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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.
Affiliation
  • Searle BC; Department of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA; Pelotonia Institute for Immuno-Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA. Electronic address: brian.searle@osumc.edu.
  • Chien A; Mass Spectrometry Center, Stanford University, Stanford, California, USA.
  • Koller A; YatiriBio, San Diego, California, USA.
  • Hawke D; BreakBio Corp, New York, New York, USA.
  • Herren AW; UC Davis Genome Center, Proteomics Core, University of California Davis, Davis California, USA.
  • Kim Kim J; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York, USA.
  • Lee KA; Cell Signaling Technology, Inc, Danvers, Massachusetts, USA.
  • Leib RD; Mass Spectrometry Center, Stanford University, Stanford, California, USA.
  • Nelson AJ; Cell Signaling Technology, Inc, Danvers, Massachusetts, USA.
  • Patel P; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, New York, USA.
  • Ren JM; Cell Signaling Technology, Inc, Danvers, Massachusetts, USA.
  • Stemmer PM; Department of Pharmaceutical Sciences, Wayne State University, Detroit, Michigan, USA.
  • Zhu Y; Cell Signaling Technology, Inc, Danvers, Massachusetts, USA.
  • Neely BA; National Institute of Standards and Technology, Charleston, South Carolina, USA.
  • Patel B; Thermo Fisher Scientific, Rockford, Illinois, USA.
Mol Cell Proteomics ; 22(10): 100639, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37657519
ABSTRACT
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphopeptides / Proto-Oncogene Proteins c-akt Language: En Journal: Mol Cell Proteomics Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2023 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphopeptides / Proto-Oncogene Proteins c-akt Language: En Journal: Mol Cell Proteomics Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2023 Type: Article