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Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics
AIM: We compared four commonly used, commercially available reverse phase nanoLC columns for identification/determination of Wnt/β-catenin-related pathway proteins. MATERIALS & METHODS: The columns were: Chromolith(®) (silica monolith; Merke Millipore, MA, USA), PepMap™ (porous particles; Thermo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137844/ https://www.ncbi.nlm.nih.gov/pubmed/28031966 http://dx.doi.org/10.4155/fsoa-2016-0014 |
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author | Vehus, Tore Seterdal, Kristina Erikstad Krauss, Stefan Lundanes, Elsa Wilson, Steven R |
author_facet | Vehus, Tore Seterdal, Kristina Erikstad Krauss, Stefan Lundanes, Elsa Wilson, Steven R |
author_sort | Vehus, Tore |
collection | PubMed |
description | AIM: We compared four commonly used, commercially available reverse phase nanoLC columns for identification/determination of Wnt/β-catenin-related pathway proteins. MATERIALS & METHODS: The columns were: Chromolith(®) (silica monolith; Merke Millipore, MA, USA), PepMap™ (porous particles; Thermo Fisher Scientific, MA, USA), Accucore™ (solid core particles; Thermo Fisher Scientific) and PepSwift™ (organic monolith; Thermo Fisher Scientific). RESULTS: The peak capacity of the columns varied from 100 (Pepswift) to 190 (Accucore) (for 30 min gradients). All columns enabled identification/detection of GSK3β and β-catenin in the complex samples. However, even the columns with higher peak capacities could not enable detection of the somewhat less abundant proteins AXIN2 and TNKS2. The monoliths were more prone to retention time instability when sample complexity increased. CONCLUSION: We find that commercial nanoLC columns, although featuring different morphologies and peak capacities, provided surprisingly few practical differences for relatively fast, targeted determination of proteins. |
format | Online Article Text |
id | pubmed-5137844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51378442016-12-28 Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics Vehus, Tore Seterdal, Kristina Erikstad Krauss, Stefan Lundanes, Elsa Wilson, Steven R Future Sci OA Research Article AIM: We compared four commonly used, commercially available reverse phase nanoLC columns for identification/determination of Wnt/β-catenin-related pathway proteins. MATERIALS & METHODS: The columns were: Chromolith(®) (silica monolith; Merke Millipore, MA, USA), PepMap™ (porous particles; Thermo Fisher Scientific, MA, USA), Accucore™ (solid core particles; Thermo Fisher Scientific) and PepSwift™ (organic monolith; Thermo Fisher Scientific). RESULTS: The peak capacity of the columns varied from 100 (Pepswift) to 190 (Accucore) (for 30 min gradients). All columns enabled identification/detection of GSK3β and β-catenin in the complex samples. However, even the columns with higher peak capacities could not enable detection of the somewhat less abundant proteins AXIN2 and TNKS2. The monoliths were more prone to retention time instability when sample complexity increased. CONCLUSION: We find that commercial nanoLC columns, although featuring different morphologies and peak capacities, provided surprisingly few practical differences for relatively fast, targeted determination of proteins. Future Science Ltd 2016-03-16 /pmc/articles/PMC5137844/ /pubmed/28031966 http://dx.doi.org/10.4155/fsoa-2016-0014 Text en © Tore Vehus This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Article Vehus, Tore Seterdal, Kristina Erikstad Krauss, Stefan Lundanes, Elsa Wilson, Steven R Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title | Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title_full | Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title_fullStr | Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title_full_unstemmed | Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title_short | Comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
title_sort | comparison of commercial nanoliquid chromatography columns for fast, targeted mass spectrometry-based proteomics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137844/ https://www.ncbi.nlm.nih.gov/pubmed/28031966 http://dx.doi.org/10.4155/fsoa-2016-0014 |
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