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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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