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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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Autor principal: Lee, Clement M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2016
Materias:
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.
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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
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