Labelling of the 3D structure of the cardiac L-type voltage-gated calcium channel

被引:9
作者
Walsh, Conor P. [1 ]
Davies, Anthony [2 ]
Nieto-Rostro, Manuela [2 ]
Dolphin, Annette C. [2 ]
Kitmitto, Ashraf [1 ]
机构
[1] Univ Manchester, Fac Med & Human Sci, Sch Clin & Lab Sci, Manchester, Lancs, England
[2] UCL, Dept Neurosci Physiol & Pharmacol, London, England
基金
英国惠康基金;
关键词
voltage-gated calcium channels; calmodulin; alpha2delta; Von Willebrand A domain; electron microscopy; CALMODULIN-BINDING; BETA-SUBUNIT; CRYSTAL-STRUCTURE; INACTIVATION; DOMAIN; COMPLEX; TRAFFICKING; MODULATION; HEART;
D O I
10.4161/chan.3.6.10225
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Voltage-gated calcium channels (VGCCs) regulate calcium influx into all excitable cells. In the heart, the main calcium channels are the L-type VGCCs (LTCCs). These are localised to the sarcolemmal membrane, and are hetero-oligomeric complexes comprised of three non-covalently associated polypeptides; alpha 1 (Ca(V)1.2), alpha(2)delta and beta. We recently reported the 3D structure for a monomeric form of the cardiac LTCC1 using electron microscopy and single particle analysis. We also determined the first medium/low resolution structure of a T-type voltage gated calcium channel (Ca(V)3.1) polypeptide. We identified the transmembrane and cytoplasmic domains of the T-type channel using labelling studies to determine the position of the C-terminus. By modelling of the Ca(V)3.1 structure (comparable at these resolutions to Ca(V)1.2) into the cardiac LTCC volume, we were able to delineate the subunit boundaries of the cardiac LTCC, leading to a proposal for a putative orientation of the LTCC with respect to the membrane bilayer. We have now extended these studies to include labelling of the extracellular alpha(2) polypeptide using affinity purified antibodies raised against the Von Willebrand Factor A (VWA) domain and calmodulin-gold labelling of the C-terminus of Ca(V)1.2. These data provide further support for the proposed orientation of the 3D structure of the cardiac LTCC.
引用
收藏
页码:387 / 392
页数:6
相关论文
共 28 条
[1]   Auxiliary subunits: essential components of the voltage-gated calcium channel complex [J].
Arikkath, J ;
Campbell, KP .
CURRENT OPINION IN NEUROBIOLOGY, 2003, 13 (03) :298-307
[2]   The L-type calcium channel in the heart: the beat goes on [J].
Bodi, I ;
Mikala, G ;
Koch, SE ;
Akhter, SA ;
Schwartz, A .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (12) :3306-3317
[3]   The metal-ion-dependent adhesion site in the Von Willebrand factor-A domain of α2δ subunits is key to trafficking voltage-gated Ca2+ channels [J].
Cantí, C ;
Nieto-Rostro, M ;
Foucault, I ;
Heblich, F ;
Wratten, J ;
Richards, MW ;
Hendrich, J ;
Douglas, L ;
Page, KM ;
Davies, A ;
Dolphin, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (32) :11230-11235
[4]   Functional biology of the α2δ subunits of voltage-gated calcium channels [J].
Davies, Anthony ;
Hendrich, Jan ;
Van Minh, Alexandra Tran ;
Wratten, Jack ;
Douglas, Leon ;
Dolphin, Annette C. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (05) :220-228
[5]   Crystal structure of dimeric cardiac L-type calcium channel regulatory domains bridged by Ca2+•calmodulins [J].
Fallon, Jennifer L. ;
Baker, Mariah R. ;
Xiong, Liangwen ;
Loy, Ryan E. ;
Yang, Guojun ;
Dirksen, Robert T. ;
Hamilton, Susan L. ;
Quiocho, Florante A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (13) :5135-5140
[6]   Structure of calmodulin bound to the hydrophobic IQ domain of the cardiac Cav1.2 calcium channel [J].
Fallon, JL ;
Halling, DB ;
Hamilton, SL ;
Quiocho, FA .
STRUCTURE, 2005, 13 (12) :1881-1886
[7]   SPIDER and WEB: Processing and visualization of images in 3D electron microscopy and related fields [J].
Frank, J ;
Radermacher, M ;
Penczek, P ;
Zhu, J ;
Li, YH ;
Ladjadj, M ;
Leith, A .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :190-199
[8]   Tissue-specific expression and gabapentin-binding properties of calcium channel α28 subunit subtypes [J].
Gong, HC ;
Hang, J ;
Kohler, W ;
Li, L ;
Su, TZ .
JOURNAL OF MEMBRANE BIOLOGY, 2001, 184 (01) :35-43
[9]   Cardiac L-type calcium channel β-subunits expressed in human heart have differential effects on single channel characteristics [J].
Hullin, R ;
Khan, IFY ;
Wirtz, S ;
Mohacsi, P ;
Varadi, G ;
Schwartz, A ;
Herzig, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21623-21630
[10]   Structures of CaV2Ca2+/CaM-IQ Domain Complexes Reveal Binding Modes that Underlie Calcium-Dependent Inactivation and Facilitation [J].
Kim, Eun Young ;
Rumpf, Christine H. ;
Fujiwara, Yuichiro ;
Cooley, Elizabeth S. ;
Van Petegem, Filip ;
Minor, Daniel L., Jr. .
STRUCTURE, 2008, 16 (10) :1455-1467