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HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography

Protein analysis using high-performance thin-layer chromatography (HPTLC) is not commonly used but can complement traditional electrophoretic and mass spectrometric approaches in a unique way. Due to various detection protocols and possibilities for hyphenation, HPTLC protein analysis is a promising...

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Autores principales: Morschheuser, Lena, Wessels, Hauke, Pille, Christina, Fischer, Judith, Hünniger, Tim, Fischer, Markus, Paschke-Kratzin, Angelika, Rohn, Sascha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879557/
https://www.ncbi.nlm.nih.gov/pubmed/27220270
http://dx.doi.org/10.1038/srep26665
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author Morschheuser, Lena
Wessels, Hauke
Pille, Christina
Fischer, Judith
Hünniger, Tim
Fischer, Markus
Paschke-Kratzin, Angelika
Rohn, Sascha
author_facet Morschheuser, Lena
Wessels, Hauke
Pille, Christina
Fischer, Judith
Hünniger, Tim
Fischer, Markus
Paschke-Kratzin, Angelika
Rohn, Sascha
author_sort Morschheuser, Lena
collection PubMed
description Protein analysis using high-performance thin-layer chromatography (HPTLC) is not commonly used but can complement traditional electrophoretic and mass spectrometric approaches in a unique way. Due to various detection protocols and possibilities for hyphenation, HPTLC protein analysis is a promising alternative for e.g., investigating posttranslational modifications. This study exemplarily focused on the investigation of lysozyme, an enzyme which is occurring in eggs and technologically added to foods and beverages such as wine. The detection of lysozyme is mandatory, as it might trigger allergenic reactions in sensitive individuals. To underline the advantages of HPTLC in protein analysis, the development of innovative, highly specific staining protocols leads to improved sensitivity for protein detection on HPTLC plates in comparison to universal protein derivatization reagents. This study aimed at developing a detection methodology for HPTLC separated proteins using aptamers. Due to their affinity and specificity towards a wide range of targets, an aptamer based staining procedure on HPTLC (HPTLC-aptastaining) will enable manifold analytical possibilities. Besides the proof of its applicability for the very first time, (i) aptamer-based staining of proteins is applicable on different stationary phase materials and (ii) furthermore, it can be used as an approach for a semi-quantitative estimation of protein concentrations.
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spelling pubmed-48795572016-06-07 HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography Morschheuser, Lena Wessels, Hauke Pille, Christina Fischer, Judith Hünniger, Tim Fischer, Markus Paschke-Kratzin, Angelika Rohn, Sascha Sci Rep Article Protein analysis using high-performance thin-layer chromatography (HPTLC) is not commonly used but can complement traditional electrophoretic and mass spectrometric approaches in a unique way. Due to various detection protocols and possibilities for hyphenation, HPTLC protein analysis is a promising alternative for e.g., investigating posttranslational modifications. This study exemplarily focused on the investigation of lysozyme, an enzyme which is occurring in eggs and technologically added to foods and beverages such as wine. The detection of lysozyme is mandatory, as it might trigger allergenic reactions in sensitive individuals. To underline the advantages of HPTLC in protein analysis, the development of innovative, highly specific staining protocols leads to improved sensitivity for protein detection on HPTLC plates in comparison to universal protein derivatization reagents. This study aimed at developing a detection methodology for HPTLC separated proteins using aptamers. Due to their affinity and specificity towards a wide range of targets, an aptamer based staining procedure on HPTLC (HPTLC-aptastaining) will enable manifold analytical possibilities. Besides the proof of its applicability for the very first time, (i) aptamer-based staining of proteins is applicable on different stationary phase materials and (ii) furthermore, it can be used as an approach for a semi-quantitative estimation of protein concentrations. Nature Publishing Group 2016-05-25 /pmc/articles/PMC4879557/ /pubmed/27220270 http://dx.doi.org/10.1038/srep26665 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Morschheuser, Lena
Wessels, Hauke
Pille, Christina
Fischer, Judith
Hünniger, Tim
Fischer, Markus
Paschke-Kratzin, Angelika
Rohn, Sascha
HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title_full HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title_fullStr HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title_full_unstemmed HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title_short HPTLC-aptastaining – Innovative protein detection system for high-performance thin-layer chromatography
title_sort hptlc-aptastaining – innovative protein detection system for high-performance thin-layer chromatography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879557/
https://www.ncbi.nlm.nih.gov/pubmed/27220270
http://dx.doi.org/10.1038/srep26665
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