ProPickML:在无标签靶向蛋白质组学中使用自动峰值拾取推进临床诊断。

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Journal of Proteome Research Pub Date : 2025-01-03 Epub Date: 2024-12-07 DOI:10.1021/acs.jproteome.4c00689
Elloise Coyle, Mickaël Leclercq, Clarisse Gotti, Florence Roux-Dalvai, Arnaud Droit
{"title":"ProPickML:在无标签靶向蛋白质组学中使用自动峰值拾取推进临床诊断。","authors":"Elloise Coyle, Mickaël Leclercq, Clarisse Gotti, Florence Roux-Dalvai, Arnaud Droit","doi":"10.1021/acs.jproteome.4c00689","DOIUrl":null,"url":null,"abstract":"<p><p>In targeted proteomics utilizing Selected Reaction Monitoring (SRM), the precise detection of specific peptides within complex mixtures remains a significant challenge, particularly due to noise and interference in chromatograms. Existing methodologies, such as isotopic labeling and scoring algorithms, offer partial solutions but are constrained by high run times and elevated false discovery rates. To address these limitations, we have developed ProPickML a machine learning-based tool designed to accurately identify peptide peaks across diverse data sets, independent of the assumed presence of the peptide. This model was trained on a manually labeled data set and subsequently validated to assess its predictive accuracy. The results demonstrate that the model reliably identifies peptide peaks in the presence of noise, achieving a Matthews correlation coefficient (MCC) of 0.81 on an independent test data set, surpassing mProphet's MCC of 0.71. Implemented in R as ProPickML, this tool offers a competitive, cost-effective alternative to existing techniques, significantly reducing reliance on isotopic labeling and enhancing the accuracy of peptide identification in SRM workflows.</p>","PeriodicalId":48,"journal":{"name":"Journal of Proteome Research","volume":" ","pages":"244-255"},"PeriodicalIF":3.6000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11705220/pdf/","citationCount":"0","resultStr":"{\"title\":\"ProPickML: Advancing Clinical Diagnostics with Automated Peak Picking in Label-Free Targeted Proteomics.\",\"authors\":\"Elloise Coyle, Mickaël Leclercq, Clarisse Gotti, Florence Roux-Dalvai, Arnaud Droit\",\"doi\":\"10.1021/acs.jproteome.4c00689\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In targeted proteomics utilizing Selected Reaction Monitoring (SRM), the precise detection of specific peptides within complex mixtures remains a significant challenge, particularly due to noise and interference in chromatograms. Existing methodologies, such as isotopic labeling and scoring algorithms, offer partial solutions but are constrained by high run times and elevated false discovery rates. To address these limitations, we have developed ProPickML a machine learning-based tool designed to accurately identify peptide peaks across diverse data sets, independent of the assumed presence of the peptide. This model was trained on a manually labeled data set and subsequently validated to assess its predictive accuracy. The results demonstrate that the model reliably identifies peptide peaks in the presence of noise, achieving a Matthews correlation coefficient (MCC) of 0.81 on an independent test data set, surpassing mProphet's MCC of 0.71. Implemented in R as ProPickML, this tool offers a competitive, cost-effective alternative to existing techniques, significantly reducing reliance on isotopic labeling and enhancing the accuracy of peptide identification in SRM workflows.</p>\",\"PeriodicalId\":48,\"journal\":{\"name\":\"Journal of Proteome Research\",\"volume\":\" \",\"pages\":\"244-255\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-01-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11705220/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Proteome Research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jproteome.4c00689\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Proteome Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.4c00689","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

在利用选择性反应监测(SRM)的靶向蛋白质组学中,在复杂混合物中精确检测特定肽仍然是一个重大挑战,特别是由于色谱中的噪声和干扰。现有的方法,如同位素标记和评分算法,提供了部分解决方案,但受到高运行时间和高错误发现率的限制。为了解决这些限制,我们开发了ProPickML,这是一种基于机器学习的工具,旨在准确识别不同数据集中的肽峰,而不依赖于肽的假设存在。该模型在手动标记的数据集上进行训练,并随后验证以评估其预测准确性。结果表明,该模型在存在噪声的情况下可靠地识别肽峰,在独立测试数据集上实现了0.81的马修斯相关系数(MCC),超过了mProphet的0.71的MCC。该工具以ProPickML的形式在R中实现,为现有技术提供了一种具有竞争力,具有成本效益的替代方案,显着减少了对同位素标记的依赖,并提高了SRM工作流程中肽鉴定的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ProPickML: Advancing Clinical Diagnostics with Automated Peak Picking in Label-Free Targeted Proteomics.

ProPickML: Advancing Clinical Diagnostics with Automated Peak Picking in Label-Free Targeted Proteomics.

ProPickML: Advancing Clinical Diagnostics with Automated Peak Picking in Label-Free Targeted Proteomics.

ProPickML: Advancing Clinical Diagnostics with Automated Peak Picking in Label-Free Targeted Proteomics.

In targeted proteomics utilizing Selected Reaction Monitoring (SRM), the precise detection of specific peptides within complex mixtures remains a significant challenge, particularly due to noise and interference in chromatograms. Existing methodologies, such as isotopic labeling and scoring algorithms, offer partial solutions but are constrained by high run times and elevated false discovery rates. To address these limitations, we have developed ProPickML a machine learning-based tool designed to accurately identify peptide peaks across diverse data sets, independent of the assumed presence of the peptide. This model was trained on a manually labeled data set and subsequently validated to assess its predictive accuracy. The results demonstrate that the model reliably identifies peptide peaks in the presence of noise, achieving a Matthews correlation coefficient (MCC) of 0.81 on an independent test data set, surpassing mProphet's MCC of 0.71. Implemented in R as ProPickML, this tool offers a competitive, cost-effective alternative to existing techniques, significantly reducing reliance on isotopic labeling and enhancing the accuracy of peptide identification in SRM workflows.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Proteome Research
Journal of Proteome Research 生物-生化研究方法
CiteScore
9.00
自引率
4.50%
发文量
251
审稿时长
3 months
期刊介绍: Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信