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Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling

The Xin actin-binding repeat–containing proteins Xin and XIRP2 are exclusively expressed in striated muscle cells, where they are believed to play an important role in development. In adult muscle, both proteins are concentrated at attachment sites of myofibrils to the membrane. In contrast, during...

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Autores principales: Eulitz, Stefan, Sauer, Florian, Pelissier, Marie-Cecile, Boisguerin, Prisca, Molt, Sibylle, Schuld, Julia, Orfanos, Zacharias, Kley, Rudolf A., Volkmer, Rudolf, Wilmanns, Matthias, Kirfel, Gregor, van der Ven, Peter F. M., Fürst, Dieter O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810769/
https://www.ncbi.nlm.nih.gov/pubmed/23985323
http://dx.doi.org/10.1091/mbc.E13-04-0202
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author Eulitz, Stefan
Sauer, Florian
Pelissier, Marie-Cecile
Boisguerin, Prisca
Molt, Sibylle
Schuld, Julia
Orfanos, Zacharias
Kley, Rudolf A.
Volkmer, Rudolf
Wilmanns, Matthias
Kirfel, Gregor
van der Ven, Peter F. M.
Fürst, Dieter O.
author_facet Eulitz, Stefan
Sauer, Florian
Pelissier, Marie-Cecile
Boisguerin, Prisca
Molt, Sibylle
Schuld, Julia
Orfanos, Zacharias
Kley, Rudolf A.
Volkmer, Rudolf
Wilmanns, Matthias
Kirfel, Gregor
van der Ven, Peter F. M.
Fürst, Dieter O.
author_sort Eulitz, Stefan
collection PubMed
description The Xin actin-binding repeat–containing proteins Xin and XIRP2 are exclusively expressed in striated muscle cells, where they are believed to play an important role in development. In adult muscle, both proteins are concentrated at attachment sites of myofibrils to the membrane. In contrast, during development they are localized to immature myofibrils together with their binding partner, filamin C, indicating an involvement of both proteins in myofibril assembly. We identify the SH3 domains of nebulin and nebulette as novel ligands of proline-rich regions of Xin and XIRP2. Precise binding motifs are mapped and shown to bind both SH3 domains with micromolar affinity. Cocrystallization of the nebulette SH3 domain with the interacting XIRP2 peptide PPPTLPKPKLPKH reveals selective interactions that conform to class II SH3 domain–binding peptides. Bimolecular fluorescence complementation experiments in cultured muscle cells indicate a temporally restricted interaction of Xin-repeat proteins with nebulin/nebulette during early stages of myofibril development that is lost upon further maturation. In mature myofibrils, this interaction is limited to longitudinally oriented structures associated with myofibril development and remodeling. These data provide new insights into the role of Xin actin-binding repeat–containing proteins (together with their interaction partners) in myofibril assembly and after muscle damage.
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spelling pubmed-38107692013-12-30 Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling Eulitz, Stefan Sauer, Florian Pelissier, Marie-Cecile Boisguerin, Prisca Molt, Sibylle Schuld, Julia Orfanos, Zacharias Kley, Rudolf A. Volkmer, Rudolf Wilmanns, Matthias Kirfel, Gregor van der Ven, Peter F. M. Fürst, Dieter O. Mol Biol Cell Articles The Xin actin-binding repeat–containing proteins Xin and XIRP2 are exclusively expressed in striated muscle cells, where they are believed to play an important role in development. In adult muscle, both proteins are concentrated at attachment sites of myofibrils to the membrane. In contrast, during development they are localized to immature myofibrils together with their binding partner, filamin C, indicating an involvement of both proteins in myofibril assembly. We identify the SH3 domains of nebulin and nebulette as novel ligands of proline-rich regions of Xin and XIRP2. Precise binding motifs are mapped and shown to bind both SH3 domains with micromolar affinity. Cocrystallization of the nebulette SH3 domain with the interacting XIRP2 peptide PPPTLPKPKLPKH reveals selective interactions that conform to class II SH3 domain–binding peptides. Bimolecular fluorescence complementation experiments in cultured muscle cells indicate a temporally restricted interaction of Xin-repeat proteins with nebulin/nebulette during early stages of myofibril development that is lost upon further maturation. In mature myofibrils, this interaction is limited to longitudinally oriented structures associated with myofibril development and remodeling. These data provide new insights into the role of Xin actin-binding repeat–containing proteins (together with their interaction partners) in myofibril assembly and after muscle damage. The American Society for Cell Biology 2013-10-15 /pmc/articles/PMC3810769/ /pubmed/23985323 http://dx.doi.org/10.1091/mbc.E13-04-0202 Text en © 2013 Eulitz et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Eulitz, Stefan
Sauer, Florian
Pelissier, Marie-Cecile
Boisguerin, Prisca
Molt, Sibylle
Schuld, Julia
Orfanos, Zacharias
Kley, Rudolf A.
Volkmer, Rudolf
Wilmanns, Matthias
Kirfel, Gregor
van der Ven, Peter F. M.
Fürst, Dieter O.
Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title_full Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title_fullStr Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title_full_unstemmed Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title_short Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
title_sort identification of xin-repeat proteins as novel ligands of the sh3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810769/
https://www.ncbi.nlm.nih.gov/pubmed/23985323
http://dx.doi.org/10.1091/mbc.E13-04-0202
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