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Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry()
The identification of amyloid-binding compounds is a crucial step in the development of imaging probes and therapeutics for the detection and cure of Alzheimer's disease. Unfortunately, the process typically lags during the translation from in vitro to in vivo studies due to the impenetrable na...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778261/ https://www.ncbi.nlm.nih.gov/pubmed/24179813 http://dx.doi.org/10.1016/j.nicl.2013.04.015 |
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author | McClure, Richard A. Chumbley, Chad W. Reyzer, Michelle L. Wilson, Kevin Caprioli, Richard M. Gore, John C. Pham, Wellington |
author_facet | McClure, Richard A. Chumbley, Chad W. Reyzer, Michelle L. Wilson, Kevin Caprioli, Richard M. Gore, John C. Pham, Wellington |
author_sort | McClure, Richard A. |
collection | PubMed |
description | The identification of amyloid-binding compounds is a crucial step in the development of imaging probes and therapeutics for the detection and cure of Alzheimer's disease. Unfortunately, the process typically lags during the translation from in vitro to in vivo studies due to the impenetrable nature of the blood brain barrier (BBB). Here, we integrate fluorescence assay with MALDI imaging mass spectrometry to screen known compounds and repurpose their properties to enable the second function of binding to amyloid plaques. Through this approach, we identified an antihistamine compound, promethazine, that can bind to amyloid plaques. Finally, we demonstrate that promethazine is retained in the amyloid-burdened brain compared to a normal brain and that its distribution within the brain corroborates with that of amyloid plaques. |
format | Online Article Text |
id | pubmed-3778261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37782612013-10-31 Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() McClure, Richard A. Chumbley, Chad W. Reyzer, Michelle L. Wilson, Kevin Caprioli, Richard M. Gore, John C. Pham, Wellington Neuroimage Clin Article The identification of amyloid-binding compounds is a crucial step in the development of imaging probes and therapeutics for the detection and cure of Alzheimer's disease. Unfortunately, the process typically lags during the translation from in vitro to in vivo studies due to the impenetrable nature of the blood brain barrier (BBB). Here, we integrate fluorescence assay with MALDI imaging mass spectrometry to screen known compounds and repurpose their properties to enable the second function of binding to amyloid plaques. Through this approach, we identified an antihistamine compound, promethazine, that can bind to amyloid plaques. Finally, we demonstrate that promethazine is retained in the amyloid-burdened brain compared to a normal brain and that its distribution within the brain corroborates with that of amyloid plaques. Elsevier 2013-04-30 /pmc/articles/PMC3778261/ /pubmed/24179813 http://dx.doi.org/10.1016/j.nicl.2013.04.015 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article McClure, Richard A. Chumbley, Chad W. Reyzer, Michelle L. Wilson, Kevin Caprioli, Richard M. Gore, John C. Pham, Wellington Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title | Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title_full | Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title_fullStr | Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title_full_unstemmed | Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title_short | Identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and MALDI imaging mass spectrometry() |
title_sort | identification of promethazine as an amyloid-binding molecule using a fluorescence high-throughput assay and maldi imaging mass spectrometry() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778261/ https://www.ncbi.nlm.nih.gov/pubmed/24179813 http://dx.doi.org/10.1016/j.nicl.2013.04.015 |
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