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Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS
Altered cellular biomechanics have been implicated as key photogenic triggers in age-related diseases. An aberrant liquid-to-solid phase transition, observed in in vitro reconstituted droplets of FUS protein, has been recently proposed as a possible pathogenic mechanism for amyotrophic lateral scler...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131551/ https://www.ncbi.nlm.nih.gov/pubmed/30272018 http://dx.doi.org/10.1038/s42003-018-0148-x |
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author | Antonacci, Giuseppe de Turris, Valeria Rosa, Alessandro Ruocco, Giancarlo |
author_facet | Antonacci, Giuseppe de Turris, Valeria Rosa, Alessandro Ruocco, Giancarlo |
author_sort | Antonacci, Giuseppe |
collection | PubMed |
description | Altered cellular biomechanics have been implicated as key photogenic triggers in age-related diseases. An aberrant liquid-to-solid phase transition, observed in in vitro reconstituted droplets of FUS protein, has been recently proposed as a possible pathogenic mechanism for amyotrophic lateral sclerosis (ALS). Whether such transition occurs in cell environments is currently unknown as a consequence of the limited measuring capability of the existing techniques, which are invasive or lack of subcellular resolution. Here we developed a non-contact and label-free imaging method, named background-deflection Brillouin microscopy, to investigate the three-dimensional intracellular biomechanics at a sub-micron resolution. Our method exploits diffraction to achieve an unprecedented 10,000-fold enhancement in the spectral contrast of single-stage spectrometers, enabling, to the best of our knowledge, the first direct biomechanical analysis on intracellular stress granules containing ALS mutant FUS protein in fixed cells. Our findings provide fundamental insights on the critical aggregation step underlying the neurodegenerative ALS disease. |
format | Online Article Text |
id | pubmed-6131551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61315512018-09-28 Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS Antonacci, Giuseppe de Turris, Valeria Rosa, Alessandro Ruocco, Giancarlo Commun Biol Article Altered cellular biomechanics have been implicated as key photogenic triggers in age-related diseases. An aberrant liquid-to-solid phase transition, observed in in vitro reconstituted droplets of FUS protein, has been recently proposed as a possible pathogenic mechanism for amyotrophic lateral sclerosis (ALS). Whether such transition occurs in cell environments is currently unknown as a consequence of the limited measuring capability of the existing techniques, which are invasive or lack of subcellular resolution. Here we developed a non-contact and label-free imaging method, named background-deflection Brillouin microscopy, to investigate the three-dimensional intracellular biomechanics at a sub-micron resolution. Our method exploits diffraction to achieve an unprecedented 10,000-fold enhancement in the spectral contrast of single-stage spectrometers, enabling, to the best of our knowledge, the first direct biomechanical analysis on intracellular stress granules containing ALS mutant FUS protein in fixed cells. Our findings provide fundamental insights on the critical aggregation step underlying the neurodegenerative ALS disease. Nature Publishing Group UK 2018-09-10 /pmc/articles/PMC6131551/ /pubmed/30272018 http://dx.doi.org/10.1038/s42003-018-0148-x Text en © The Author(s) 2018 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 Antonacci, Giuseppe de Turris, Valeria Rosa, Alessandro Ruocco, Giancarlo Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title | Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title_full | Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title_fullStr | Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title_full_unstemmed | Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title_short | Background-deflection Brillouin microscopy reveals altered biomechanics of intracellular stress granules by ALS protein FUS |
title_sort | background-deflection brillouin microscopy reveals altered biomechanics of intracellular stress granules by als protein fus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131551/ https://www.ncbi.nlm.nih.gov/pubmed/30272018 http://dx.doi.org/10.1038/s42003-018-0148-x |
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