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Identification of Kinesin-1 Cargos Using Fluorescence Microscopy
Fluorescence microscopy is employed to identify Kinesin-1 cargos. Recently, the heavy chain of Kinesin-1 (KIF5B) was shown to transport the nuclear transcription factor c-MYC for proteosomal degradation in the cytoplasm. The method described here involves the study of a motorless KIF5B mutant for fl...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MyJove Corporation
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828159/ https://www.ncbi.nlm.nih.gov/pubmed/26966786 http://dx.doi.org/10.3791/53632 |
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author | Lee, Clement M. |
author_facet | Lee, Clement M. |
author_sort | Lee, Clement M. |
collection | PubMed |
description | Fluorescence microscopy is employed to identify Kinesin-1 cargos. Recently, the heavy chain of Kinesin-1 (KIF5B) was shown to transport the nuclear transcription factor c-MYC for proteosomal degradation in the cytoplasm. The method described here involves the study of a motorless KIF5B mutant for fluorescence microscopy. The wild-type and motorless KIF5B proteins are tagged with the fluorescent protein tdTomato. The wild-type tdTomato-KIF5B appears homogenously in the cytoplasm, while the motorless tdTomato-KIF5B mutant forms aggregates in the cytoplasm. Aggregation of the motorless KIF5B mutant induces aggregation of its cargo c-MYC in the cytoplasm. Hence, this method provides a visual means to identify the cargos of Kinesin-1. A similar strategy can be utilized to identify cargos of other motor proteins. |
format | Online Article Text |
id | pubmed-4828159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48281592016-04-22 Identification of Kinesin-1 Cargos Using Fluorescence Microscopy Lee, Clement M. J Vis Exp Biochemistry Fluorescence microscopy is employed to identify Kinesin-1 cargos. Recently, the heavy chain of Kinesin-1 (KIF5B) was shown to transport the nuclear transcription factor c-MYC for proteosomal degradation in the cytoplasm. The method described here involves the study of a motorless KIF5B mutant for fluorescence microscopy. The wild-type and motorless KIF5B proteins are tagged with the fluorescent protein tdTomato. The wild-type tdTomato-KIF5B appears homogenously in the cytoplasm, while the motorless tdTomato-KIF5B mutant forms aggregates in the cytoplasm. Aggregation of the motorless KIF5B mutant induces aggregation of its cargo c-MYC in the cytoplasm. Hence, this method provides a visual means to identify the cargos of Kinesin-1. A similar strategy can be utilized to identify cargos of other motor proteins. MyJove Corporation 2016-02-14 /pmc/articles/PMC4828159/ /pubmed/26966786 http://dx.doi.org/10.3791/53632 Text en Copyright © 2016, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Biochemistry Lee, Clement M. Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title | Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title_full | Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title_fullStr | Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title_full_unstemmed | Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title_short | Identification of Kinesin-1 Cargos Using Fluorescence Microscopy |
title_sort | identification of kinesin-1 cargos using fluorescence microscopy |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828159/ https://www.ncbi.nlm.nih.gov/pubmed/26966786 http://dx.doi.org/10.3791/53632 |
work_keys_str_mv | AT leeclementm identificationofkinesin1cargosusingfluorescencemicroscopy |