• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 IS-PRM 的肽靶向策略,结合长读测序,用于发现替代蛋白质组。

IS-PRM-Based Peptide Targeting Informed by Long-Read Sequencing for Alternative Proteome Detection.

机构信息

Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, Virginia 22903, United States.

Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia 22903, United States.

出版信息

J Am Soc Mass Spectrom. 2024 Nov 6;35(11):2614-2630. doi: 10.1021/jasms.4c00119. Epub 2024 Jul 16.

DOI:10.1021/jasms.4c00119
PMID:39012054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11544703/
Abstract

Alternative splicing is a major contributor of transcriptomic complexity, but the extent to which transcript isoforms are translated into stable, functional protein isoforms is unclear. Furthermore, detection of relatively scarce isoform-specific peptides is challenging, with many protein isoforms remaining uncharted due to technical limitations. Recently, a family of advanced targeted MS strategies, termed internal standard parallel reaction monitoring (IS-PRM), have demonstrated multiplexed, sensitive detection of predefined peptides of interest. Such approaches have not yet been used to confirm existence of novel peptides. Here, we present a targeted proteogenomic approach that leverages sample-matched long-read RNA sequencing (lrRNA-seq) data to predict potential protein isoforms with prior transcript evidence. Predicted tryptic isoform-specific peptides, which are specific to individual gene product isoforms, serve as "triggers" and "targets" in the IS-PRM method, Tomahto. Using the model human stem cell line WTC11, LR RNaseq data were generated and used to inform the generation of synthetic standards for 192 isoform-specific peptides (114 isoforms from 55 genes). These synthetic "trigger" peptides were labeled with super heavy tandem mass tags (TMT) and spiked into TMT-labeled WTC11 tryptic digest, predicted to contain corresponding endogenous "target" peptides. Compared to DDA mode, Tomahto increased detectability of isoforms by 3.6-fold, resulting in the identification of five previously unannotated isoforms. Our method detected protein isoform expression for 43 out of 55 genes corresponding to 54 resolved isoforms. This lrRNA-seq-informed Tomahto targeted approach is a new modality for generating protein-level evidence of alternative isoforms─a critical first step in designing functional studies and eventually clinical assays.

摘要

可变剪接是转录组复杂性的主要贡献者,但转录本异构体转化为稳定、有功能的蛋白质异构体的程度尚不清楚。此外,由于技术限制,相对稀缺的同工型特异性肽的检测具有挑战性,许多蛋白质同工型仍然未被发现。最近,一类先进的靶向 MS 策略,称为内标平行反应监测(IS-PRM),已经证明了对感兴趣的预定义肽的多重、敏感检测。这些方法尚未用于确认新肽的存在。在这里,我们提出了一种靶向蛋白质基因组学方法,该方法利用样本匹配的长读 RNA 测序(lrRNA-seq)数据来预测具有先前转录证据的潜在蛋白质同工型。预测的胰蛋白酶同工型特异性肽,这些肽特异性地针对单个基因产物同工型,作为 IS-PRM 方法 Tomahto 的“触发器”和“靶标”。使用模型人类干细胞系 WTC11,生成了 LR RNaseq 数据,并用于生成 192 个同工型特异性肽(来自 55 个基因的 114 个同工型)的合成标准品。这些合成的“触发”肽用超重串联质量标签(TMT)标记,并掺入到 TMT 标记的 WTC11 胰蛋白酶消化物中,预测其中含有相应的内源性“靶”肽。与 DDA 模式相比,Tomahto 将同工型的可检测性提高了 3.6 倍,从而鉴定了五个以前未注释的同工型。我们的方法检测到 55 个基因中的 43 个基因对应 54 个解析同工型的蛋白质同工型表达。这种基于 lrRNA-seq 的 Tomahto 靶向方法是生成替代同工型蛋白质水平证据的新方法——这是设计功能研究并最终临床检测的关键第一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/b8330f439d2d/js4c00119_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/21184d23ce32/js4c00119_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/e37c776a8c05/js4c00119_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/a7eb99547bc7/js4c00119_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/b8330f439d2d/js4c00119_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/21184d23ce32/js4c00119_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/e37c776a8c05/js4c00119_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/a7eb99547bc7/js4c00119_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14db/11544703/b8330f439d2d/js4c00119_0004.jpg

