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Intrinsic Disorder in the BK Channel and Its Interactome

The large-conductance Ca(2+)-activated K(+) (BK) channel is broadly expressed in various mammalian cells and tissues such as neurons, skeletal and smooth muscles, exocrine cells, and sensory cells of the inner ear. Previous studies suggest that BK channels are promiscuous binders involved in a multi...

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Autores principales: Peng, Zhenling, Sakai, Yoshihisa, Kurgan, Lukasz, Sokolowski, Bernd, Uversky, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984161/
https://www.ncbi.nlm.nih.gov/pubmed/24727949
http://dx.doi.org/10.1371/journal.pone.0094331
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author Peng, Zhenling
Sakai, Yoshihisa
Kurgan, Lukasz
Sokolowski, Bernd
Uversky, Vladimir
author_facet Peng, Zhenling
Sakai, Yoshihisa
Kurgan, Lukasz
Sokolowski, Bernd
Uversky, Vladimir
author_sort Peng, Zhenling
collection PubMed
description The large-conductance Ca(2+)-activated K(+) (BK) channel is broadly expressed in various mammalian cells and tissues such as neurons, skeletal and smooth muscles, exocrine cells, and sensory cells of the inner ear. Previous studies suggest that BK channels are promiscuous binders involved in a multitude of protein-protein interactions. To gain a better understanding of the potential mechanisms underlying BK interactions, we analyzed the abundance, distribution, and potential mechanisms of intrinsic disorder in 27 BK channel variants from mouse cochlea, 104 previously reported BK-associated proteins (BKAPS) from cytoplasmic and membrane/cytoskeletal regions, plus BK β- and γ-subunits. Disorder was evaluated using the MFDp algorithm, which is a consensus-based predictor that provides a strong and competitive predictive quality and PONDR, which can determine long intrinsically disordered regions (IDRs). Disorder-based binding sites or molecular recognition features (MoRFs) were found using MoRFpred and ANCHOR. BKAP functions were categorized based on Gene Ontology (GO) terms. The analyses revealed that the BK variants contain a number of IDRs. Intrinsic disorder is also common in BKAPs, of which ∼5% are completely disordered. However, intrinsic disorder is very differently distributed within BK and its partners. Approximately 65% of the disordered segments in BK channels are long (IDRs) (>50 residues), whereas >60% of the disordered segments in BKAPs are short IDRs that range in length from 4 to 30 residues. Both α and γ subunits showed various amounts of disorder as did hub proteins of the BK interactome. Our analyses suggest that intrinsic disorder is important for the function of BK and its BKAPs. Long IDRs in BK are engaged in protein-protein and protein-ligand interactions, contain multiple post-translational modification sites, and are subjected to alternative splicing. The disordered structure of BK and its BKAPs suggests one of the underlying mechanisms of their interaction.
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spelling pubmed-39841612014-04-15 Intrinsic Disorder in the BK Channel and Its Interactome Peng, Zhenling Sakai, Yoshihisa Kurgan, Lukasz Sokolowski, Bernd Uversky, Vladimir PLoS One Research Article The large-conductance Ca(2+)-activated K(+) (BK) channel is broadly expressed in various mammalian cells and tissues such as neurons, skeletal and smooth muscles, exocrine cells, and sensory cells of the inner ear. Previous studies suggest that BK channels are promiscuous binders involved in a multitude of protein-protein interactions. To gain a better understanding of the potential mechanisms underlying BK interactions, we analyzed the abundance, distribution, and potential mechanisms of intrinsic disorder in 27 BK channel variants from mouse cochlea, 104 previously reported BK-associated proteins (BKAPS) from cytoplasmic and membrane/cytoskeletal regions, plus BK β- and γ-subunits. Disorder was evaluated using the MFDp algorithm, which is a consensus-based predictor that provides a strong and competitive predictive quality and PONDR, which can determine long intrinsically disordered regions (IDRs). Disorder-based binding sites or molecular recognition features (MoRFs) were found using MoRFpred and ANCHOR. BKAP functions were categorized based on Gene Ontology (GO) terms. The analyses revealed that the BK variants contain a number of IDRs. Intrinsic disorder is also common in BKAPs, of which ∼5% are completely disordered. However, intrinsic disorder is very differently distributed within BK and its partners. Approximately 65% of the disordered segments in BK channels are long (IDRs) (>50 residues), whereas >60% of the disordered segments in BKAPs are short IDRs that range in length from 4 to 30 residues. Both α and γ subunits showed various amounts of disorder as did hub proteins of the BK interactome. Our analyses suggest that intrinsic disorder is important for the function of BK and its BKAPs. Long IDRs in BK are engaged in protein-protein and protein-ligand interactions, contain multiple post-translational modification sites, and are subjected to alternative splicing. The disordered structure of BK and its BKAPs suggests one of the underlying mechanisms of their interaction. Public Library of Science 2014-04-11 /pmc/articles/PMC3984161/ /pubmed/24727949 http://dx.doi.org/10.1371/journal.pone.0094331 Text en © 2014 Peng et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Peng, Zhenling
Sakai, Yoshihisa
Kurgan, Lukasz
Sokolowski, Bernd
Uversky, Vladimir
Intrinsic Disorder in the BK Channel and Its Interactome
title Intrinsic Disorder in the BK Channel and Its Interactome
title_full Intrinsic Disorder in the BK Channel and Its Interactome
title_fullStr Intrinsic Disorder in the BK Channel and Its Interactome
title_full_unstemmed Intrinsic Disorder in the BK Channel and Its Interactome
title_short Intrinsic Disorder in the BK Channel and Its Interactome
title_sort intrinsic disorder in the bk channel and its interactome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984161/
https://www.ncbi.nlm.nih.gov/pubmed/24727949
http://dx.doi.org/10.1371/journal.pone.0094331
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