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Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins

Direct tissue imaging mass spectrometry (IMS) by matrix-assisted laser desorption ionization and time-of-flight (MALDI-TOF) mass spectrometry has become increasingly important in biology and medicine, because this technology can detect the relative abundance and spatial distribution of interesting p...

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Autores principales: Min, Kyueng-Whan, Bang, Joo-Young, Kim, Kwang Pyo, Kim, Wan-Seop, Lee, Sang Hwa, Shanta, Selina Rahman, Lee, Jeong Hwa, Hong, Ji Hye, Lim, So Dug, Yoo, Young-Bum, Na, Chan-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101781/
https://www.ncbi.nlm.nih.gov/pubmed/25045225
http://dx.doi.org/10.3346/jkms.2014.29.7.934
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author Min, Kyueng-Whan
Bang, Joo-Young
Kim, Kwang Pyo
Kim, Wan-Seop
Lee, Sang Hwa
Shanta, Selina Rahman
Lee, Jeong Hwa
Hong, Ji Hye
Lim, So Dug
Yoo, Young-Bum
Na, Chan-Hyun
author_facet Min, Kyueng-Whan
Bang, Joo-Young
Kim, Kwang Pyo
Kim, Wan-Seop
Lee, Sang Hwa
Shanta, Selina Rahman
Lee, Jeong Hwa
Hong, Ji Hye
Lim, So Dug
Yoo, Young-Bum
Na, Chan-Hyun
author_sort Min, Kyueng-Whan
collection PubMed
description Direct tissue imaging mass spectrometry (IMS) by matrix-assisted laser desorption ionization and time-of-flight (MALDI-TOF) mass spectrometry has become increasingly important in biology and medicine, because this technology can detect the relative abundance and spatial distribution of interesting proteins in tissues. Five thyroid cancer samples, along with normal tissue, were sliced and transferred onto conductive glass slides. After laser scanning by MALDI-TOF equipped with a smart beam laser, images were created for individual masses and proteins were classified at 200-µm spatial resolution. Based on the spatial distribution, region-specific proteins on a tumor lesion could be identified by protein extraction from tumor tissue and analysis using liquid chromatography with tandem mass spectrometry (LC-MS/MS). Using all the spectral data at each spot, various intensities of a specific peak were detected in the tumor and normal regions of the thyroid. Differences in the molecular weights of expressed proteins between tumor and normal regions were analyzed using unsupervised and supervised clustering. To verify the presence of discovered proteins through IMS, we identified ribosomal protein P2, which is specific for cancer. We have demonstrated the feasibility of IMS as a useful tool for the analysis of tissue sections, and identified the tumor-specific protein ribosomal protein P2. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-41017812014-07-18 Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins Min, Kyueng-Whan Bang, Joo-Young Kim, Kwang Pyo Kim, Wan-Seop Lee, Sang Hwa Shanta, Selina Rahman Lee, Jeong Hwa Hong, Ji Hye Lim, So Dug Yoo, Young-Bum Na, Chan-Hyun J Korean Med Sci Original Article Direct tissue imaging mass spectrometry (IMS) by matrix-assisted laser desorption ionization and time-of-flight (MALDI-TOF) mass spectrometry has become increasingly important in biology and medicine, because this technology can detect the relative abundance and spatial distribution of interesting proteins in tissues. Five thyroid cancer samples, along with normal tissue, were sliced and transferred onto conductive glass slides. After laser scanning by MALDI-TOF equipped with a smart beam laser, images were created for individual masses and proteins were classified at 200-µm spatial resolution. Based on the spatial distribution, region-specific proteins on a tumor lesion could be identified by protein extraction from tumor tissue and analysis using liquid chromatography with tandem mass spectrometry (LC-MS/MS). Using all the spectral data at each spot, various intensities of a specific peak were detected in the tumor and normal regions of the thyroid. Differences in the molecular weights of expressed proteins between tumor and normal regions were analyzed using unsupervised and supervised clustering. To verify the presence of discovered proteins through IMS, we identified ribosomal protein P2, which is specific for cancer. We have demonstrated the feasibility of IMS as a useful tool for the analysis of tissue sections, and identified the tumor-specific protein ribosomal protein P2. GRAPHICAL ABSTRACT: [Image: see text] The Korean Academy of Medical Sciences 2014-07 2014-07-11 /pmc/articles/PMC4101781/ /pubmed/25045225 http://dx.doi.org/10.3346/jkms.2014.29.7.934 Text en © 2014 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Min, Kyueng-Whan
Bang, Joo-Young
Kim, Kwang Pyo
Kim, Wan-Seop
Lee, Sang Hwa
Shanta, Selina Rahman
Lee, Jeong Hwa
Hong, Ji Hye
Lim, So Dug
Yoo, Young-Bum
Na, Chan-Hyun
Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title_full Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title_fullStr Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title_full_unstemmed Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title_short Imaging Mass Spectrometry in Papillary Thyroid Carcinoma for the Identification and Validation of Biomarker Proteins
title_sort imaging mass spectrometry in papillary thyroid carcinoma for the identification and validation of biomarker proteins
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101781/
https://www.ncbi.nlm.nih.gov/pubmed/25045225
http://dx.doi.org/10.3346/jkms.2014.29.7.934
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