• 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

A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.

作者信息

Zhu Qi, Kasim Adetayo, Valkenborg Dirk, Burzykowski Tomasz

机构信息

Department of Electrical Engineering, ESAT/SCD Katholieke Universiteit Leuven, Kasteelpark Arenberg 10, Bus 2446, 3001 Heverlee, Belgium.

出版信息

Int J Proteomics. 2011;2011:928391. doi: 10.1155/2011/928391. Epub 2011 May 23.

DOI:10.1155/2011/928391
PMID:22091391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3200211/
Abstract

In a high-resolution MALDI-TOF mass spectrum, a peptide produces multiple peaks, corresponding to the isotopic variants of the molecules. An overlap occurs when two peptides appear in the vicinity of the mass coordinate, resulting in the difficulty of quantifying the relative abundance and the exact masses of these peptides. To address the problem, two factors need to be considered: (1) the variability pertaining to the abundances of the isotopic variants (2) extra information content needed to supplement the information contained in data. We propose a Bayesian model for the incorporation of prior information. Such information exists, for example, for the distribution of the masses of peptides and the abundances of the isotopic variants. The model we develop allows for the correct estimation of the parameters of interest. The validity of the modeling approach is verified by a real-life case study from a controlled mass spectrometry experiment and by a simulation study.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/4407ecc18700/IJPRO2011-928391.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/423054732e56/IJPRO2011-928391.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/092631fec624/IJPRO2011-928391.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/7183ba1ce7fe/IJPRO2011-928391.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/b9a852771046/IJPRO2011-928391.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/1adc2354af27/IJPRO2011-928391.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/77b33c9de893/IJPRO2011-928391.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/f79caab1c5a5/IJPRO2011-928391.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/db286316ef32/IJPRO2011-928391.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/ab6fe51d9032/IJPRO2011-928391.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/4407ecc18700/IJPRO2011-928391.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/423054732e56/IJPRO2011-928391.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/092631fec624/IJPRO2011-928391.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/7183ba1ce7fe/IJPRO2011-928391.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/b9a852771046/IJPRO2011-928391.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/1adc2354af27/IJPRO2011-928391.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/77b33c9de893/IJPRO2011-928391.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/f79caab1c5a5/IJPRO2011-928391.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/db286316ef32/IJPRO2011-928391.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/ab6fe51d9032/IJPRO2011-928391.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c28/3200211/4407ecc18700/IJPRO2011-928391.010.jpg

相似文献

1
A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.
Int J Proteomics. 2011;2011:928391. doi: 10.1155/2011/928391. Epub 2011 May 23.
2
Quality control based on isotopic distributions for high-throughput MALDI-TOF and MALDI-FTICR serum peptide profiling.基于同位素分布的高通量 MALDI-TOF 和 MALDI-FTICR 血清肽谱的质量控制。
J Am Soc Mass Spectrom. 2010 Sep;21(9):1515-25. doi: 10.1016/j.jasms.2010.05.004. Epub 2010 May 12.
3
Quantification of isotopically overlapping deamidated and 18o-labeled peptides using isotopic envelope mixture modeling.使用同位素包络混合物建模对同位素重叠的脱酰胺化和18O标记肽进行定量。
J Proteome Res. 2009 Mar;8(3):1263-70. doi: 10.1021/pr801054w.
4
Quantifying peptide signal in MALDI-TOF mass spectrometry data.
Mol Cell Proteomics. 2005 Dec;4(12):1990-9. doi: 10.1074/mcp.M500130-MCP200. Epub 2005 Sep 29.
5
A strategy for the prior processing of high-resolution mass spectral data obtained from high-dimensional combined fractional diagonal chromatography.一种用于对从高维组合分数对角色谱法获得的高分辨率质谱数据进行预处理的策略。
J Mass Spectrom. 2009 Apr;44(4):516-29. doi: 10.1002/jms.1527.
6
Deconvolution of overlapping isotopic clusters improves quantification of stable isotope-labeled peptides.重叠同位素峰的解卷积可提高稳定同位素标记肽的定量分析。
J Proteomics. 2011 Sep 6;74(10):2204-9. doi: 10.1016/j.jprot.2011.04.022. Epub 2011 May 15.
7
QUDeX-MS: hydrogen/deuterium exchange calculation for mass spectra with resolved isotopic fine structure.QUDeX-MS:用于具有分辨同位素精细结构的质谱的氢/氘交换计算
BMC Bioinformatics. 2014 Dec 11;15(1):403. doi: 10.1186/s12859-014-0403-1.
8
The MALDI-TOF mass spectrometric view of the plasma proteome and peptidome.血浆蛋白质组和肽组的基质辅助激光解吸电离飞行时间质谱图。
Clin Chem. 2006 Jul;52(7):1223-37. doi: 10.1373/clinchem.2006.069252. Epub 2006 Apr 27.
9
A model-based method for the prediction of the isotopic distribution of peptides.一种基于模型的预测肽同位素分布的方法。
J Am Soc Mass Spectrom. 2008 May;19(5):703-12. doi: 10.1016/j.jasms.2008.01.009. Epub 2008 Jan 31.
10
A study of the properties of Gaussian mixture model for stable isotope standard quantification in MALDI-TOF MS.用于基质辅助激光解吸电离飞行时间质谱中稳定同位素标准定量的高斯混合模型特性研究
Commun Stat Simul Comput. 2019;48(6):1637-1650. doi: 10.1080/03610918.2017.1422748. Epub 2018 Jan 30.

