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Phosphoproteomics Sample Preparation Impacts Biological Interpretation of Phosphorylation Signaling Outcomes
by
Sampadi, B.
, Mullenders, L.H.F.
, Vrieling, H.
in
Acids
/ Amino Acid Motifs
/ Animals
/ Cell Line
/ cell signaling
/ Chromatography
/ Cytology
/ DNA damage
/ DNA damage response
/ Embryo cells
/ Enzymes
/ Experiments
/ Fractionation
/ high throughput phosphoproteomics
/ high throughput phosphoproteomics; protein phosphorylation; signal transduction; DNA damage response; cell signaling; stress response; ionizing radiation; strong cation exchange chromatography
/ Ionizing radiation
/ Isotope Labeling
/ Kinases
/ Mice
/ Peptides
/ Phosphatase
/ Phosphoproteins
/ Phosphoproteins - chemistry
/ Phosphoproteins - metabolism
/ Phosphoproteomes
/ Phosphorylation
/ protein phosphorylation
/ Proteins
/ Proteome
/ Proteome - metabolism
/ Proteomics
/ QH573-671
/ Radiation
/ Signal Transduction
/ Stem cells
/ stress response
/ strong cation exchange chromatography
2021
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Phosphoproteomics Sample Preparation Impacts Biological Interpretation of Phosphorylation Signaling Outcomes
by
Sampadi, B.
, Mullenders, L.H.F.
, Vrieling, H.
in
Acids
/ Amino Acid Motifs
/ Animals
/ Cell Line
/ cell signaling
/ Chromatography
/ Cytology
/ DNA damage
/ DNA damage response
/ Embryo cells
/ Enzymes
/ Experiments
/ Fractionation
/ high throughput phosphoproteomics
/ high throughput phosphoproteomics; protein phosphorylation; signal transduction; DNA damage response; cell signaling; stress response; ionizing radiation; strong cation exchange chromatography
/ Ionizing radiation
/ Isotope Labeling
/ Kinases
/ Mice
/ Peptides
/ Phosphatase
/ Phosphoproteins
/ Phosphoproteins - chemistry
/ Phosphoproteins - metabolism
/ Phosphoproteomes
/ Phosphorylation
/ protein phosphorylation
/ Proteins
/ Proteome
/ Proteome - metabolism
/ Proteomics
/ QH573-671
/ Radiation
/ Signal Transduction
/ Stem cells
/ stress response
/ strong cation exchange chromatography
2021
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Phosphoproteomics Sample Preparation Impacts Biological Interpretation of Phosphorylation Signaling Outcomes
by
Sampadi, B.
, Mullenders, L.H.F.
, Vrieling, H.
in
Acids
/ Amino Acid Motifs
/ Animals
/ Cell Line
/ cell signaling
/ Chromatography
/ Cytology
/ DNA damage
/ DNA damage response
/ Embryo cells
/ Enzymes
/ Experiments
/ Fractionation
/ high throughput phosphoproteomics
/ high throughput phosphoproteomics; protein phosphorylation; signal transduction; DNA damage response; cell signaling; stress response; ionizing radiation; strong cation exchange chromatography
/ Ionizing radiation
/ Isotope Labeling
/ Kinases
/ Mice
/ Peptides
/ Phosphatase
/ Phosphoproteins
/ Phosphoproteins - chemistry
/ Phosphoproteins - metabolism
/ Phosphoproteomes
/ Phosphorylation
/ protein phosphorylation
/ Proteins
/ Proteome
/ Proteome - metabolism
/ Proteomics
/ QH573-671
/ Radiation
/ Signal Transduction
/ Stem cells
/ stress response
/ strong cation exchange chromatography
2021
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Phosphoproteomics Sample Preparation Impacts Biological Interpretation of Phosphorylation Signaling Outcomes
Journal Article
Phosphoproteomics Sample Preparation Impacts Biological Interpretation of Phosphorylation Signaling Outcomes
2021
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Overview
The influence of phosphoproteomics sample preparation methods on the biological interpretation of signaling outcome is unclear. Here, we demonstrate a strong bias in phosphorylation signaling targets uncovered by comparing the phosphoproteomes generated by two commonly used methods—strong cation exchange chromatography-based phosphoproteomics (SCXPhos) and single-run high-throughput phosphoproteomics (HighPhos). Phosphoproteomes of embryonic stem cells exposed to ionizing radiation (IR) profiled by both methods achieved equivalent coverage (around 20,000 phosphosites), whereas a combined dataset significantly increased the depth (>30,000 phosphosites). While both methods reproducibly quantified a subset of shared IR-responsive phosphosites that represent DNA damage and cell-cycle-related signaling events, most IR-responsive phosphoproteins (>82%) and phosphosites (>96%) were method-specific. Both methods uncovered unique insights into phospho-signaling mediated by single (SCXPhos) versus double/multi-site (HighPhos) phosphorylation events; particularly, each method identified a distinct set of previously unreported IR-responsive kinome/phosphatome (95% disparate) directly impacting the uncovered biology.
Publisher
MDPI AG,MDPI
Subject
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