相似文献

1
IS-PRM-Based Peptide Targeting Informed by Long-Read Sequencing for Alternative Proteome Detection.基于 IS-PRM 的肽靶向策略,结合长读测序,用于发现替代蛋白质组。
J Am Soc Mass Spectrom. 2024 Nov 6;35(11):2614-2630. doi: 10.1021/jasms.4c00119. Epub 2024 Jul 16.
2
IS-PRM-based peptide targeting informed by long-read sequencing for alternative proteome detection.基于长读长测序的IS-PRM肽靶向技术用于替代蛋白质组检测。
bioRxiv. 2024 Apr 1:2024.04.01.587549. doi: 10.1101/2024.04.01.587549.
3
Computation-assisted targeted proteomics of alternative splicing protein isoforms in the human heart.计算辅助的人类心脏中可变剪接蛋白异构体的靶向蛋白质组学分析。
J Mol Cell Cardiol. 2021 May;154:92-96. doi: 10.1016/j.yjmcc.2021.01.007. Epub 2021 Feb 5.
4
Identification of Protein Isoforms Using Reference Databases Built from Long and Short Read RNA-Sequencing.使用基于长读和短读 RNA 测序构建的参考数据库鉴定蛋白质同工型。
J Proteome Res. 2022 Jul 1;21(7):1628-1639. doi: 10.1021/acs.jproteome.1c00968. Epub 2022 May 25.
5
Long-read proteogenomics to connect disease-associated sQTLs to the protein isoform effectors of disease.长读蛋白质组学将疾病相关的 sQTL 与疾病的蛋白质同工型效应物联系起来。
Am J Hum Genet. 2024 Sep 5;111(9):1914-1931. doi: 10.1016/j.ajhg.2024.07.003. Epub 2024 Jul 29.
6
Identification of novel alternative splicing biomarkers for breast cancer with LC/MS/MS and RNA-Seq.利用 LC/MS/MS 和 RNA-Seq 鉴定乳腺癌新型可变剪接生物标志物。
BMC Bioinformatics. 2020 Dec 3;21(Suppl 9):541. doi: 10.1186/s12859-020-03824-8.
7
ASV-ID, a Proteogenomic Workflow To Predict Candidate Protein Isoforms on the Basis of Transcript Evidence.ASV-ID,一种基于转录证据预测候选蛋白异构体的蛋白质组学工作流程。
J Proteome Res. 2018 Dec 7;17(12):4235-4242. doi: 10.1021/acs.jproteome.8b00548. Epub 2018 Oct 15.
8
Identification of Differentially Expressed Splice Variants by the Proteogenomic Pipeline Splicify.通过 Proteogenomic 管道 Splicify 鉴定差异表达的剪接变体。
Mol Cell Proteomics. 2017 Oct;16(10):1850-1863. doi: 10.1074/mcp.TIR117.000056. Epub 2017 Jul 26.
9
Enhanced protein isoform characterization through long-read proteogenomics.通过长读蛋白质基因组学增强蛋白质亚型特征分析。
Genome Biol. 2022 Mar 3;23(1):69. doi: 10.1186/s13059-022-02624-y.
10
Characterization of protein isoform diversity in human umbilical vein endothelial cells via long-read proteogenomics.通过长读蛋白质基因组学对人脐静脉内皮细胞中的蛋白质同工型多样性进行表征。
RNA Biol. 2022 Jan;19(1):1228-1243. doi: 10.1080/15476286.2022.2141938.

