The Croonian Lecture 2000. Nicotinic acetylcholine receptor and the structural basis of fast synaptic transmission

被引:99
作者
Unwin, N [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
关键词
acetylcholine receptor; gap junction; synapse; electron microscopy;
D O I
10.1098/rstb.2000.0737
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Communication in the nervous system takes place at chemical and electrical synapses, where neurotransmitter-gated ion channels, such as the nicotinic acetylcholine (ACh) receptor, and gap junction channels control propagation of electrical signals from one cell to the next. Newly developed electron crystallographic methods have revealed the structures of these channels trapped in open as well as closed states, suggesting how they work. The ACh receptor has large vestibules extending from the membrane which shape the ACh-binding pockets and facilitate selective transport of cations across a narrow membrane-spanning pore. When ACh enters the pockets it triggers a concerted conformational change that opens the pore by destabilizing a gate in the middle of the membrane made by a ring of pore-lining a-helical segments. The alternative 'open' configuration of pore-lining segments reshapes the lumen and creates new surfaces, allowing the ions to pass through. The gap junction channel uses a similar structural mechanism, involving coordinated rearrangements of alpha -helical segments in the plane of the membrane, to open its pore.
引用
收藏
页码:1813 / 1829
页数:17
相关论文
共 97 条
[1]   COMPUTATIONAL SEARCHING AND MUTAGENESIS SUGGEST A STRUCTURE FOR THE PENTAMERIC TRANSMEMBRANE DOMAIN OF PHOSPHOLAMBAN [J].
ADAMS, PD ;
ARKIN, IT ;
ENGELMAN, DM ;
BRUNGER, AT .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (02) :154-162
[2]   Electrostatics and the ion selectivity of ligand-gated channels [J].
Adcock, C ;
Smith, GR ;
Sansom, MSP .
BIOPHYSICAL JOURNAL, 1998, 75 (03) :1211-1222
[3]  
[Anonymous], BIOPHYSICAL ELECT MI
[4]   Seeing is relieving: electrical synapses between visualized neurons [J].
Bennett, MVL .
NATURE NEUROSCIENCE, 2000, 3 (01) :7-9
[5]   Distortion correction of tubular crystals: improvements in the acetylcholine receptor structure [J].
Beroukhim, R ;
Unwin, N .
ULTRAMICROSCOPY, 1997, 70 (1-2) :57-81
[6]   ANALYSIS OF TRANSIENT STRUCTURES BY CRYOMICROSCOPY COMBINED WITH RAPID MIXING OF SPRAY DROPLETS [J].
BERRIMAN, J ;
UNWIN, N .
ULTRAMICROSCOPY, 1994, 56 (04) :241-252
[7]   Probing the structure of the nicotinic acetylcholine receptor ion channel with the uncharged photoactivable compound [3H]diazofluorene [J].
Blanton, MP ;
Dangott, LJ ;
Raja, SK ;
Lala, AK ;
Cohen, JB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) :8659-8668
[8]   QUATERNARY STRUCTURE OF THE ACETYLCHOLINE-RECEPTOR [J].
BRISSON, A ;
UNWIN, PNT .
NATURE, 1985, 315 (6019) :474-477
[9]   TUBULAR CRYSTALS OF ACETYLCHOLINE-RECEPTOR [J].
BRISSON, A ;
UNWIN, PNT .
JOURNAL OF CELL BIOLOGY, 1984, 99 (04) :1202-1211
[10]   STEREOCHEMICAL STUDIES OF CYCLIC PEPTIDES .4. ENERGY CALCULATIONS OF CYCLIC DISULPHIDE CYSTEINYLCYSTEINE [J].
CHANDRAS.R ;
BALASUBR.R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 188 (01) :1-&