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Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging
Subcellular structures containing autophagy-related proteins of the Atg8 protein family have been investigated with conventional wide-field fluorescence and single molecule localisation microscopy. Fusion proteins of GABARAP and LC3B, respectively, with EYFP were overexpressed in HEK293 cells. While...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539863/ https://www.ncbi.nlm.nih.gov/pubmed/31086037 http://dx.doi.org/10.3390/molecules24091833 |
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author | Abdollahzadeh, Iman Hendriks, Johnny Sanwald, Julia L. Simons, Indra M. Hoffmann, Silke Weiergräber, Oliver H. Willbold, Dieter Gensch, Thomas |
author_facet | Abdollahzadeh, Iman Hendriks, Johnny Sanwald, Julia L. Simons, Indra M. Hoffmann, Silke Weiergräber, Oliver H. Willbold, Dieter Gensch, Thomas |
author_sort | Abdollahzadeh, Iman |
collection | PubMed |
description | Subcellular structures containing autophagy-related proteins of the Atg8 protein family have been investigated with conventional wide-field fluorescence and single molecule localisation microscopy. Fusion proteins of GABARAP and LC3B, respectively, with EYFP were overexpressed in HEK293 cells. While size distributions of structures labelled by the two proteins were found to be similar, shape distributions appeared quite disparate, with EYFP-GABARAP favouring circular structures and elliptical structures being dominant for EYFP-LC3B. The latter also featured a nearly doubled fraction of U-shape structures. The experimental results point towards highly differential localisation of the two proteins, which appear to label structures representing distinct stages or even specific channels of vesicular trafficking pathways. Our data also demonstrate that the application of super-resolution techniques expands the possibilities of fluorescence-based methods in autophagy studies and in some cases can rectify conclusions obtained from conventional fluorescence microscopy with diffraction-limited resolution. |
format | Online Article Text |
id | pubmed-6539863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65398632019-05-31 Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging Abdollahzadeh, Iman Hendriks, Johnny Sanwald, Julia L. Simons, Indra M. Hoffmann, Silke Weiergräber, Oliver H. Willbold, Dieter Gensch, Thomas Molecules Article Subcellular structures containing autophagy-related proteins of the Atg8 protein family have been investigated with conventional wide-field fluorescence and single molecule localisation microscopy. Fusion proteins of GABARAP and LC3B, respectively, with EYFP were overexpressed in HEK293 cells. While size distributions of structures labelled by the two proteins were found to be similar, shape distributions appeared quite disparate, with EYFP-GABARAP favouring circular structures and elliptical structures being dominant for EYFP-LC3B. The latter also featured a nearly doubled fraction of U-shape structures. The experimental results point towards highly differential localisation of the two proteins, which appear to label structures representing distinct stages or even specific channels of vesicular trafficking pathways. Our data also demonstrate that the application of super-resolution techniques expands the possibilities of fluorescence-based methods in autophagy studies and in some cases can rectify conclusions obtained from conventional fluorescence microscopy with diffraction-limited resolution. MDPI 2019-05-13 /pmc/articles/PMC6539863/ /pubmed/31086037 http://dx.doi.org/10.3390/molecules24091833 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Abdollahzadeh, Iman Hendriks, Johnny Sanwald, Julia L. Simons, Indra M. Hoffmann, Silke Weiergräber, Oliver H. Willbold, Dieter Gensch, Thomas Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title | Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title_full | Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title_fullStr | Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title_full_unstemmed | Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title_short | Autophagy-Related Proteins GABARAP and LC3B Label Structures of Similar Size but Different Shape in Super-Resolution Imaging |
title_sort | autophagy-related proteins gabarap and lc3b label structures of similar size but different shape in super-resolution imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539863/ https://www.ncbi.nlm.nih.gov/pubmed/31086037 http://dx.doi.org/10.3390/molecules24091833 |
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