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Resolving bundled microtubules using anti-tubulin nanobodies
Microtubules are hollow biopolymers of 25-nm diameter and are key constituents of the cytoskeleton. In neurons, microtubules are organized differently between axons and dendrites, but their precise organization in different compartments is not completely understood. Super-resolution microscopy techn...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918323/ https://www.ncbi.nlm.nih.gov/pubmed/26260773 http://dx.doi.org/10.1038/ncomms8933 |
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author | Mikhaylova, Marina Cloin, Bas M. C. Finan, Kieran van den Berg, Robert Teeuw, Jalmar Kijanka, Marta M. Sokolowski, Mikolaj Katrukha, Eugene A. Maidorn, Manuel Opazo, Felipe Moutel, Sandrine Vantard, Marylin Perez, Frank van Bergen en Henegouwen, Paul M. P. Hoogenraad, Casper C. Ewers, Helge Kapitein, Lukas C |
author_facet | Mikhaylova, Marina Cloin, Bas M. C. Finan, Kieran van den Berg, Robert Teeuw, Jalmar Kijanka, Marta M. Sokolowski, Mikolaj Katrukha, Eugene A. Maidorn, Manuel Opazo, Felipe Moutel, Sandrine Vantard, Marylin Perez, Frank van Bergen en Henegouwen, Paul M. P. Hoogenraad, Casper C. Ewers, Helge Kapitein, Lukas C |
author_sort | Mikhaylova, Marina |
collection | PubMed |
description | Microtubules are hollow biopolymers of 25-nm diameter and are key constituents of the cytoskeleton. In neurons, microtubules are organized differently between axons and dendrites, but their precise organization in different compartments is not completely understood. Super-resolution microscopy techniques can detect specific structures at an increased resolution, but the narrow spacing between neuronal microtubules poses challenges because most existing labelling strategies increase the effective microtubule diameter by 20–40 nm and will thereby blend neighbouring microtubules into one structure. Here we develop single-chain antibody fragments (nanobodies) against tubulin to achieve super-resolution imaging of microtubules with a decreased apparent diameter. To test the resolving power of these novel probes, we generate microtubule bundles with a known spacing of 50–70 nm and successfully resolve individual microtubules. Individual bundled microtubules can also be resolved in different mammalian cells, including hippocampal neurons, allowing novel insights into fundamental mechanisms of microtubule organization in cell- and neurobiology. |
format | Online Article Text |
id | pubmed-4918323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49183232016-07-07 Resolving bundled microtubules using anti-tubulin nanobodies Mikhaylova, Marina Cloin, Bas M. C. Finan, Kieran van den Berg, Robert Teeuw, Jalmar Kijanka, Marta M. Sokolowski, Mikolaj Katrukha, Eugene A. Maidorn, Manuel Opazo, Felipe Moutel, Sandrine Vantard, Marylin Perez, Frank van Bergen en Henegouwen, Paul M. P. Hoogenraad, Casper C. Ewers, Helge Kapitein, Lukas C Nat Commun Article Microtubules are hollow biopolymers of 25-nm diameter and are key constituents of the cytoskeleton. In neurons, microtubules are organized differently between axons and dendrites, but their precise organization in different compartments is not completely understood. Super-resolution microscopy techniques can detect specific structures at an increased resolution, but the narrow spacing between neuronal microtubules poses challenges because most existing labelling strategies increase the effective microtubule diameter by 20–40 nm and will thereby blend neighbouring microtubules into one structure. Here we develop single-chain antibody fragments (nanobodies) against tubulin to achieve super-resolution imaging of microtubules with a decreased apparent diameter. To test the resolving power of these novel probes, we generate microtubule bundles with a known spacing of 50–70 nm and successfully resolve individual microtubules. Individual bundled microtubules can also be resolved in different mammalian cells, including hippocampal neurons, allowing novel insights into fundamental mechanisms of microtubule organization in cell- and neurobiology. Nature Publishing Group 2015-08-11 /pmc/articles/PMC4918323/ /pubmed/26260773 http://dx.doi.org/10.1038/ncomms8933 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Mikhaylova, Marina Cloin, Bas M. C. Finan, Kieran van den Berg, Robert Teeuw, Jalmar Kijanka, Marta M. Sokolowski, Mikolaj Katrukha, Eugene A. Maidorn, Manuel Opazo, Felipe Moutel, Sandrine Vantard, Marylin Perez, Frank van Bergen en Henegouwen, Paul M. P. Hoogenraad, Casper C. Ewers, Helge Kapitein, Lukas C Resolving bundled microtubules using anti-tubulin nanobodies |
title | Resolving bundled microtubules using anti-tubulin nanobodies |
title_full | Resolving bundled microtubules using anti-tubulin nanobodies |
title_fullStr | Resolving bundled microtubules using anti-tubulin nanobodies |
title_full_unstemmed | Resolving bundled microtubules using anti-tubulin nanobodies |
title_short | Resolving bundled microtubules using anti-tubulin nanobodies |
title_sort | resolving bundled microtubules using anti-tubulin nanobodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918323/ https://www.ncbi.nlm.nih.gov/pubmed/26260773 http://dx.doi.org/10.1038/ncomms8933 |
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