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The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research

Precise quantitation of protein biomarkers in clinical tissue specimens is a prerequisite for accurate and effective diagnosis, prognosis, and personalized medicine. Although progress is being made, protein analysis from formalin-fixed and paraffin-embedded tissues is still challenging. In previous...

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Autores principales: Gündisch, Sibylle, Schott, Christina, Wolff, Claudia, Tran, Kai, Beese, Christian, Viertler, Christian, Zatloukal, Kurt, Becker, Karl-Friedrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612043/
https://www.ncbi.nlm.nih.gov/pubmed/23555997
http://dx.doi.org/10.1371/journal.pone.0060638
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author Gündisch, Sibylle
Schott, Christina
Wolff, Claudia
Tran, Kai
Beese, Christian
Viertler, Christian
Zatloukal, Kurt
Becker, Karl-Friedrich
author_facet Gündisch, Sibylle
Schott, Christina
Wolff, Claudia
Tran, Kai
Beese, Christian
Viertler, Christian
Zatloukal, Kurt
Becker, Karl-Friedrich
author_sort Gündisch, Sibylle
collection PubMed
description Precise quantitation of protein biomarkers in clinical tissue specimens is a prerequisite for accurate and effective diagnosis, prognosis, and personalized medicine. Although progress is being made, protein analysis from formalin-fixed and paraffin-embedded tissues is still challenging. In previous reports, we showed that the novel formalin-free tissue preservation technology, the PAXgene Tissue System, allows the extraction of intact and immunoreactive proteins from PAXgene-fixed and paraffin-embedded (PFPE) tissues. In the current study, we focused on the analysis of phosphoproteins and the applicability of two-dimensional gel electrophoresis (2D-PAGE) and enzyme-linked immunosorbent assay (ELISA) to the analysis of a variety of malignant and non-malignant human tissues. Using western blot analysis, we found that phosphoproteins are quantitatively preserved in PFPE tissues, and signal intensities are comparable to that in paired, frozen tissues. Furthermore, proteins extracted from PFPE samples are suitable for 2D-PAGE and can be quantified by ELISA specific for denatured proteins. In summary, the PAXgene Tissue System reliably preserves phosphoproteins in human tissue samples, even after prolonged fixation or stabilization times, and is compatible with methods for protein analysis such as 2D-PAGE and ELISA. We conclude that the PAXgene Tissue System has the potential to serve as a versatile tissue fixative for modern pathology.
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spelling pubmed-36120432013-04-03 The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research Gündisch, Sibylle Schott, Christina Wolff, Claudia Tran, Kai Beese, Christian Viertler, Christian Zatloukal, Kurt Becker, Karl-Friedrich PLoS One Research Article Precise quantitation of protein biomarkers in clinical tissue specimens is a prerequisite for accurate and effective diagnosis, prognosis, and personalized medicine. Although progress is being made, protein analysis from formalin-fixed and paraffin-embedded tissues is still challenging. In previous reports, we showed that the novel formalin-free tissue preservation technology, the PAXgene Tissue System, allows the extraction of intact and immunoreactive proteins from PAXgene-fixed and paraffin-embedded (PFPE) tissues. In the current study, we focused on the analysis of phosphoproteins and the applicability of two-dimensional gel electrophoresis (2D-PAGE) and enzyme-linked immunosorbent assay (ELISA) to the analysis of a variety of malignant and non-malignant human tissues. Using western blot analysis, we found that phosphoproteins are quantitatively preserved in PFPE tissues, and signal intensities are comparable to that in paired, frozen tissues. Furthermore, proteins extracted from PFPE samples are suitable for 2D-PAGE and can be quantified by ELISA specific for denatured proteins. In summary, the PAXgene Tissue System reliably preserves phosphoproteins in human tissue samples, even after prolonged fixation or stabilization times, and is compatible with methods for protein analysis such as 2D-PAGE and ELISA. We conclude that the PAXgene Tissue System has the potential to serve as a versatile tissue fixative for modern pathology. Public Library of Science 2013-03-29 /pmc/articles/PMC3612043/ /pubmed/23555997 http://dx.doi.org/10.1371/journal.pone.0060638 Text en © 2013 Gündisch 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
Gündisch, Sibylle
Schott, Christina
Wolff, Claudia
Tran, Kai
Beese, Christian
Viertler, Christian
Zatloukal, Kurt
Becker, Karl-Friedrich
The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title_full The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title_fullStr The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title_full_unstemmed The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title_short The PAXgene(®) Tissue System Preserves Phosphoproteins in Human Tissue Specimens and Enables Comprehensive Protein Biomarker Research
title_sort paxgene(®) tissue system preserves phosphoproteins in human tissue specimens and enables comprehensive protein biomarker research
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612043/
https://www.ncbi.nlm.nih.gov/pubmed/23555997
http://dx.doi.org/10.1371/journal.pone.0060638
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