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Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts

A novel open tubular nanoproteomic platform featuring accelerated on-line protein digestion and high-resolution nano liquid chromatography mass spectrometry (LC-MS) has been developed. The platform features very narrow open tubular columns, and is hence particularly suited for limited sample amounts...

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Autores principales: Hustoft, Hanne Kolsrud, Vehus, Tore, Brandtzaeg, Ole Kristian, Krauss, Stefan, Greibrokk, Tyge, Wilson, Steven Ray, Lundanes, Elsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164520/
https://www.ncbi.nlm.nih.gov/pubmed/25222838
http://dx.doi.org/10.1371/journal.pone.0106881
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author Hustoft, Hanne Kolsrud
Vehus, Tore
Brandtzaeg, Ole Kristian
Krauss, Stefan
Greibrokk, Tyge
Wilson, Steven Ray
Lundanes, Elsa
author_facet Hustoft, Hanne Kolsrud
Vehus, Tore
Brandtzaeg, Ole Kristian
Krauss, Stefan
Greibrokk, Tyge
Wilson, Steven Ray
Lundanes, Elsa
author_sort Hustoft, Hanne Kolsrud
collection PubMed
description A novel open tubular nanoproteomic platform featuring accelerated on-line protein digestion and high-resolution nano liquid chromatography mass spectrometry (LC-MS) has been developed. The platform features very narrow open tubular columns, and is hence particularly suited for limited sample amounts. For enzymatic digestion of proteins, samples are passed through a 20 µm inner diameter (ID) trypsin + endoproteinase Lys-C immobilized open tubular enzyme reactor (OTER). Resulting peptides are subsequently trapped on a monolithic pre-column and transferred on-line to a 10 µm ID porous layer open tubular (PLOT) liquid chromatography LC separation column. Wnt/ß-catenein signaling pathway (Wnt-pathway) proteins of potentially diagnostic value were digested+detected in targeted-MS/MS mode in small cell samples and tumor tissues within 120 minutes. For example, a potential biomarker Axin1 was identifiable in just 10 ng of sample (protein extract of ∼1,000 HCT15 colon cancer cells). In comprehensive mode, the current OTER-PLOT set-up could be used to identify approximately 1500 proteins in HCT15 cells using a relatively short digestion+detection cycle (240 minutes), outperforming previously reported on-line digestion/separation systems. The platform is fully automated utilizing common commercial instrumentation and parts, while the reactor and columns are simple to produce and have low carry-over. These initial results point to automated solutions for fast and very sensitive MS based proteomics, especially for samples of limited size.
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spelling pubmed-41645202014-09-19 Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts Hustoft, Hanne Kolsrud Vehus, Tore Brandtzaeg, Ole Kristian Krauss, Stefan Greibrokk, Tyge Wilson, Steven Ray Lundanes, Elsa PLoS One Research Article A novel open tubular nanoproteomic platform featuring accelerated on-line protein digestion and high-resolution nano liquid chromatography mass spectrometry (LC-MS) has been developed. The platform features very narrow open tubular columns, and is hence particularly suited for limited sample amounts. For enzymatic digestion of proteins, samples are passed through a 20 µm inner diameter (ID) trypsin + endoproteinase Lys-C immobilized open tubular enzyme reactor (OTER). Resulting peptides are subsequently trapped on a monolithic pre-column and transferred on-line to a 10 µm ID porous layer open tubular (PLOT) liquid chromatography LC separation column. Wnt/ß-catenein signaling pathway (Wnt-pathway) proteins of potentially diagnostic value were digested+detected in targeted-MS/MS mode in small cell samples and tumor tissues within 120 minutes. For example, a potential biomarker Axin1 was identifiable in just 10 ng of sample (protein extract of ∼1,000 HCT15 colon cancer cells). In comprehensive mode, the current OTER-PLOT set-up could be used to identify approximately 1500 proteins in HCT15 cells using a relatively short digestion+detection cycle (240 minutes), outperforming previously reported on-line digestion/separation systems. The platform is fully automated utilizing common commercial instrumentation and parts, while the reactor and columns are simple to produce and have low carry-over. These initial results point to automated solutions for fast and very sensitive MS based proteomics, especially for samples of limited size. Public Library of Science 2014-09-15 /pmc/articles/PMC4164520/ /pubmed/25222838 http://dx.doi.org/10.1371/journal.pone.0106881 Text en © 2014 Hustoft et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hustoft, Hanne Kolsrud
Vehus, Tore
Brandtzaeg, Ole Kristian
Krauss, Stefan
Greibrokk, Tyge
Wilson, Steven Ray
Lundanes, Elsa
Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title_full Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title_fullStr Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title_full_unstemmed Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title_short Open Tubular Lab-On-Column/Mass Spectrometry for Targeted Proteomics of Nanogram Sample Amounts
title_sort open tubular lab-on-column/mass spectrometry for targeted proteomics of nanogram sample amounts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164520/
https://www.ncbi.nlm.nih.gov/pubmed/25222838
http://dx.doi.org/10.1371/journal.pone.0106881
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