Item Type: | Article |
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Title: | The C-terminal region of ahnak provides a link between cardiac L-type Ca2+ calcium channels and the actin-based cytoskeleton |
Creators Name: | Hohaus, A., Person, V., Behlke, J., Schaper, J., Morano, I. and Haase, H. |
Abstract: | Ahnak is a ubiquitously expressed giant protein of 5643 amino acids implicated in cell differentiation and signal transduction. In a recent study, we demonstrated the association of ahnak with the regulatory {beta}2 subunit of the cardiac L-type Ca2+ channel. Here we identify the most carboxyl-terminal ahnak region (aa 5262-5643) to interact with recombinant {beta}2a as well as with {beta}2 and {beta}1a isoforms of native muscle Ca2+ channels using a panel of GST fusion proteins. Equilibrium sedimentation analysis revealed Kd values of 55 ± 11 nM and 328 ± 24 nM for carboxyl-terminal (aa 195-606) and amino-terminal (aa 1-200) truncates of the {beta}2a subunit, respectively. The same carboxyl terminal ahnak region (aa 5262-5643) bound to G-actin and cosedimented with F-actin. Confocal microscopy of human left ventricular tissue localized the carboxyl terminal ahnak portion to the sarcolemma including the T-tubular system and the intercalated disks of cardiomyocytes. These results suggest that ahnak provides a structural basis for the subsarcolemmal cytoarchitecture and confers the regulatory role of the actin-based cytoskeleton to the L-type Ca2+ channel. |
Keywords: | {Beta}3 Subunit, Cardiomyocytes, L-Type Calcium Channel, Protein-Protein Interaction, Animals, Swine |
Source: | FASEB Journal |
ISSN: | 0892-6638 |
Publisher: | Federation of American Societies for Experimental Biology |
Volume: | 16 |
Number: | 10 |
Page Range: | 1205-1216 |
Date: | August 2002 |
Official Publication: | https://doi.org/10.1096/fj.01-0855com |
PubMed: | View item in PubMed |
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