IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Journal of Proteome Research Pub Date : 2025-04-04 Epub Date: 2025-02-28 DOI:10.1021/acs.jproteome.4c00877
Karl F Poncha, Alyssa T Paparella, Nicolas L Young
{"title":"Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data.","authors":"Karl F Poncha, Alyssa T Paparella, Nicolas L Young","doi":"10.1021/acs.jproteome.4c00877","DOIUrl":null,"url":null,"abstract":"<p><p>Histone proteoforms, often presenting multiple co-occurring post-translational modifications (PTMs), are central to chromatin regulation and gene expression. A proteoform is a specific form of a protein that includes variations arising from genetic changes, alternative RNA splicing, proteolytic processing, and PTMs. Genome-indexed histone proteoforms define the histone code, influencing cellular phenotype by dictating DNA interacting partners. Understanding the dynamics of histone proteoforms is essential for elucidating chromatin-based regulatory mechanisms. Advances in middle-down and top-down proteomics enable accurate identification and quantitation of thousands of proteoforms in a single run. However, the resulting data complexity presents significant challenges for analysis and visualization. Here, we introduce two new computational methods to analyze the dynamics of histone PTMs and demonstrate their use in mouse organs during aging. The score that we term \"normalized interplay\" addresses limitations of the original crosstalk score \"interplay\" providing a more complete and accurate measure of PTM crosstalk. The second score, Δ<i>I</i> or \"directional interplay\" is an asymmetric measure quantifying the magnitude and directionality of crosstalk between PTMs. Applying our two-stage scoring approach to data from CrosstalkDB reveals the dynamics of histone H3 modifications during aging.</p>","PeriodicalId":48,"journal":{"name":"Journal of Proteome Research","volume":" ","pages":"1765-1777"},"PeriodicalIF":3.8000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Proteome Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.4c00877","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

组蛋白蛋白形式通常会出现多种共存的翻译后修饰(PTM),是染色质调控和基因表达的核心。蛋白形态是蛋白质的一种特定形式,包括由基因变化、RNA 的替代剪接、蛋白水解加工和 PTMs 引起的变异。基因组索引组蛋白蛋白形式定义了组蛋白密码,通过决定DNA相互作用伙伴来影响细胞表型。了解组蛋白蛋白形式的动态对于阐明基于染色质的调控机制至关重要。中间向下和自上而下蛋白质组学的进步使得一次运行就能准确鉴定和定量数千种蛋白质形式。然而,由此产生的数据复杂性给分析和可视化带来了巨大挑战。在这里,我们介绍了两种分析组蛋白 PTM 动态的新计算方法,并展示了它们在衰老过程中小鼠器官中的应用。我们称之为 "归一化相互影响 "的分数解决了原始串扰分数 "相互影响 "的局限性,提供了一个更完整、更准确的 PTM 串扰测量方法。第二个得分ΔI 或 "定向相互作用 "是一种非对称测量方法,可量化 PTM 之间串扰的程度和方向性。将我们的两阶段评分方法应用于来自 CrosstalkDB 的数据,揭示了组蛋白 H3 修饰在衰老过程中的动态变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data.

Histone proteoforms, often presenting multiple co-occurring post-translational modifications (PTMs), are central to chromatin regulation and gene expression. A proteoform is a specific form of a protein that includes variations arising from genetic changes, alternative RNA splicing, proteolytic processing, and PTMs. Genome-indexed histone proteoforms define the histone code, influencing cellular phenotype by dictating DNA interacting partners. Understanding the dynamics of histone proteoforms is essential for elucidating chromatin-based regulatory mechanisms. Advances in middle-down and top-down proteomics enable accurate identification and quantitation of thousands of proteoforms in a single run. However, the resulting data complexity presents significant challenges for analysis and visualization. Here, we introduce two new computational methods to analyze the dynamics of histone PTMs and demonstrate their use in mouse organs during aging. The score that we term "normalized interplay" addresses limitations of the original crosstalk score "interplay" providing a more complete and accurate measure of PTM crosstalk. The second score, ΔI or "directional interplay" is an asymmetric measure quantifying the magnitude and directionality of crosstalk between PTMs. Applying our two-stage scoring approach to data from CrosstalkDB reveals the dynamics of histone H3 modifications during aging.

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:481959085
Book学术官方微信