Visualization of the domain structure of an L-type Ca2+ channel using electron cryo-microscopy

被引:91
作者
Wolf, M
Eberhart, A
Glossmann, H
Striessnig, J
Grigorieff, N
机构
[1] Brandeis Univ, Rosenstiel Ctr, Howard Hughes Med Inst, Waltham, MA 02454 USA
[2] Inst Biochem Pharmacol, A-6020 Innsbruck, Austria
关键词
voltage-gated calcium channel subunits; immuno labeling; single-particle image processing; tetrad; excitation-contraction coupling complex;
D O I
10.1016/S0022-2836(03)00899-4
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
The three-dimensional structure of the skeletal muscle voltage-gated L-type calcium charnel (Ca(v)1.1; dihydropyridine receptor, DHPR) was determined using electron cryo-microscopy and single-particle averaging. The structure shows a single channel complex with an approximate total molecular mass of 550 kDa, corresponding to the five known subunits of the DHPR, and bound detergent and lipid. Features visible in our structure together with antibody labeling of the beta and alpha(2) subunits allowed us to assign locations for four of the five subunits within the structure. The most striking feature of the structure is the extra-cellular alpha(2) subunit that protrudes from the membrane domain in close proximity to the alpha(2) subunit. The cytosolic beta subunit is located close to the membrane and adjacent to subunits alpha(1), gamma and delta. Our structure correlates well with the functional and biochemical data available for this channel and suggests a three-dimensional model for the excitation-contraction coupling complex consisting of DHPR tetrads and the calcium release channel. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:171 / 182
页数:12
相关论文
共 53 条
[1]   γ1 subunit interactions within the skeletal muscle L-type voltage-gated calcium channels [J].
Arikkath, J ;
Chen, CC ;
Ahern, C ;
Allamand, V ;
Flanagan, JD ;
Coronado, R ;
Gregg, RG ;
Campbell, KP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) :1212-1219
[2]   Phospholipid solubilization during detergent extraction of rhodopsin from photoreceptor disk membranes [J].
Aveldano, MI .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 324 (02) :331-343
[3]   The skeletal muscle Ca2+ release channel has an oxidoreductase-like domain [J].
Baker, ML ;
Serysheva, II ;
Sencer, S ;
Wu, YL ;
Ludtke, SJ ;
Jiang, W ;
Hamilton, SL ;
Chiu, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (19) :12155-12160
[4]   Involvement of the carboxy-terminus region of the dihydropyridine receptor β1a subunit in excitation-contraction coupling of skeletal muscle [J].
Beurg, M ;
Ahern, CA ;
Vallejo, P ;
Conklin, MW ;
Powers, PA ;
Gregg, RG ;
Coronado, R .
BIOPHYSICAL JOURNAL, 1999, 77 (06) :2953-2967
[5]   The I-II loop of the Ca2+ channel α1 subunit contains an endoplasmic reticulum retention signal antagonized by the β subunit [J].
Bichet, D ;
Cornet, V ;
Geib, S ;
Carlier, E ;
Volsen, S ;
Hoshi, T ;
Mori, Y ;
De Waard, M .
NEURON, 2000, 25 (01) :177-190
[6]   STRUCTURAL EVIDENCE FOR DIRECT INTERACTION BETWEEN THE MOLECULAR-COMPONENTS OF THE TRANSVERSE TUBULE SARCOPLASMIC-RETICULUM JUNCTION IN SKELETAL-MUSCLE [J].
BLOCK, BA ;
IMAGAWA, T ;
CAMPBELL, KP ;
FRANZINIARMSTRONG, C .
JOURNAL OF CELL BIOLOGY, 1988, 107 (06) :2587-2600
[7]   Structure and regulation of voltage-gated Ca2+ channels [J].
Catterall, WA .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 :521-555
[8]  
Cheng W, 2003, BIOPHYS J, V84, p109A
[9]  
DEJONGH KS, 1990, J BIOL CHEM, V265, P14738
[10]   CHARACTERIZATION OF THE 2 SIZE FORMS OF THE ALPHA-1 SUBUNIT OF SKELETAL-MUSCLE L-TYPE CALCIUM CHANNELS [J].
DEJONGH, KS ;
WARNER, C ;
COLVIN, AA ;
CATTERALL, WA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10778-10782