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ThX – a next-generation probe for the early detection of amyloid aggregates
Neurodegenerative diseases such as Alzheimer's and Parkinson's are associated with protein misfolding and aggregation. Recent studies suggest that the small, rare and heterogeneous oligomeric species, formed early on in the aggregation process, may be a source of cytotoxicity. Thioflavin T...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159457/ https://www.ncbi.nlm.nih.gov/pubmed/34122915 http://dx.doi.org/10.1039/c9sc04730a |
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author | Needham, Lisa-Maria Weber, Judith Varela, Juan A. Fyfe, James W. B. Do, Dung T. Xu, Catherine K. Tutton, Luke Cliffe, Rachel Keenlyside, Benjamin Klenerman, David Dobson, Christopher M. Hunter, Christopher A. Müller, Karin H. O'Holleran, Kevin Bohndiek, Sarah E. Snaddon, Thomas N. Lee, Steven F. |
author_facet | Needham, Lisa-Maria Weber, Judith Varela, Juan A. Fyfe, James W. B. Do, Dung T. Xu, Catherine K. Tutton, Luke Cliffe, Rachel Keenlyside, Benjamin Klenerman, David Dobson, Christopher M. Hunter, Christopher A. Müller, Karin H. O'Holleran, Kevin Bohndiek, Sarah E. Snaddon, Thomas N. Lee, Steven F. |
author_sort | Needham, Lisa-Maria |
collection | PubMed |
description | Neurodegenerative diseases such as Alzheimer's and Parkinson's are associated with protein misfolding and aggregation. Recent studies suggest that the small, rare and heterogeneous oligomeric species, formed early on in the aggregation process, may be a source of cytotoxicity. Thioflavin T (ThT) is currently the gold-standard fluorescent probe for the study of amyloid proteins and aggregation processes. However, the poor photophysical and binding properties of ThT impairs the study of oligomers. To overcome this challenge, we have designed Thioflavin X, (ThX), a next-generation fluorescent probe which displays superior properties; including a 5-fold increase in brightness and 7-fold increase in binding affinity to amyloidogenic proteins. As an extrinsic dye, this can be used to study unique structural amyloid features both in bulk and on a single-aggregate level. Furthermore, ThX can be used as a super-resolution imaging probe in single-molecule localisation microscopy. Finally, the improved optical properties (extinction coefficient, quantum yield and brightness) of ThX can be used to monitor structural differences in oligomeric species, not observed via traditional ThT imaging. |
format | Online Article Text |
id | pubmed-8159457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81594572021-06-11 ThX – a next-generation probe for the early detection of amyloid aggregates Needham, Lisa-Maria Weber, Judith Varela, Juan A. Fyfe, James W. B. Do, Dung T. Xu, Catherine K. Tutton, Luke Cliffe, Rachel Keenlyside, Benjamin Klenerman, David Dobson, Christopher M. Hunter, Christopher A. Müller, Karin H. O'Holleran, Kevin Bohndiek, Sarah E. Snaddon, Thomas N. Lee, Steven F. Chem Sci Chemistry Neurodegenerative diseases such as Alzheimer's and Parkinson's are associated with protein misfolding and aggregation. Recent studies suggest that the small, rare and heterogeneous oligomeric species, formed early on in the aggregation process, may be a source of cytotoxicity. Thioflavin T (ThT) is currently the gold-standard fluorescent probe for the study of amyloid proteins and aggregation processes. However, the poor photophysical and binding properties of ThT impairs the study of oligomers. To overcome this challenge, we have designed Thioflavin X, (ThX), a next-generation fluorescent probe which displays superior properties; including a 5-fold increase in brightness and 7-fold increase in binding affinity to amyloidogenic proteins. As an extrinsic dye, this can be used to study unique structural amyloid features both in bulk and on a single-aggregate level. Furthermore, ThX can be used as a super-resolution imaging probe in single-molecule localisation microscopy. Finally, the improved optical properties (extinction coefficient, quantum yield and brightness) of ThX can be used to monitor structural differences in oligomeric species, not observed via traditional ThT imaging. The Royal Society of Chemistry 2020-02-21 /pmc/articles/PMC8159457/ /pubmed/34122915 http://dx.doi.org/10.1039/c9sc04730a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Needham, Lisa-Maria Weber, Judith Varela, Juan A. Fyfe, James W. B. Do, Dung T. Xu, Catherine K. Tutton, Luke Cliffe, Rachel Keenlyside, Benjamin Klenerman, David Dobson, Christopher M. Hunter, Christopher A. Müller, Karin H. O'Holleran, Kevin Bohndiek, Sarah E. Snaddon, Thomas N. Lee, Steven F. ThX – a next-generation probe for the early detection of amyloid aggregates |
title | ThX – a next-generation probe for the early detection of amyloid aggregates |
title_full | ThX – a next-generation probe for the early detection of amyloid aggregates |
title_fullStr | ThX – a next-generation probe for the early detection of amyloid aggregates |
title_full_unstemmed | ThX – a next-generation probe for the early detection of amyloid aggregates |
title_short | ThX – a next-generation probe for the early detection of amyloid aggregates |
title_sort | thx – a next-generation probe for the early detection of amyloid aggregates |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159457/ https://www.ncbi.nlm.nih.gov/pubmed/34122915 http://dx.doi.org/10.1039/c9sc04730a |
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