How to use open-pFind in deep proteomics data analysis?- A protocol for rigorous identification and quantitation of peptides and proteins from mass spectrometry data.

Guangcan Shao, Yong Cao, Zhenlin Chen, Chao Liu, Shangtong Li, Hao Chi, Meng-Qiu Dong
{"title":"How to use open-pFind in deep proteomics data analysis?- A protocol for rigorous identification and quantitation of peptides and proteins from mass spectrometry data.","authors":"Guangcan Shao,&nbsp;Yong Cao,&nbsp;Zhenlin Chen,&nbsp;Chao Liu,&nbsp;Shangtong Li,&nbsp;Hao Chi,&nbsp;Meng-Qiu Dong","doi":"10.52601/bpr.2021.210004","DOIUrl":null,"url":null,"abstract":"<p><p>High-throughput proteomics based on mass spectrometry (MS) analysis has permeated biomedical science and propelled numerous research projects. pFind 3 is a database search engine for high-speed and in-depth proteomics data analysis. pFind 3 features a swift open search workflow that is adept at uncovering less obvious information such as unexpected modifications or mutations that would have gone unnoticed using a conventional data analysis pipeline. In this protocol, we provide step-by-step instructions to help users mastering various types of data analysis using pFind 3 in conjunction with pParse for data pre-processing and if needed, pQuant for quantitation. This streamlined pParse-pFind-pQuant workflow offers exceptional sensitivity, precision, and speed. It can be easily implemented in any laboratory in need of identifying peptides, proteins, or post-translational modifications, or of quantitation based on <sup>15</sup>N-labeling, SILAC-labeling, or TMT/iTRAQ labeling.</p>","PeriodicalId":59621,"journal":{"name":"生物物理学报:英文版","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244800/pdf/","citationCount":"10","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.2021.210004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

High-throughput proteomics based on mass spectrometry (MS) analysis has permeated biomedical science and propelled numerous research projects. pFind 3 is a database search engine for high-speed and in-depth proteomics data analysis. pFind 3 features a swift open search workflow that is adept at uncovering less obvious information such as unexpected modifications or mutations that would have gone unnoticed using a conventional data analysis pipeline. In this protocol, we provide step-by-step instructions to help users mastering various types of data analysis using pFind 3 in conjunction with pParse for data pre-processing and if needed, pQuant for quantitation. This streamlined pParse-pFind-pQuant workflow offers exceptional sensitivity, precision, and speed. It can be easily implemented in any laboratory in need of identifying peptides, proteins, or post-translational modifications, or of quantitation based on 15N-labeling, SILAC-labeling, or TMT/iTRAQ labeling.

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
如何在深度蛋白质组学数据分析中使用open-pFind ?-从质谱数据中严格鉴定和定量肽和蛋白质的协议。
基于质谱(MS)分析的高通量蛋白质组学已经渗透到生物医学科学中,并推动了许多研究项目。pFind 3是一个用于高速和深入蛋白质组学数据分析的数据库搜索引擎。pFind 3提供了一个快速开放的搜索工作流,它擅长发现不太明显的信息,比如使用传统的数据分析管道无法注意到的意外修改或突变。在本协议中,我们提供分步说明,帮助用户掌握各种类型的数据分析,使用pFind 3与pParse结合进行数据预处理,如果需要,使用pQuant进行定量。这种精简的pParse-pFind-pQuant工作流程提供了卓越的灵敏度,精度和速度。它可以在任何需要鉴定肽,蛋白质或翻译后修饰的实验室中轻松实现,或基于15n标记,silac标记或TMT/iTRAQ标记的定量。
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