引用本文的文献

1
Accurate LC peak boundary detection for ¹⁶O/¹⁸O labeled LC-MS data.准确检测¹⁶O/¹⁸O 标记 LC-MS 数据的 LC 峰边界。
PLoS One. 2013 Oct 7;8(10):e72951. doi: 10.1371/journal.pone.0072951. eCollection 2013.

本文引用的文献

1
Markov-chain-based heteroscedastic regression model for the analysis of high-resolution enzymatically 18O-labeled mass spectra.基于马尔可夫链的异方差回归模型分析高分辨率酶法 18O 标记质谱。
J Proteome Res. 2010 May 7;9(5):2669-77. doi: 10.1021/pr100169a.
2
A strategy for the prior processing of high-resolution mass spectral data obtained from high-dimensional combined fractional diagonal chromatography.一种用于对从高维组合分数对角色谱法获得的高分辨率质谱数据进行预处理的策略。
J Mass Spectrom. 2009 Apr;44(4):516-29. doi: 10.1002/jms.1527.
3
A model-based method for the prediction of the isotopic distribution of peptides.
一种基于模型的预测肽同位素分布的方法。
J Am Soc Mass Spectrom. 2008 May;19(5):703-12. doi: 10.1016/j.jasms.2008.01.009. Epub 2008 Jan 31.
4
High-accuracy peak picking of proteomics data using wavelet techniques.使用小波技术对蛋白质组学数据进行高精度峰检测。
Pac Symp Biocomput. 2006:243-54.
5
Proteolytic 18O-labeling strategies for quantitative proteomics.用于定量蛋白质组学的蛋白水解18O标记策略。
Mass Spectrom Rev. 2007 Jan-Feb;26(1):121-36. doi: 10.1002/mas.20116.
6
Regression analysis for comparing protein samples with 16O/18O stable-isotope labeled mass spectrometry.使用16O/18O稳定同位素标记质谱法比较蛋白质样品的回归分析。
Bioinformatics. 2006 Nov 15;22(22):2739-45. doi: 10.1093/bioinformatics/btl464. Epub 2006 Sep 5.
7
Automatic poisson peak harvesting for high throughput protein identification.用于高通量蛋白质鉴定的自动泊松峰采集
Electrophoresis. 2000 Jun;21(11):2243-51. doi: 10.1002/1522-2683(20000601)21:11<2243::AID-ELPS2243>3.0.CO;2-K.
8
Modeling peptide mass fingerprinting data using the atomic composition of peptides.
Electrophoresis. 1999 Dec;20(18):3527-34. doi: 10.1002/(SICI)1522-2683(19991201)20:18<3527::AID-ELPS3527>3.0.CO;2-9.