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Automated Enrichment of Phosphotyrosine Peptides for High-Throughput Proteomics.
Chang, Alexis; Leutert, Mario; Rodriguez-Mias, Ricard A; Villén, Judit.
Afiliação
  • Chang A; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, United States.
  • Leutert M; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, United States.
  • Rodriguez-Mias RA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, United States.
  • Villén J; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, United States.
J Proteome Res ; 22(6): 1868-1880, 2023 06 02.
Article em En | MEDLINE | ID: mdl-37097255
Phosphotyrosine (pY) enrichment is critical for expanding the fundamental and clinical understanding of cellular signaling by mass spectrometry-based proteomics. However, current pY enrichment methods exhibit a high cost per sample and limited reproducibility due to expensive affinity reagents and manual processing. We present rapid-robotic phosphotyrosine proteomics (R2-pY), which uses a magnetic particle processor and pY superbinders or antibodies. R2-pY can handle up to 96 samples in parallel, requires 2 days to go from cell lysate to mass spectrometry injections, and results in global proteomic, phosphoproteomic, and tyrosine-specific phosphoproteomic samples. We benchmark the method on HeLa cells stimulated with pervanadate and serum and report over 4000 unique pY sites from 1 mg of peptide input, strong reproducibility between replicates, and phosphopeptide enrichment efficiencies above 99%. R2-pY extends our previously reported R2-P2 proteomic and global phosphoproteomic sample preparation framework, opening the door to large-scale studies of pY signaling in concert with global proteome and phosphoproteome profiling.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Proteômica Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: J Proteome Res Assunto da revista: BIOQUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Proteômica Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: J Proteome Res Assunto da revista: BIOQUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos