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A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development

Recent advances in methodology have made phosphopeptide analysis a tractable problem for many proteomics researchers. There are now a wide variety of robust and accessible enrichment strategies to generate phosphoproteomes while free or inexpensive software tools for quantitation and site localizati...

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Autores principales: Searle, Brian C., Chien, Allis, Koller, Antonius, Hawke, David, Herren, Anthony W., Kim Kim, Jenny, Lee, Kimberly A., Leib, Ryan D., Nelson, Alissa J., Patel, Purvi, Ren, Jian Min, Stemmer, Paul M., Zhu, Yiying, Neely, Benjamin A., Patel, Bhavin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561125/
https://www.ncbi.nlm.nih.gov/pubmed/37657519
http://dx.doi.org/10.1016/j.mcpro.2023.100639
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author Searle, Brian C.
Chien, Allis
Koller, Antonius
Hawke, David
Herren, Anthony W.
Kim Kim, Jenny
Lee, Kimberly A.
Leib, Ryan D.
Nelson, Alissa J.
Patel, Purvi
Ren, Jian Min
Stemmer, Paul M.
Zhu, Yiying
Neely, Benjamin A.
Patel, Bhavin
author_facet Searle, Brian C.
Chien, Allis
Koller, Antonius
Hawke, David
Herren, Anthony W.
Kim Kim, Jenny
Lee, Kimberly A.
Leib, Ryan D.
Nelson, Alissa J.
Patel, Purvi
Ren, Jian Min
Stemmer, Paul M.
Zhu, Yiying
Neely, Benjamin A.
Patel, Bhavin
author_sort Searle, Brian C.
collection PubMed
description Recent advances in methodology have made phosphopeptide analysis a tractable problem for many proteomics researchers. There are now a wide variety of robust and accessible enrichment strategies to generate phosphoproteomes while free or inexpensive software tools for quantitation and site localization have simplified phosphoproteome analysis workflow tremendously. As a research group under the Association for Biomolecular Resource Facilities umbrella, the Proteomics Standards Research Group has worked to develop a multipathway phosphopeptide standard based on a mixture of heavy-labeled phosphopeptides designed to enable researchers to rapidly develop assays. This mixture contains 131 mass spectrometry vetted phosphopeptides specifically chosen to cover as many known biologically interesting phosphosites as possible from seven different signaling networks: AMPK signaling, death and apoptosis signaling, ErbB signaling, insulin/insulin-like growth factor-1 signaling, mTOR signaling, PI3K/AKT signaling, and stress (p38/SAPK/JNK) signaling. Here, we describe a characterization of this mixture spiked into a HeLa tryptic digest stimulated with both epidermal growth factor and insulin-like growth factor-1 to activate the MAPK and PI3K/AKT/mTOR pathways. We further demonstrate a comparison of phosphoproteomic profiling of HeLa performed independently in five labs using this phosphopeptide mixture with data-independent acquisition. Despite different experimental and instrumentation processes, we found that labs could produce reproducible, harmonized datasets by reporting measurements as ratios to the standard, while intensity measurements showed lower consistency between labs even after normalization. Our results suggest that widely available, biologically relevant phosphopeptide standards can act as a quantitative “yardstick” across laboratories and sample preparations enabling experimental designs larger than a single laboratory can perform. Raw data files are publicly available in the MassIVE dataset MSV000090564.
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spelling pubmed-105611252023-10-10 A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development Searle, Brian C. Chien, Allis Koller, Antonius Hawke, David Herren, Anthony W. Kim Kim, Jenny Lee, Kimberly A. Leib, Ryan D. Nelson, Alissa J. Patel, Purvi Ren, Jian Min Stemmer, Paul M. Zhu, Yiying Neely, Benjamin A. Patel, Bhavin Mol Cell Proteomics Research Recent advances in methodology have made phosphopeptide analysis a tractable problem for many proteomics researchers. There are now a wide variety of robust and accessible enrichment strategies to generate phosphoproteomes while free or inexpensive software tools for quantitation and site localization have simplified phosphoproteome analysis workflow tremendously. As a research group under the Association for Biomolecular Resource Facilities umbrella, the Proteomics Standards Research Group has worked to develop a multipathway phosphopeptide standard based on a mixture of heavy-labeled phosphopeptides designed to enable researchers to rapidly develop assays. This mixture contains 131 mass spectrometry vetted phosphopeptides specifically chosen to cover as many known biologically interesting phosphosites as possible from seven different signaling networks: AMPK signaling, death and apoptosis signaling, ErbB signaling, insulin/insulin-like growth factor-1 signaling, mTOR signaling, PI3K/AKT signaling, and stress (p38/SAPK/JNK) signaling. Here, we describe a characterization of this mixture spiked into a HeLa tryptic digest stimulated with both epidermal growth factor and insulin-like growth factor-1 to activate the MAPK and PI3K/AKT/mTOR pathways. We further demonstrate a comparison of phosphoproteomic profiling of HeLa performed independently in five labs using this phosphopeptide mixture with data-independent acquisition. Despite different experimental and instrumentation processes, we found that labs could produce reproducible, harmonized datasets by reporting measurements as ratios to the standard, while intensity measurements showed lower consistency between labs even after normalization. Our results suggest that widely available, biologically relevant phosphopeptide standards can act as a quantitative “yardstick” across laboratories and sample preparations enabling experimental designs larger than a single laboratory can perform. Raw data files are publicly available in the MassIVE dataset MSV000090564. American Society for Biochemistry and Molecular Biology 2023-08-30 /pmc/articles/PMC10561125/ /pubmed/37657519 http://dx.doi.org/10.1016/j.mcpro.2023.100639 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research
Searle, Brian C.
Chien, Allis
Koller, Antonius
Hawke, David
Herren, Anthony W.
Kim Kim, Jenny
Lee, Kimberly A.
Leib, Ryan D.
Nelson, Alissa J.
Patel, Purvi
Ren, Jian Min
Stemmer, Paul M.
Zhu, Yiying
Neely, Benjamin A.
Patel, Bhavin
A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title_full A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title_fullStr A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title_full_unstemmed A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title_short A Multipathway Phosphopeptide Standard for Rapid Phosphoproteomics Assay Development
title_sort multipathway phosphopeptide standard for rapid phosphoproteomics assay development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561125/
https://www.ncbi.nlm.nih.gov/pubmed/37657519
http://dx.doi.org/10.1016/j.mcpro.2023.100639
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