ActivePPI: quantifying protein-protein interaction network activity with Markov random fields.

IF 4.4 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Bioinformatics Pub Date : 2023-09-02 DOI:10.1093/bioinformatics/btad567
Chuanyuan Wang, Shiyu Xu, Duanchen Sun, Zhi-Ping Liu
{"title":"ActivePPI: quantifying protein-protein interaction network activity with Markov random fields.","authors":"Chuanyuan Wang,&nbsp;Shiyu Xu,&nbsp;Duanchen Sun,&nbsp;Zhi-Ping Liu","doi":"10.1093/bioinformatics/btad567","DOIUrl":null,"url":null,"abstract":"<p><strong>Motivation: </strong>Protein-protein interactions (PPI) are crucial components of the biomolecular networks that enable cells to function. Biological experiments have identified a large number of PPI, and these interactions are stored in knowledge bases. However, these interactions are often restricted to specific cellular environments and conditions. Network activity can be characterized as the extent of agreement between a PPI network (PPIN) and a distinct cellular environment measured by protein mass spectrometry, and it can also be quantified as a statistical significance score. Without knowing the activity of these PPI in the cellular environments or specific phenotypes, it is impossible to reveal how these PPI perform and affect cellular functioning.</p><p><strong>Results: </strong>To calculate the activity of PPIN in different cellular conditions, we proposed a PPIN activity evaluation framework named ActivePPI to measure the consistency between network architecture and protein measurement data. ActivePPI estimates the probability density of protein mass spectrometry abundance and models PPIN using a Markov-random-field-based method. Furthermore, empirical P-value is derived based on a nonparametric permutation test to quantify the likelihood significance of the match between PPIN structure and protein abundance data. Extensive numerical experiments demonstrate the superior performance of ActivePPI and result in network activity evaluation, pathway activity assessment, and optimal network architecture tuning tasks. To summarize it succinctly, ActivePPI is a versatile tool for evaluating PPI network that can uncover the functional significance of protein interactions in crucial cellular biological processes and offer further insights into physiological phenomena.</p><p><strong>Availability and implementation: </strong>All source code and data are freely available at https://github.com/zpliulab/ActivePPI.</p>","PeriodicalId":8903,"journal":{"name":"Bioinformatics","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2023-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516639/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bioinformatics/btad567","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Motivation: Protein-protein interactions (PPI) are crucial components of the biomolecular networks that enable cells to function. Biological experiments have identified a large number of PPI, and these interactions are stored in knowledge bases. However, these interactions are often restricted to specific cellular environments and conditions. Network activity can be characterized as the extent of agreement between a PPI network (PPIN) and a distinct cellular environment measured by protein mass spectrometry, and it can also be quantified as a statistical significance score. Without knowing the activity of these PPI in the cellular environments or specific phenotypes, it is impossible to reveal how these PPI perform and affect cellular functioning.

Results: To calculate the activity of PPIN in different cellular conditions, we proposed a PPIN activity evaluation framework named ActivePPI to measure the consistency between network architecture and protein measurement data. ActivePPI estimates the probability density of protein mass spectrometry abundance and models PPIN using a Markov-random-field-based method. Furthermore, empirical P-value is derived based on a nonparametric permutation test to quantify the likelihood significance of the match between PPIN structure and protein abundance data. Extensive numerical experiments demonstrate the superior performance of ActivePPI and result in network activity evaluation, pathway activity assessment, and optimal network architecture tuning tasks. To summarize it succinctly, ActivePPI is a versatile tool for evaluating PPI network that can uncover the functional significance of protein interactions in crucial cellular biological processes and offer further insights into physiological phenomena.

Availability and implementation: All source code and data are freely available at https://github.com/zpliulab/ActivePPI.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ActivePPI:用马尔可夫随机场量化蛋白质-蛋白质相互作用网络活性。
动机:蛋白质-蛋白质相互作用(PPI)是使细胞发挥功能的生物分子网络的关键组成部分。生物实验已经确定了大量的PPI,并且这些相互作用存储在知识库中。然而,这些相互作用通常局限于特定的细胞环境和条件。网络活性可以表征为PPI网络(PPIN)与蛋白质质谱法测量的不同细胞环境之间的一致程度,也可以量化为统计显著性得分。如果不知道这些PPI在细胞环境或特定表型中的活性,就不可能揭示这些PPI是如何表现和影响细胞功能的。结果:为了计算PPIN在不同细胞条件下的活性,我们提出了一个名为ActivePPI的PPIN活性评估框架,以测量网络结构和蛋白质测量数据之间的一致性。ActivePPI估计蛋白质质谱丰度的概率密度,并使用基于马尔可夫随机场的方法对PPIN进行建模。此外,基于非参数排列检验推导了经验P值,以量化PPIN结构和蛋白质丰度数据之间匹配的似然显著性。大量的数值实验证明了ActivePPI的优越性能,并导致了网络活动评估、路径活动评估和最佳网络架构调整任务。简而言之,ActivePPI是一种评估PPI网络的通用工具,可以揭示蛋白质相互作用在关键细胞生物学过程中的功能意义,并对生理现象提供进一步的见解。可用性和实现:所有源代码和数据均可在https://github.com/zpliulab/ActivePPI.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Bioinformatics
Bioinformatics 生物-生化研究方法
CiteScore
11.20
自引率
5.20%
发文量
753
审稿时长
2.1 months
期刊介绍: The leading journal in its field, Bioinformatics publishes the highest quality scientific papers and review articles of interest to academic and industrial researchers. Its main focus is on new developments in genome bioinformatics and computational biology. Two distinct sections within the journal - Discovery Notes and Application Notes- focus on shorter papers; the former reporting biologically interesting discoveries using computational methods, the latter exploring the applications used for experiments.
期刊最新文献
PQSDC: a parallel lossless compressor for quality scores data via sequences partition and Run-Length prediction mapping. MUSE-XAE: MUtational Signature Extraction with eXplainable AutoEncoder enhances tumour types classification. CopyVAE: a variational autoencoder-based approach for copy number variation inference using single-cell transcriptomics CORDAX web server: An online platform for the prediction and 3D visualization of aggregation motifs in protein sequences. LMCrot: An enhanced protein crotonylation site predictor by leveraging an interpretable window-level embedding from a transformer-based protein language model.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1