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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
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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. |
format | Online Article Text |
id | pubmed-3810769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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