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Recombinant α-actin for specific fluorescent labeling

Until recently, actin was thought to act merely as a passive track for its motility partner, myosin, during actomyosin interactions. Yet a recent report having observed dynamical conformational changes in labeled skeletal muscle α-actin suggests that actin has a more active role. Because the labelin...

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Detalles Bibliográficos
Autores principales: Iwane, Atsuko H., Morimatsu, Masatoshi, Yanagida, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621554/
https://www.ncbi.nlm.nih.gov/pubmed/20009382
http://dx.doi.org/10.2183/pjab.85.491
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author Iwane, Atsuko H.
Morimatsu, Masatoshi
Yanagida, Toshio
author_facet Iwane, Atsuko H.
Morimatsu, Masatoshi
Yanagida, Toshio
author_sort Iwane, Atsuko H.
collection PubMed
description Until recently, actin was thought to act merely as a passive track for its motility partner, myosin, during actomyosin interactions. Yet a recent report having observed dynamical conformational changes in labeled skeletal muscle α-actin suggests that actin has a more active role. Because the labeling technique was still immature, however, conclusions regarding the significance of the different conformations are difficult to make. Here, we describe the preparation of fully active α-actin obtained from a baculovirus expression system. We developed α-actin recombinants, of which subdomains 1 and 2 have specific sites for fluorescent probes. This specific labeling technique offers to significantly expand the information acquired from actin studies.
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spelling pubmed-36215542013-05-02 Recombinant α-actin for specific fluorescent labeling Iwane, Atsuko H. Morimatsu, Masatoshi Yanagida, Toshio Proc Jpn Acad Ser B Phys Biol Sci Article Until recently, actin was thought to act merely as a passive track for its motility partner, myosin, during actomyosin interactions. Yet a recent report having observed dynamical conformational changes in labeled skeletal muscle α-actin suggests that actin has a more active role. Because the labeling technique was still immature, however, conclusions regarding the significance of the different conformations are difficult to make. Here, we describe the preparation of fully active α-actin obtained from a baculovirus expression system. We developed α-actin recombinants, of which subdomains 1 and 2 have specific sites for fluorescent probes. This specific labeling technique offers to significantly expand the information acquired from actin studies. The Japan Academy 2009-12 /pmc/articles/PMC3621554/ /pubmed/20009382 http://dx.doi.org/10.2183/pjab.85.491 Text en © 2009 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Iwane, Atsuko H.
Morimatsu, Masatoshi
Yanagida, Toshio
Recombinant α-actin for specific fluorescent labeling
title Recombinant α-actin for specific fluorescent labeling
title_full Recombinant α-actin for specific fluorescent labeling
title_fullStr Recombinant α-actin for specific fluorescent labeling
title_full_unstemmed Recombinant α-actin for specific fluorescent labeling
title_short Recombinant α-actin for specific fluorescent labeling
title_sort recombinant α-actin for specific fluorescent labeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621554/
https://www.ncbi.nlm.nih.gov/pubmed/20009382
http://dx.doi.org/10.2183/pjab.85.491
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AT morimatsumasatoshi recombinantaactinforspecificfluorescentlabeling
AT yanagidatoshio recombinantaactinforspecificfluorescentlabeling