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Reproducible Automated Phosphopeptide Enrichment Using Magnetic TiO(2) and Ti-IMAC

[Image: see text] Reproducible, comprehensive phosphopeptide enrichment is essential for studying phosphorylation-regulated processes. Here, we describe the application of hyper-porous magnetic TiO(2) and Ti-IMAC microspheres for uniform automated phosphopeptide enrichment. Combining magnetic micros...

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Detalles Bibliográficos
Autores principales: Tape, Christopher J., Worboys, Jonathan D., Sinclair, John, Gourlay, Robert, Vogt, Janis, McMahon, Kelly M., Trost, Matthias, Lauffenburger, Douglas A., Lamont, Douglas J., Jørgensen, Claus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206527/
https://www.ncbi.nlm.nih.gov/pubmed/25233145
http://dx.doi.org/10.1021/ac5025842
Descripción
Sumario:[Image: see text] Reproducible, comprehensive phosphopeptide enrichment is essential for studying phosphorylation-regulated processes. Here, we describe the application of hyper-porous magnetic TiO(2) and Ti-IMAC microspheres for uniform automated phosphopeptide enrichment. Combining magnetic microspheres with a magnetic particle-handling robot enables rapid (45 min), reproducible (r2 ≥ 0.80) and high-fidelity (>90% purity) phosphopeptide purification in a 96-well format. Automated phosphopeptide enrichment demonstrates reproducible synthetic phosphopeptide recovery across 2 orders of magnitude, “well-to-well” quantitative reproducibility indistinguishable to internal SILAC standards, and robust “plate-to-plate” reproducibility across 5 days of independent enrichments. As a result, automated phosphopeptide enrichment enables statistical analysis of label-free phosphoproteomic samples in a high-throughput manner. This technique uses commercially available, off-the-shelf components and can be easily adopted by any laboratory interested in phosphoproteomic analysis. We provide a free downloadable automated phosphopeptide enrichment program to facilitate uniform interlaboratory collaboration and exchange of phosphoproteomic data sets.