引用本文的文献

1
Protein Sequencing with Single Amino Acid Resolution Discerns Peptides That Discriminate Tropomyosin Proteoforms.具有单氨基酸分辨率的蛋白质测序可识别区分原肌球蛋白蛋白变体的肽段。
J Proteome Res. 2025 Jun 10. doi: 10.1021/acs.jproteome.4c00978.
2
Long-read RNA sequencing: A transformative technology for exploring transcriptome complexity in human diseases.长读长RNA测序:一种探索人类疾病转录组复杂性的变革性技术。
Mol Ther. 2025 Mar 5;33(3):883-894. doi: 10.1016/j.ymthe.2024.11.025. Epub 2024 Nov 19.
3
Enhanced Sample Multiplexing-Based Targeted Proteomics with Intelligent Data Acquisition.

本文引用的文献

1
Long-read proteogenomics to connect disease-associated sQTLs to the protein isoform effectors of disease.长读蛋白质组学将疾病相关的 sQTL 与疾病的蛋白质同工型效应物联系起来。
Am J Hum Genet. 2024 Sep 5;111(9):1914-1931. doi: 10.1016/j.ajhg.2024.07.003. Epub 2024 Jul 29.
2
SQANTI3: curation of long-read transcriptomes for accurate identification of known and novel isoforms.SQANTI3:长读转录组的编目,用于准确识别已知和新的异构体。
Nat Methods. 2024 May;21(5):793-797. doi: 10.1038/s41592-024-02229-2. Epub 2024 Mar 20.
3
Accurate de novo peptide sequencing using fully convolutional neural networks.
基于增强样本多重化的靶向蛋白质组学与智能数据采集技术
J Am Soc Mass Spectrom. 2024 Oct 2;35(10):2420-2428. doi: 10.1021/jasms.4c00234. Epub 2024 Sep 10.
利用全卷积神经网络进行精确从头肽测序。
Nat Commun. 2023 Dec 2;14(1):7974. doi: 10.1038/s41467-023-43010-x.
4
Integrative Proteogenomics for Differential Expression and Splicing Variation in a DM1 Mouse Model.整合蛋白质基因组学研究DM1小鼠模型中的差异表达和剪接变异
Mol Cell Proteomics. 2024 Jan;23(1):100683. doi: 10.1016/j.mcpro.2023.100683. Epub 2023 Nov 21.
5
The UCSC Genome Browser database: 2024 update.UCSC 基因组浏览器数据库:2024 年更新。
Nucleic Acids Res. 2024 Jan 5;52(D1):D1082-D1088. doi: 10.1093/nar/gkad987.
6
Pan-cancer proteogenomics connects oncogenic drivers to functional states.泛癌蛋白质基因组学将致癌驱动因素与功能状态联系起来。
Cell. 2023 Aug 31;186(18):3921-3944.e25. doi: 10.1016/j.cell.2023.07.014. Epub 2023 Aug 14.
7
Identification of Splice Variants and Isoforms in Transcriptomics and Proteomics.转录组学和蛋白质组学中的剪接变体和同工型鉴定。
Annu Rev Biomed Data Sci. 2023 Aug 10;6:357-376. doi: 10.1146/annurev-biodatasci-020722-044021.
8
Isoform-specific functions of Ras in T-cell development and differentiation. Ras 在 T 细胞发育和分化中的同种型特异性功能。
Eur J Immunol. 2023 Jul;53(7):e2350430. doi: 10.1002/eji.202350430. Epub 2023 May 28.
9
Transformation of alignment files improves performance of variant callers for long-read RNA sequencing data.对齐文件的转换可提高长读 RNA 测序数据变异调用器的性能。
Genome Biol. 2023 Apr 24;24(1):91. doi: 10.1186/s13059-023-02923-y.
10
PepQuery2 democratizes public MS proteomics data for rapid peptide searching. PepQuery2 使公共 MS 蛋白质组学数据民主化,便于快速进行肽搜索。
Nat Commun. 2023 Apr 18;14(1):2213. doi: 10.1038/s41467-023-37462-4.