抗体-抗原结合:数据集的开发和方法的评估
Chao Ye1, Wenxing Hu2, Bruno Gaeta1
1School of Computer Science and Engineering, The University of New South Wales, Sydney, Australia.
JMIR bioinformatics and biotechnology
|June 27, 2024
概括
机器学习从序列数据准确地预测了抗体与抗原的结合. 用BLOSUM62的近邻方法实现了82%的准确性,为免疫学研究提供了有价值的工具.
科学领域:
- 免疫学 免疫学 免疫学
- 生物信息学是一种生物信息学.
- 计算生物学 计算生物学
背景情况:
- 哺乳动物的免疫系统产生对各种抗原的抗体.
- 从DNA测序中预测抗体-抗原相互作用对于理解免疫反应至关重要.
- 目前的方法缺乏高通量,基于序列的抗体识别预测.
研究的目的:
- 用序列数据比较机器学习 (ML) 方法来预测使用序列数据的抗体-抗原结合.
- 开发一种仅从序列信息预测抗体-抗原相互作用的方法.
主要方法:
- 从蛋白质数据库和冠状病毒抗体数据库编译了抗体-抗原对数据.
- 使用分子对接生成了额外的数据.
- 应用并比较了ML方法:加权的最近邻居,与BLOSUM62的最近邻居和随机森林.
主要成果:
- 该数据集包括1157个抗体,57个抗原和5041对.
- 使用BLOSUM62的近邻方法实现了最高的预测准确率,约为82%.
- 在抗体-抗原结合预测中建立了ML和数据集创建的基准.
结论:
- 机器学习有效地从蛋白质序列中预测抗体-抗原相互作用.
- 开发的数据集和Python程序在GitHub上公开提供.
- 这项工作为预测免疫学的未来研究提供了框架和资源.
相关概念视频
Antibody Actions
1.1K
Antibodies, or immunoglobulins, are critical players in the immune system's arsenal against invading pathogens. Produced by B cells and plasma cells, their primary role is to detect and bind to specific antigens, molecules found on the surface of pathogens like bacteria or viruses. Beyond antigen recognition, antibodies perform several vital functions that contribute to immune defense.
Neutralization
Antibodies can bind to pathogens, preventing them from infecting host cells. This process...
Neutralization
Antibodies can bind to pathogens, preventing them from infecting host cells. This process...
1.1K
Antibody Structure
59.9K
Overview
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
Antibodies consist of four polypeptide chains: two identical heavy...
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
Antibodies consist of four polypeptide chains: two identical heavy...
59.9K
Conserved Binding Sites
4.2K
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
4.2K
Affinity and Avidity
35.9K
Overview
35.9K
Ligand Binding Sites
12.8K
Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
12.8K
Protein-protein Interfaces
12.5K
Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
12.5K


