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Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid
One of the pathological hallmarks of Alzheimer’s disease (AD) is the abnormal aggregation of amyloid beta (Aβ) peptides. Therefore the detection of Aβ peptides and imaging of amyloid plaques are considered as promising diagnostic methods for AD. Here we report a bifunctional nanoprobe prepared by co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560097/ https://www.ncbi.nlm.nih.gov/pubmed/31186449 http://dx.doi.org/10.1038/s41598-019-43288-2 |
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author | Xia, Yang Padmanabhan, Parasuraman Sarangapani, Sreelatha Gulyás, Balázs Vadakke Matham, Murukeshan |
author_facet | Xia, Yang Padmanabhan, Parasuraman Sarangapani, Sreelatha Gulyás, Balázs Vadakke Matham, Murukeshan |
author_sort | Xia, Yang |
collection | PubMed |
description | One of the pathological hallmarks of Alzheimer’s disease (AD) is the abnormal aggregation of amyloid beta (Aβ) peptides. Therefore the detection of Aβ peptides and imaging of amyloid plaques are considered as promising diagnostic methods for AD. Here we report a bifunctional nanoprobe prepared by conjugating gold nanoparticles (AuNPs) with Rose Bengal (RB) dye. RB is chosen due to its unique Raman fingerprints and affinity with Aβ peptides. After the conjugation, Raman signals of RB were significantly enhanced due to the surface-enhanced Raman scattering (SERS) effect. Upon binding with Aβ42 peptides, a spectrum change was detected, and the magnitude of the spectrum changes can be correlated with the concentration of target peptides. The peptide/probe interaction also induced a remarkable enhancement in the probes’ fluorescence emission. This fluorescence enhancement was further utilized to image amyloid plaques in the brain slices from transgenic mice. In this study, the RB-AuNPs were used for both SERS-based detection of Aβ42 peptides and fluorescence-based imaging of amyloid plaques. Compared to monofunctional probes, the multifunctional probe is capable to provide more comprehensive pathophysiological information, and therefore, the implementation of such multifunctional amyloid probes is expected to help the investigation of amyloid aggregation and the early diagnosis of AD. |
format | Online Article Text |
id | pubmed-6560097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65600972019-06-19 Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid Xia, Yang Padmanabhan, Parasuraman Sarangapani, Sreelatha Gulyás, Balázs Vadakke Matham, Murukeshan Sci Rep Article One of the pathological hallmarks of Alzheimer’s disease (AD) is the abnormal aggregation of amyloid beta (Aβ) peptides. Therefore the detection of Aβ peptides and imaging of amyloid plaques are considered as promising diagnostic methods for AD. Here we report a bifunctional nanoprobe prepared by conjugating gold nanoparticles (AuNPs) with Rose Bengal (RB) dye. RB is chosen due to its unique Raman fingerprints and affinity with Aβ peptides. After the conjugation, Raman signals of RB were significantly enhanced due to the surface-enhanced Raman scattering (SERS) effect. Upon binding with Aβ42 peptides, a spectrum change was detected, and the magnitude of the spectrum changes can be correlated with the concentration of target peptides. The peptide/probe interaction also induced a remarkable enhancement in the probes’ fluorescence emission. This fluorescence enhancement was further utilized to image amyloid plaques in the brain slices from transgenic mice. In this study, the RB-AuNPs were used for both SERS-based detection of Aβ42 peptides and fluorescence-based imaging of amyloid plaques. Compared to monofunctional probes, the multifunctional probe is capable to provide more comprehensive pathophysiological information, and therefore, the implementation of such multifunctional amyloid probes is expected to help the investigation of amyloid aggregation and the early diagnosis of AD. Nature Publishing Group UK 2019-06-11 /pmc/articles/PMC6560097/ /pubmed/31186449 http://dx.doi.org/10.1038/s41598-019-43288-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xia, Yang Padmanabhan, Parasuraman Sarangapani, Sreelatha Gulyás, Balázs Vadakke Matham, Murukeshan Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title | Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title_full | Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title_fullStr | Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title_full_unstemmed | Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title_short | Bifunctional Fluorescent/Raman Nanoprobe for the Early Detection of Amyloid |
title_sort | bifunctional fluorescent/raman nanoprobe for the early detection of amyloid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560097/ https://www.ncbi.nlm.nih.gov/pubmed/31186449 http://dx.doi.org/10.1038/s41598-019-43288-2 |
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