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Subcellular and in-vivo Nano-Endoscopy
Analysis of individual cells at the subcellular level is important for understanding diseases and accelerating drug discovery. Nanoscale endoscopes allow minimally invasive probing of individual cell interiors. Several such instruments have been presented previously, but they are either too complex...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046067/ https://www.ncbi.nlm.nih.gov/pubmed/27694854 http://dx.doi.org/10.1038/srep34400 |
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author | Cheemalapati, Surya Venkatasekhar Winskas, John Wang, Hao Konnaiyan, Karthik Zhdanov, Arseny Roth, Alison Adapa, Swamy Rakesh Deonarine, Andrew Noble, Mark Das, Tuhin Gatenby, Robert Westerheide, Sandy D. Jiang, Rays H. Y. Pyayt, Anna |
author_facet | Cheemalapati, Surya Venkatasekhar Winskas, John Wang, Hao Konnaiyan, Karthik Zhdanov, Arseny Roth, Alison Adapa, Swamy Rakesh Deonarine, Andrew Noble, Mark Das, Tuhin Gatenby, Robert Westerheide, Sandy D. Jiang, Rays H. Y. Pyayt, Anna |
author_sort | Cheemalapati, Surya Venkatasekhar |
collection | PubMed |
description | Analysis of individual cells at the subcellular level is important for understanding diseases and accelerating drug discovery. Nanoscale endoscopes allow minimally invasive probing of individual cell interiors. Several such instruments have been presented previously, but they are either too complex to fabricate or require sophisticated external detectors because of low signal collection efficiency. Here we present a nanoendoscope that can locally excite fluorescence in labelled cell organelles and collect the emitted signal for spectral analysis. Finite Difference Time Domain (FDTD) simulations have shown that with an optimized nanoendoscope taper profile, the light emission and collection was localized within ~100 nm. This allows signal detection to be used for nano-photonic sensing of the proximity of fluorophores. Upon insertion into the individual organelles of living cells, the nanoendoscope was fabricated and resultant fluorescent signals collected. This included the signal collection from the nucleus of Acridine orange labelled human fibroblast cells, the nucleus of Hoechst stained live liver cells and the mitochondria of MitoTracker Red labelled MDA-MB-231 cells. The endoscope was also inserted into a live organism, the yellow fluorescent protein producing nematode Caenorhabditis elegans, and a fluorescent signal was collected. To our knowledge this is the first demonstration of in vivo, local fluorescence signal collection on the sub-organelle level. |
format | Online Article Text |
id | pubmed-5046067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50460672016-10-11 Subcellular and in-vivo Nano-Endoscopy Cheemalapati, Surya Venkatasekhar Winskas, John Wang, Hao Konnaiyan, Karthik Zhdanov, Arseny Roth, Alison Adapa, Swamy Rakesh Deonarine, Andrew Noble, Mark Das, Tuhin Gatenby, Robert Westerheide, Sandy D. Jiang, Rays H. Y. Pyayt, Anna Sci Rep Article Analysis of individual cells at the subcellular level is important for understanding diseases and accelerating drug discovery. Nanoscale endoscopes allow minimally invasive probing of individual cell interiors. Several such instruments have been presented previously, but they are either too complex to fabricate or require sophisticated external detectors because of low signal collection efficiency. Here we present a nanoendoscope that can locally excite fluorescence in labelled cell organelles and collect the emitted signal for spectral analysis. Finite Difference Time Domain (FDTD) simulations have shown that with an optimized nanoendoscope taper profile, the light emission and collection was localized within ~100 nm. This allows signal detection to be used for nano-photonic sensing of the proximity of fluorophores. Upon insertion into the individual organelles of living cells, the nanoendoscope was fabricated and resultant fluorescent signals collected. This included the signal collection from the nucleus of Acridine orange labelled human fibroblast cells, the nucleus of Hoechst stained live liver cells and the mitochondria of MitoTracker Red labelled MDA-MB-231 cells. The endoscope was also inserted into a live organism, the yellow fluorescent protein producing nematode Caenorhabditis elegans, and a fluorescent signal was collected. To our knowledge this is the first demonstration of in vivo, local fluorescence signal collection on the sub-organelle level. Nature Publishing Group 2016-10-03 /pmc/articles/PMC5046067/ /pubmed/27694854 http://dx.doi.org/10.1038/srep34400 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cheemalapati, Surya Venkatasekhar Winskas, John Wang, Hao Konnaiyan, Karthik Zhdanov, Arseny Roth, Alison Adapa, Swamy Rakesh Deonarine, Andrew Noble, Mark Das, Tuhin Gatenby, Robert Westerheide, Sandy D. Jiang, Rays H. Y. Pyayt, Anna Subcellular and in-vivo Nano-Endoscopy |
title | Subcellular and in-vivo Nano-Endoscopy |
title_full | Subcellular and in-vivo Nano-Endoscopy |
title_fullStr | Subcellular and in-vivo Nano-Endoscopy |
title_full_unstemmed | Subcellular and in-vivo Nano-Endoscopy |
title_short | Subcellular and in-vivo Nano-Endoscopy |
title_sort | subcellular and in-vivo nano-endoscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046067/ https://www.ncbi.nlm.nih.gov/pubmed/27694854 http://dx.doi.org/10.1038/srep34400 |
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