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 in | Biochimica et biophysica acta Vol. 1864; no. 8; pp. 883 - 895 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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 |
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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 givenname: Mélisande surname: Blein-Nicolas fullname: Blein-Nicolas, Mélisande – sequence: 2 givenname: Michel surname: Zivy fullname: Zivy, Michel email: zivy@moulon.inra.fr |
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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 |
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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 |
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