AlphaCross-XL: A Seamless Tool for Automated and Proteome-Scale Mapping of Cross-Linked Peptides Onto 3D Protein Structures.

IF 5.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Sanjyot Vinayak Shenoy, Deeptarup Biswas, Arthur Zalevsky, Audrey Kishishita, Ayushi Verma, Ishan Upadhay, Yi He, Andrej Sali, Rosa Viner, Kamal Mandal, Sanjeeva Srivastava, Arun P Wiita
{"title":"AlphaCross-XL: A Seamless Tool for Automated and Proteome-Scale Mapping of Cross-Linked Peptides Onto 3D Protein Structures.","authors":"Sanjyot Vinayak Shenoy, Deeptarup Biswas, Arthur Zalevsky, Audrey Kishishita, Ayushi Verma, Ishan Upadhay, Yi He, Andrej Sali, Rosa Viner, Kamal Mandal, Sanjeeva Srivastava, Arun P Wiita","doi":"10.1016/j.mcpro.2025.101057","DOIUrl":null,"url":null,"abstract":"<p><p>Crosslinking mass spectrometry (XL-MS) is an exciting proteomics technology to capture native protein conformations in real time within biological systems. Historically, however, implementation of this technology has typically been limited to single purified recombinant proteins or in vitro-assembled protein complexes. These limitations are associated with inherent challenges in XL-MS analysis, including extremely low abundance of crosslinked (XL) peptides and complex deconvolution of XL peptide-derived spectral data. However, impressive recent developments in computation and instrumentation have now made it feasible to address biological questions using proteome-wide XL-MS analysis. Although some XL mapping software tools exist, these require manual input of specific Protein Data Bank structures at the single protein level and do not function at the high-throughput scale required to analyze datasets derived from thousands of proteins. To address this need, we therefore sought to develop a strategy enabling automated mapping of XL peptides onto the 3D structures of proteins, at a proteome-wide scale. Herein, we describe AlphaCross-XL, a first-in-class seamless computational tool for automated mapping of XL peptides onto the protein structures for intraprotein crosslinks and loop links. The AlphaCross-XL software first retrieves protein structures from the AlphaFold Protein Structure Database and maps all the identified crosslinks onto the 3D structure. It also calculates the Euclidian distance between the crosslinked residues and reports the violated and satisfied crosslink distances based on a user-defined distance threshold, which is visually discriminated by color in PyMOL. Last, the tool also supports further validation of user-submitted protein structures, which can include any computer-predicted protein structure and experimentally derived protein structures (i.e., from Protein Data Bank). AlphaCross-XL is available at https://github.com/sanjyotshenoy/alphacross-xl.</p>","PeriodicalId":18712,"journal":{"name":"Molecular & Cellular Proteomics","volume":" ","pages":"101057"},"PeriodicalIF":5.5000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular & Cellular Proteomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mcpro.2025.101057","RegionNum":2,"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

Crosslinking mass spectrometry (XL-MS) is an exciting proteomics technology to capture native protein conformations in real time within biological systems. Historically, however, implementation of this technology has typically been limited to single purified recombinant proteins or in vitro-assembled protein complexes. These limitations are associated with inherent challenges in XL-MS analysis, including extremely low abundance of crosslinked (XL) peptides and complex deconvolution of XL peptide-derived spectral data. However, impressive recent developments in computation and instrumentation have now made it feasible to address biological questions using proteome-wide XL-MS analysis. Although some XL mapping software tools exist, these require manual input of specific Protein Data Bank structures at the single protein level and do not function at the high-throughput scale required to analyze datasets derived from thousands of proteins. To address this need, we therefore sought to develop a strategy enabling automated mapping of XL peptides onto the 3D structures of proteins, at a proteome-wide scale. Herein, we describe AlphaCross-XL, a first-in-class seamless computational tool for automated mapping of XL peptides onto the protein structures for intraprotein crosslinks and loop links. The AlphaCross-XL software first retrieves protein structures from the AlphaFold Protein Structure Database and maps all the identified crosslinks onto the 3D structure. It also calculates the Euclidian distance between the crosslinked residues and reports the violated and satisfied crosslink distances based on a user-defined distance threshold, which is visually discriminated by color in PyMOL. Last, the tool also supports further validation of user-submitted protein structures, which can include any computer-predicted protein structure and experimentally derived protein structures (i.e., from Protein Data Bank). AlphaCross-XL is available at https://github.com/sanjyotshenoy/alphacross-xl.

AlphaCross-XL:一个无缝的工具,用于自动和蛋白质组尺度的交联肽映射到三维蛋白质结构。
交联质谱(XL-MS)是一种令人兴奋的蛋白质组学技术,可以实时捕获生物系统中的天然蛋白质构象。然而,从历史上看,该技术的实施通常仅限于单一纯化的重组蛋白或体外组装的蛋白复合物。这些限制与XL- ms分析固有的挑战有关,包括极低丰度的交联(XL)肽和XL肽衍生的光谱数据的复杂反褶积。然而,最近在计算和仪器方面令人印象深刻的发展,现在使得使用蛋白质组范围的xml - ms分析来解决生物学问题成为可能。虽然存在一些XL绘图软件工具,但这些工具需要在单个蛋白质水平上手动输入特定的蛋白质数据库(PDB)结构,并且无法在分析来自数千种蛋白质的数据集所需的高通量规模上发挥作用。为了满足这一需求,我们因此寻求开发一种策略,能够在蛋白质组范围内将XL肽自动映射到蛋白质的三维(3D)结构上。在这里,我们描述了AlphaCross-XL,一个一流的无缝计算工具,用于自动将XL肽映射到蛋白质结构上,用于蛋白质内交联和环连接。AlphaCross-XL软件首先从AlphaFold蛋白质结构数据库中检索蛋白质结构,并将所有已识别的交联映射到3D结构上。它还计算交联残基之间的欧几里德距离,并根据用户定义的距离阈值报告违反和满足的交联距离,在PyMOL中可以通过颜色直观地区分。最后,该工具还支持进一步验证用户提交的蛋白质结构,可以包括任何计算机预测的蛋白质结构和实验衍生的蛋白质结构(即来自PDB)。AlphaCross-XL可在https://github.com/sanjyotshenoy/alphacross-xl上获得。
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 求助全文
来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
×
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