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α-Synuclein–Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein Aggregation
[Image: see text] α-Synuclein fibrils are considered a hallmark of Parkinson’s disease and other synucleinopathies. However, small oligomers that formed during the early stages of α-synuclein aggregation are thought to be the main toxic species causing disease. The formation of α-synuclein oligomers...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534341/ https://www.ncbi.nlm.nih.gov/pubmed/30964656 http://dx.doi.org/10.1021/acs.analchem.8b03842 |
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author | Pérez-Pi, Irene Evans, David A. Horrocks, Mathew H. Pham, Nhan T. Dolt, Karamjit S. Koszela, Joanna Kunath, Tilo Auer, Manfred |
author_facet | Pérez-Pi, Irene Evans, David A. Horrocks, Mathew H. Pham, Nhan T. Dolt, Karamjit S. Koszela, Joanna Kunath, Tilo Auer, Manfred |
author_sort | Pérez-Pi, Irene |
collection | PubMed |
description | [Image: see text] α-Synuclein fibrils are considered a hallmark of Parkinson’s disease and other synucleinopathies. However, small oligomers that formed during the early stages of α-synuclein aggregation are thought to be the main toxic species causing disease. The formation of α-synuclein oligomers has proven difficult to follow, because of the heterogeneity and transient nature of the species formed. Here, a novel bead-based aggregation assay for monitoring the earliest stages of α-synuclein oligomerization, α-Synuclein–Confocal Nanoscanning (ASYN-CONA), is presented. The α-synuclein A91C single cysteine mutant is modified with a trifunctional chemical tag, which allows simultaneous fluorescent labeling with a green dye (tetramethylrhodamine, TMR) and attachment to microbeads. Beads with bound TMR-labeled α-synuclein are then incubated with a red dye (Cy5)-labeled variant of α-synuclein A91C, and EtOH (20%) to induce aggregation. Aggregation is detected by confocal scanning imaging, below the equatorial plane of the beads, which is known as the CONA technique. On-bead TMR-labeled α-synuclein and aggregated Cy5-labeled α-synuclein from the solution are quantitatively monitored in parallel by detection of fluorescent halos or “rings”. α-Synuclein on-bead oligomerization results in a linear increase of red bead ring fluorescence intensity over a period of 5 h. Total internal reflection fluorescence microscopy was performed on oligomers cleaved from the beads, and it revealed that (i) oligomers are sufficiently stable in solution to investigate their composition, consisting of 6 ± 1 monomer units, and (ii) oligomers containing a mean of 15 monomers bind Thioflavin-T. Various known inhibitors of α-synuclein aggregation were used to validate the ASYN-CONA assay for drug screening. Baicalein, curcumin, and rifampicin showed concentration-dependent inhibition of the α-synuclein aggregation and the IC(50) (the concentration of the compound at which the maxiumum intensity was reduced by one-half) were calculated. |
format | Online Article Text |
id | pubmed-6534341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65343412019-05-28 α-Synuclein–Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein Aggregation Pérez-Pi, Irene Evans, David A. Horrocks, Mathew H. Pham, Nhan T. Dolt, Karamjit S. Koszela, Joanna Kunath, Tilo Auer, Manfred Anal Chem [Image: see text] α-Synuclein fibrils are considered a hallmark of Parkinson’s disease and other synucleinopathies. However, small oligomers that formed during the early stages of α-synuclein aggregation are thought to be the main toxic species causing disease. The formation of α-synuclein oligomers has proven difficult to follow, because of the heterogeneity and transient nature of the species formed. Here, a novel bead-based aggregation assay for monitoring the earliest stages of α-synuclein oligomerization, α-Synuclein–Confocal Nanoscanning (ASYN-CONA), is presented. The α-synuclein A91C single cysteine mutant is modified with a trifunctional chemical tag, which allows simultaneous fluorescent labeling with a green dye (tetramethylrhodamine, TMR) and attachment to microbeads. Beads with bound TMR-labeled α-synuclein are then incubated with a red dye (Cy5)-labeled variant of α-synuclein A91C, and EtOH (20%) to induce aggregation. Aggregation is detected by confocal scanning imaging, below the equatorial plane of the beads, which is known as the CONA technique. On-bead TMR-labeled α-synuclein and aggregated Cy5-labeled α-synuclein from the solution are quantitatively monitored in parallel by detection of fluorescent halos or “rings”. α-Synuclein on-bead oligomerization results in a linear increase of red bead ring fluorescence intensity over a period of 5 h. Total internal reflection fluorescence microscopy was performed on oligomers cleaved from the beads, and it revealed that (i) oligomers are sufficiently stable in solution to investigate their composition, consisting of 6 ± 1 monomer units, and (ii) oligomers containing a mean of 15 monomers bind Thioflavin-T. Various known inhibitors of α-synuclein aggregation were used to validate the ASYN-CONA assay for drug screening. Baicalein, curcumin, and rifampicin showed concentration-dependent inhibition of the α-synuclein aggregation and the IC(50) (the concentration of the compound at which the maxiumum intensity was reduced by one-half) were calculated. American Chemical Society 2019-04-09 2019-05-07 /pmc/articles/PMC6534341/ /pubmed/30964656 http://dx.doi.org/10.1021/acs.analchem.8b03842 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Pérez-Pi, Irene Evans, David A. Horrocks, Mathew H. Pham, Nhan T. Dolt, Karamjit S. Koszela, Joanna Kunath, Tilo Auer, Manfred α-Synuclein–Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein Aggregation |
title | α-Synuclein–Confocal Nanoscanning
(ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein
Aggregation |
title_full | α-Synuclein–Confocal Nanoscanning
(ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein
Aggregation |
title_fullStr | α-Synuclein–Confocal Nanoscanning
(ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein
Aggregation |
title_full_unstemmed | α-Synuclein–Confocal Nanoscanning
(ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein
Aggregation |
title_short | α-Synuclein–Confocal Nanoscanning
(ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage α-Synuclein
Aggregation |
title_sort | α-synuclein–confocal nanoscanning
(asyn-cona), a bead-based assay for detecting early-stage α-synuclein
aggregation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534341/ https://www.ncbi.nlm.nih.gov/pubmed/30964656 http://dx.doi.org/10.1021/acs.analchem.8b03842 |
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