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The IQ Motif is Crucial for Ca(v)1.1 Function
Ca(2+)-dependent modulation via calmodulin, with consensus CaM-binding IQ motif playing a key role, has been documented for most high-voltage-activated Ca(2+) channels. The skeletal muscle Ca(v)1.1 also exhibits Ca(2+)-/CaM-dependent modulation. Here, whole-cell Ca(2+) current, Ca(2+) transient, and...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228397/ https://www.ncbi.nlm.nih.gov/pubmed/22162637 http://dx.doi.org/10.1155/2011/504649 |
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author | Stroffekova, Katarina |
author_facet | Stroffekova, Katarina |
author_sort | Stroffekova, Katarina |
collection | PubMed |
description | Ca(2+)-dependent modulation via calmodulin, with consensus CaM-binding IQ motif playing a key role, has been documented for most high-voltage-activated Ca(2+) channels. The skeletal muscle Ca(v)1.1 also exhibits Ca(2+)-/CaM-dependent modulation. Here, whole-cell Ca(2+) current, Ca(2+) transient, and maximal, immobilization-resistant charge movement (Q(max)) recordings were obtained from cultured mouse myotubes, to test a role of IQ motif in function of Ca(v)1.1. The effect of introducing mutation (IQ to AA) of IQ motif into Ca(v)1.1 was examined. In dysgenic myotubes expressing YFP-Ca(v)1.1(AA), neither Ca(2+) currents nor evoked Ca(2+) transients were detectable. The loss of Ca(2+) current and excitation-contraction coupling did not appear to be a consequence of defective trafficking to the sarcolemma. The Q(max) in dysgenic myotubes expressing YFP-Ca(v)1.1(AA) was similar to that of normal myotubes. These findings suggest that the IQ motif of the Ca(v)1.1 may be an unrecognized site of structural and functional coupling between DHPR and RyR. |
format | Online Article Text |
id | pubmed-3228397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32283972011-12-08 The IQ Motif is Crucial for Ca(v)1.1 Function Stroffekova, Katarina J Biomed Biotechnol Research Article Ca(2+)-dependent modulation via calmodulin, with consensus CaM-binding IQ motif playing a key role, has been documented for most high-voltage-activated Ca(2+) channels. The skeletal muscle Ca(v)1.1 also exhibits Ca(2+)-/CaM-dependent modulation. Here, whole-cell Ca(2+) current, Ca(2+) transient, and maximal, immobilization-resistant charge movement (Q(max)) recordings were obtained from cultured mouse myotubes, to test a role of IQ motif in function of Ca(v)1.1. The effect of introducing mutation (IQ to AA) of IQ motif into Ca(v)1.1 was examined. In dysgenic myotubes expressing YFP-Ca(v)1.1(AA), neither Ca(2+) currents nor evoked Ca(2+) transients were detectable. The loss of Ca(2+) current and excitation-contraction coupling did not appear to be a consequence of defective trafficking to the sarcolemma. The Q(max) in dysgenic myotubes expressing YFP-Ca(v)1.1(AA) was similar to that of normal myotubes. These findings suggest that the IQ motif of the Ca(v)1.1 may be an unrecognized site of structural and functional coupling between DHPR and RyR. Hindawi Publishing Corporation 2011 2011-11-13 /pmc/articles/PMC3228397/ /pubmed/22162637 http://dx.doi.org/10.1155/2011/504649 Text en Copyright © 2011 Katarina Stroffekova. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Stroffekova, Katarina The IQ Motif is Crucial for Ca(v)1.1 Function |
title | The IQ Motif is Crucial for Ca(v)1.1 Function |
title_full | The IQ Motif is Crucial for Ca(v)1.1 Function |
title_fullStr | The IQ Motif is Crucial for Ca(v)1.1 Function |
title_full_unstemmed | The IQ Motif is Crucial for Ca(v)1.1 Function |
title_short | The IQ Motif is Crucial for Ca(v)1.1 Function |
title_sort | iq motif is crucial for ca(v)1.1 function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228397/ https://www.ncbi.nlm.nih.gov/pubmed/22162637 http://dx.doi.org/10.1155/2011/504649 |
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