循环血液蛋白质组学的标准化框架。

IF 29 1区 生物学 Q1 GENETICS & HEREDITY
Xue Cai,Philipp E Geyer,Yasset Perez-Riverol,Gilbert S Omenn,Lianhua Dong,Robert Winkler,Sara Ahadi,Philip Lössl,Xiaobo Yu,Cheng Chang,Markus Ralser,Connie R Jimenez,Yang Zhao,Yu-Ju Chen,Terence C W Poon,Nicolai Bache,Leming Shi,Xinhua Dai,Ziyue Wang,Yi Zhu,Xiang Fang,Jochen M Schwenk,Jennifer E Van Eyk,Uwe Völker,Tiannan Guo
{"title":"循环血液蛋白质组学的标准化框架。","authors":"Xue Cai,Philipp E Geyer,Yasset Perez-Riverol,Gilbert S Omenn,Lianhua Dong,Robert Winkler,Sara Ahadi,Philip Lössl,Xiaobo Yu,Cheng Chang,Markus Ralser,Connie R Jimenez,Yang Zhao,Yu-Ju Chen,Terence C W Poon,Nicolai Bache,Leming Shi,Xinhua Dai,Ziyue Wang,Yi Zhu,Xiang Fang,Jochen M Schwenk,Jennifer E Van Eyk,Uwe Völker,Tiannan Guo","doi":"10.1038/s41588-025-02319-7","DOIUrl":null,"url":null,"abstract":"The circulating blood proteome holds immense potential for biomarker discovery and understanding disease mechanisms. Notable advances in mass spectrometry and affinity-based technologies have been made, but data integration across studies and platforms is hindered by the absence of unified analytical standards. This limitation impedes comprehensive exploration of human biology across diverse phenotypes and cohorts as well as the translation of findings into clinical applications. The disparities between datasets, stemming from a combination of factors related to differences in sample collection, pre-analytical handling, measurement methods and instrumentation, further complicate data integration. In this Perspective, we outline key challenges in blood-based proteomics and propose actionable strategies. Central to our recommendations are high-quality, technology-agnostic reference samples, which can bridge disparate datasets and enable robust cross-study comparisons. By fostering interconnected investigations across proteomic technologies, blood sample collections, clinical phenotypes and different populations, these references will accelerate the field and its translation.","PeriodicalId":18985,"journal":{"name":"Nature genetics","volume":"3 1","pages":""},"PeriodicalIF":29.0000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A standardized framework for circulating blood proteomics.\",\"authors\":\"Xue Cai,Philipp E Geyer,Yasset Perez-Riverol,Gilbert S Omenn,Lianhua Dong,Robert Winkler,Sara Ahadi,Philip Lössl,Xiaobo Yu,Cheng Chang,Markus Ralser,Connie R Jimenez,Yang Zhao,Yu-Ju Chen,Terence C W Poon,Nicolai Bache,Leming Shi,Xinhua Dai,Ziyue Wang,Yi Zhu,Xiang Fang,Jochen M Schwenk,Jennifer E Van Eyk,Uwe Völker,Tiannan Guo\",\"doi\":\"10.1038/s41588-025-02319-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The circulating blood proteome holds immense potential for biomarker discovery and understanding disease mechanisms. Notable advances in mass spectrometry and affinity-based technologies have been made, but data integration across studies and platforms is hindered by the absence of unified analytical standards. This limitation impedes comprehensive exploration of human biology across diverse phenotypes and cohorts as well as the translation of findings into clinical applications. The disparities between datasets, stemming from a combination of factors related to differences in sample collection, pre-analytical handling, measurement methods and instrumentation, further complicate data integration. In this Perspective, we outline key challenges in blood-based proteomics and propose actionable strategies. Central to our recommendations are high-quality, technology-agnostic reference samples, which can bridge disparate datasets and enable robust cross-study comparisons. By fostering interconnected investigations across proteomic technologies, blood sample collections, clinical phenotypes and different populations, these references will accelerate the field and its translation.\",\"PeriodicalId\":18985,\"journal\":{\"name\":\"Nature genetics\",\"volume\":\"3 1\",\"pages\":\"\"},\"PeriodicalIF\":29.0000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature genetics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41588-025-02319-7\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41588-025-02319-7","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

循环血液蛋白质组在发现生物标志物和理解疾病机制方面具有巨大的潜力。质谱和基于亲和力的技术取得了显著进展,但由于缺乏统一的分析标准,阻碍了跨研究和平台的数据集成。这一限制阻碍了对不同表型和群体的人类生物学的全面探索,以及将研究结果转化为临床应用。数据集之间的差异,源于与样本收集、分析前处理、测量方法和仪器的差异相关的综合因素,进一步使数据集成复杂化。从这个角度来看,我们概述了基于血液的蛋白质组学的主要挑战,并提出了可行的策略。我们建议的核心是高质量的、与技术无关的参考样本,它可以连接不同的数据集,并实现可靠的交叉研究比较。通过促进跨蛋白质组学技术、血液样本收集、临床表型和不同人群的相互关联的调查,这些参考文献将加速该领域及其转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A standardized framework for circulating blood proteomics.
The circulating blood proteome holds immense potential for biomarker discovery and understanding disease mechanisms. Notable advances in mass spectrometry and affinity-based technologies have been made, but data integration across studies and platforms is hindered by the absence of unified analytical standards. This limitation impedes comprehensive exploration of human biology across diverse phenotypes and cohorts as well as the translation of findings into clinical applications. The disparities between datasets, stemming from a combination of factors related to differences in sample collection, pre-analytical handling, measurement methods and instrumentation, further complicate data integration. In this Perspective, we outline key challenges in blood-based proteomics and propose actionable strategies. Central to our recommendations are high-quality, technology-agnostic reference samples, which can bridge disparate datasets and enable robust cross-study comparisons. By fostering interconnected investigations across proteomic technologies, blood sample collections, clinical phenotypes and different populations, these references will accelerate the field and its translation.
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
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
×
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