Thousand and one ways to quantify and compare protein abundances in label-free bottom-up proteomics

How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen years. Two main approaches are generally used: the first is based on spectral data generated during the process of identification (e.g. pepti...

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Published inBiochimica et biophysica acta Vol. 1864; no. 8; pp. 883 - 895
Main Authors Blein-Nicolas, Mélisande, Zivy, Michel
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.08.2016
Elsevier
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Abstract How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen years. Two main approaches are generally used: the first is based on spectral data generated during the process of identification (e.g. peptide counting, spectral counting), while the second makes use of extracted ion currents to quantify chromatographic peaks and infer protein abundances based on peptide quantification. These two approaches actually refer to multiple methods which have been developed during the last decade, but were submitted to deep evaluations only recently. In this paper, we compiled these different methods as exhaustively as possible. We also summarized the way they address the different problems raised by bottom-up protein quantification such as normalization, the presence of shared peptides, unequal peptide measurability and missing data. This article is part of a Special Issue entitled: Plant Proteomics— a bridge between fundamental processes and crop production, edited by Dr. Hans-Peter Mock. •Many methods to quantify and compare protein abundances in bottom-up proteomics•Two complementary approaches: identification-based and XIC-based•Identification-based approach is better suited for detection of large abundance variations.•XIC-based approach is more sensitive.•No gold standard method at present
AbstractList How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen years. Two main approaches are generally used: the first is based on spectral data generated during the process of identification (e.g. peptide counting, spectral counting), while the second makes use of extracted ion currents to quantify chromatographic peaks and infer protein abundances based on peptide quantification. These two approaches actually refer to multiple methods which have been developed during the last decade, but were submitted to deep evaluations only recently. In this paper, we compiled these different methods as exhaustively as possible. We also summarized the way they address the different problems raised by bottom-up protein quantification such as normalization, the presence of shared peptides, unequal peptide measurability and missing data. This article is part of a Special Issue entitled: Plant Proteomics--a bridge between fundamental processes and crop production, edited by Dr. Hans-Peter Mock.
How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen years. Two main approaches are generally used: the first is based on spectral data generated during the process of identification (e.g. peptide counting, spectral counting), while the second makes use of extracted ion currents to quantify chromatographic pealcs and infer protein abundances based on peptide quantification. These two approaches actually refer to multiple methods which have been developed during the last decade, but were submitted to deep evaluations only recently. In this paper, we compiled these different methods as exhaustively as possible. We also summarized the way they address the different problems raised by bottom-up protein quantification such as normalization, the presence of shared peptides, unequal peptide measurability and missing data. This article is part of a Special Issue entitled: Plant Proteomics- a bridge between fundamental processes and crop production, edited by Dr. Hans-Peter Mock. (C) 2016 Elsevier B.V. All rights reserved.
How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen years. Two main approaches are generally used: the first is based on spectral data generated during the process of identification (e.g. peptide counting, spectral counting), while the second makes use of extracted ion currents to quantify chromatographic peaks and infer protein abundances based on peptide quantification. These two approaches actually refer to multiple methods which have been developed during the last decade, but were submitted to deep evaluations only recently. In this paper, we compiled these different methods as exhaustively as possible. We also summarized the way they address the different problems raised by bottom-up protein quantification such as normalization, the presence of shared peptides, unequal peptide measurability and missing data. This article is part of a Special Issue entitled: Plant Proteomics— a bridge between fundamental processes and crop production, edited by Dr. Hans-Peter Mock. •Many methods to quantify and compare protein abundances in bottom-up proteomics•Two complementary approaches: identification-based and XIC-based•Identification-based approach is better suited for detection of large abundance variations.•XIC-based approach is more sensitive.•No gold standard method at present
Author Zivy, Michel
Blein-Nicolas, Mélisande
Author_xml – sequence: 1
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  fullname: Zivy, Michel
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Issue 8
Keywords SC
XIC
FDR
Data processing
LC–MS/MS
Mass spectrometry
Statistics
Peptide
TOTAL ION CURRENT
TANDEM MASS-SPECTROMETRY
LC-MS PROTEOMICS
SPECTRAL COUNT DATA
LIQUID-CHROMATOGRAPHY
ABSOLUTE PROTEIN
FREE SHOTGUN PROTEOMICS
DIFFERENTIALLY EXPRESSED GENES
FREE QUANTITATIVE PROTEOMICS
PEPTIDE QUANTIFICATION
Language English
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Snippet How to process and analyze MS data to quantify and statistically compare protein abundances in bottom-up proteomics has been an open debate for nearly fifteen...
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SubjectTerms Crops, Agricultural - chemistry
Crops, Agricultural - metabolism
Data processing
Life Sciences
Mass spectrometry
Mass Spectrometry - methods
Peptide
Peptides - chemistry
Peptides - metabolism
Plant Proteins - analysis
Plant Proteins - metabolism
Proteomics - methods
Statistics
Title Thousand and one ways to quantify and compare protein abundances in label-free bottom-up proteomics
URI https://dx.doi.org/10.1016/j.bbapap.2016.02.019
https://www.ncbi.nlm.nih.gov/pubmed/26947242
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