Literature DB >> 27452035

On the Statistical Significance of Compressed Ratios in Isobaric Labeling: A Cross-Platform Comparison.

Ana Martinez-Val1, Fernando Garcia1, Pilar Ximénez-Embún1, Nuria Ibarz1, Eduardo Zarzuela1, Isabel Ruppen1, Shabaz Mohammed2,3, Javier Munoz1.   

Abstract

Isobaric labeling is gaining popularity in proteomics due to its multiplexing capacity. However, copeptide fragmentation introduces a bias that undermines its accuracy. Several strategies have been shown to partially and, in some cases, completely solve this issue. However, it is still not clear how ratio compression affects the ability to identify a protein's change of abundance as statistically significant. Here, by using the "two proteomes" approach (E. coli lysates with fixed 2.5 ratios in the presence or absence of human lysates acting as the background interference) and manipulating isolation width values, we were able to model isobaric data with different levels of accuracy and precision in three types of mass spectrometers: LTQ Orbitrap Velos, Impact, and Q Exactive. We determined the influence of these variables on the statistical significance of the distorted ratios and compared them to the ratios measured without impurities. Our results confirm previous findings1-4 regarding the importance of optimizing acquisition parameters in each instrument in order to minimize interference without compromising precision and identification. We also show that, under these experimental conditions, the inclusion of a second replicate increases statistical sensitivity 2-3-fold and counterbalances to a large extent the issue of ratio compression.

Entities:  

Keywords:  accuracy; iTRAQ; isobar; isobaric labeling; precision; ratio compression; statistical significance

Mesh:

Substances:

Year:  2016        PMID: 27452035     DOI: 10.1021/acs.jproteome.6b00151

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  4 in total

1.  Benchmarking common quantification strategies for large-scale phosphoproteomics.

Authors:  Alexander Hogrebe; Louise von Stechow; Dorte B Bekker-Jensen; Brian T Weinert; Christian D Kelstrup; Jesper V Olsen
Journal:  Nat Commun       Date:  2018-03-13       Impact factor: 14.919

2.  MSstatsTMT: Statistical Detection of Differentially Abundant Proteins in Experiments with Isobaric Labeling and Multiple Mixtures.

Authors:  Ting Huang; Meena Choi; Manuel Tzouros; Sabrina Golling; Nikhil Janak Pandya; Balazs Banfai; Tom Dunkley; Olga Vitek
Journal:  Mol Cell Proteomics       Date:  2020-07-17       Impact factor: 5.911

Review 3.  Stoichiometric Thiol Redox Proteomics for Quantifying Cellular Responses to Perturbations.

Authors:  Nicholas J Day; Matthew J Gaffrey; Wei-Jun Qian
Journal:  Antioxidants (Basel)       Date:  2021-03-23

4.  PUMILIO proteins promote colorectal cancer growth via suppressing p21.

Authors:  Yuanyuan Gong; Zukai Liu; Yihang Yuan; Zhenzhen Yang; Jiawei Zhang; Qin Lu; Wei Wang; Chao Fang; Haifan Lin; Sanhong Liu
Journal:  Nat Commun       Date:  2022-03-25       Impact factor: 17.694

  4 in total

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