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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2014
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Tape, Christopher J. |
collection | PubMed |
description | [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. |
format | Online Article Text |
id | pubmed-4206527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42065272014-10-27 Reproducible Automated Phosphopeptide Enrichment Using Magnetic TiO(2) and Ti-IMAC 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 Anal Chem [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. American Chemical Society 2014-09-18 2014-10-21 /pmc/articles/PMC4206527/ /pubmed/25233145 http://dx.doi.org/10.1021/ac5025842 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | 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 Reproducible Automated Phosphopeptide Enrichment Using Magnetic TiO(2) and Ti-IMAC |
title | Reproducible Automated Phosphopeptide Enrichment Using
Magnetic TiO(2) and Ti-IMAC |
title_full | Reproducible Automated Phosphopeptide Enrichment Using
Magnetic TiO(2) and Ti-IMAC |
title_fullStr | Reproducible Automated Phosphopeptide Enrichment Using
Magnetic TiO(2) and Ti-IMAC |
title_full_unstemmed | Reproducible Automated Phosphopeptide Enrichment Using
Magnetic TiO(2) and Ti-IMAC |
title_short | Reproducible Automated Phosphopeptide Enrichment Using
Magnetic TiO(2) and Ti-IMAC |
title_sort | reproducible automated phosphopeptide enrichment using
magnetic tio(2) and ti-imac |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206527/ https://www.ncbi.nlm.nih.gov/pubmed/25233145 http://dx.doi.org/10.1021/ac5025842 |
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