DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.

Junjie Hou, Jifeng Wang, Fuquan Yang, Tao Xu
{"title":"DIA-MS2pep: a library-free framework for comprehensive peptide identification from data-independent acquisition data.","authors":"Junjie Hou,&nbsp;Jifeng Wang,&nbsp;Fuquan Yang,&nbsp;Tao Xu","doi":"10.52601/bpr.2022.220011","DOIUrl":null,"url":null,"abstract":"<p><p>Identifying peptides directly from data-independent acquisition (DIA) data remains challenging due to the highly multiplexed MS/MS spectra. Spectral library-based peptide detection is sensitive, but it is limited to the depth of the library and mutes the discovery potential of DIA data. We present here, DIA-MS2pep, a library-free framework for comprehensive peptide identification from DIA data. DIA-MS2pep uses a data-driven algorithm for MS/MS spectrum demultiplexing using the fragments data without the need of a precursor. With a large precursor mass tolerance database search, DIA-MS2pep can identify the peptides and their modified forms. We demonstrate the performance of DIA-MS2pep by comparing it to conventional library-free tools in accuracy and sensitivity of peptide identifications using publicly available DIA datasets of varying samples, including HeLa cell lysates, phosphopeptides, plasma, <i>etc</i>. Compared with data-dependent acquisition-based spectral libraries, spectral libraries built directly from DIA data with DIA-MS2pep improve the accuracy and reproducibility of the quantitative proteome.</p>","PeriodicalId":59621,"journal":{"name":"生物物理学报:英文版","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166510/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"生物物理学报:英文版","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52601/bpr.2022.220011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Identifying peptides directly from data-independent acquisition (DIA) data remains challenging due to the highly multiplexed MS/MS spectra. Spectral library-based peptide detection is sensitive, but it is limited to the depth of the library and mutes the discovery potential of DIA data. We present here, DIA-MS2pep, a library-free framework for comprehensive peptide identification from DIA data. DIA-MS2pep uses a data-driven algorithm for MS/MS spectrum demultiplexing using the fragments data without the need of a precursor. With a large precursor mass tolerance database search, DIA-MS2pep can identify the peptides and their modified forms. We demonstrate the performance of DIA-MS2pep by comparing it to conventional library-free tools in accuracy and sensitivity of peptide identifications using publicly available DIA datasets of varying samples, including HeLa cell lysates, phosphopeptides, plasma, etc. Compared with data-dependent acquisition-based spectral libraries, spectral libraries built directly from DIA data with DIA-MS2pep improve the accuracy and reproducibility of the quantitative proteome.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
DIA-MS2pep:从数据无关的采集数据中进行全面肽鉴定的无库框架。
由于高度复用的质谱/质谱,直接从数据独立采集(DIA)数据中识别肽仍然具有挑战性。基于谱库的多肽检测灵敏度高,但受限于谱库的深度,抑制了对DIA数据的发现潜力。我们在这里提出DIA- ms2pep,一个从DIA数据中进行全面肽鉴定的无库框架。DIA-MS2pep采用数据驱动算法,使用碎片数据进行MS/MS频谱解复用,而不需要前体。DIA-MS2pep通过对前体质量耐受数据库的搜索,可以识别出肽及其修饰形式。我们通过将DIA- ms2pep与传统的无文库工具进行比较,证明了DIA- ms2pep在肽鉴定的准确性和敏感性方面的性能,这些工具使用了公开的DIA数据集,包括HeLa细胞裂解物、磷酸肽、血浆等。与基于数据依赖获取的光谱库相比,使用DIA- ms2pep直接从DIA数据构建的光谱库提高了定量蛋白质组的准确性和可重复性。
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 去求助
来源期刊
CiteScore
1.30
自引率
0.00%
发文量
117
期刊最新文献
Multi-phase separation in mitochondrial nucleoids and eukaryotic nuclei. Synergistic glycolysis disturbance for cancer therapy by a MOF-based nanospoiler. M6A RNA methylation modification and tumor immune microenvironment in lung adenocarcinoma. Antioxidant activity of the thioredoxin system. The risk model construction of the genes regulated by H3K36me3 and H3K79me2 in breast cancer.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1