一个基于特征组合和智能搜索的蛋白质健康预测框架
Zhihui Zhang1, Zhixuan Li1, Qianyue Wang2
1Guangdong Key Laboratory of Fermentation and Enzyme Engineering, School of Biology and Biological Engineering, South China University of Technology, Guangzhou, China.
Protein science : a publication of the Protein Society
|November 15, 2024
概括
我们开发了scut_ProFP,这是一个用于蛋白质工程的机器学习 (ML) 框架. 它通过结合和选择序列特征,有效地预测蛋白质适应性,优于现有方法,并允许准确的序列到功能映射.
科学领域:
- 生物技术是生物技术.
- 计算生物学 计算生物学
- 蛋白质工程是指蛋白质工程.
背景情况:
- 机器学习 (ML) 模型从序列中预测蛋白质功能,但需要从有限的数据中有效地提取特征.
- 优化ML性能取决于识别蛋白质序列中的相关功能特征.
研究的目的:
- 开发一个新的预测框架, scut_ProFP,用于增强蛋白质工程.
- 通过使用集成特征工程技术,提高序列到功能映射的准确性.
主要方法:
- scut_ProFP集成了功能组合,用于全面的序列表示和功能选择,以识别最佳功能.
- 该框架与已建立的ML模型 (如ECNet,EVmutation和UniRep) 相比进行了基准测试.
- scut_ProFP 证明了从低阶突变体到高阶突变体的概括能力.
主要成果:
- scut_ProFP与现有框架相比,实现了更高的性能,并与复杂的深度学习模型竞争.
- 该方法成功模拟了CreiLOV光蛋白的工程,从有限的低光数据中丰富了高光突变物.
- scut_ProFP 能够对突变序列进行准确的序列到功能预测和跨突变序列的概括.
结论:
- scut_ProFP为蛋白质工程中的机器学习提供了一种有效的,数据驱动的方法.
- 该框架增强了蛋白质适应性的预测,并促进了具有所需功能的蛋白质的发现.
- 开发的方法为加速蛋白质设计和工程工作提供了有价值的工具.
相关概念视频
Inclusive Fitness
35.9K
Most altruistic behavior—in which one animal helps another at a cost to themselves—occurs between relatives. Scientists think these altruistic behaviors evolved because they increase the inclusive fitness of the animal providing help.
35.9K
Protein Networks
3.9K
An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
3.9K
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
Sensitivity, Specificity, and Predicted Value
194
In healthcare diagnostics, laboratory tests play a crucial role in identifying and diagnosing a wide range of medical conditions. However, interpreting test results is not always straightforward. An abnormal test result does not always confirm the presence of a disease, just as a normal result does not guarantee its absence. To assess the reliability of these diagnostic tools, healthcare practitioners rely on two key statistical indicators: sensitivity and specificity.
Sensitivity is the...
Sensitivity is the...
194
Protein Families
15.3K
Protein families are groups of homologous proteins; that is, they have similarities in amino acid sequences and three-dimensional structures. Protein families usually occur because of gene duplication, where an additional copy of a gene is inserted into the genome of an organism. Mutations that change the amino acids but still allow the protein to be properly synthesized, will lead to new protein family members. If these new proteins contain similar amino acids in key...
15.3K
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


