Structure of the gap junction channel and its implications for its biological functions

被引:110
作者
Maeda, Shoji [1 ,2 ]
Tsukihara, Tomitake [1 ,2 ]
机构
[1] Osaka Univ, OLABB, Inst Prot Res, Suita, Osaka 5650874, Japan
[2] Univ Hyogo, Dept Life Sci, Akoh, Hyogo 6781297, Japan
关键词
Gap junction; Connexin; Electron microscopy; X-ray diffraction; Gating; Regulation; Permeability; Selectivity; DOMINANT CONGENITAL CATARACT; DIFFERENT CONNEXIN CHANNELS; EXTRACELLULAR LOOP DOMAIN; 3.5 ANGSTROM RESOLUTION; PORE-LINING RESIDUES; AMINO-ACID-RESIDUES; SELECTIVE PERMEABILITY; OCULODENTODIGITAL DYSPLASIA; 3-DIMENSIONAL STRUCTURE; INTERCELLULAR CHANNELS;
D O I
10.1007/s00018-010-0551-z
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
Gap junctions consist of arrays of intercellular channels composed of integral membrane proteins called connexin in vertebrates. Gap junction channels regulate the passage of ions and biological molecules between adjacent cells and, therefore, are critically important in many biological activities, including development, differentiation, neural activity, and immune response. Mutations in connexin genes are associated with several human diseases, such as neurodegenerative disease, skin disease, deafness, and developmental abnormalities. The activity of gap junction channels is regulated by the membrane voltage, intracellular microenvironment, interaction with other proteins, and phosphorylation. Each connexin channel has its own property for conductance and molecular permeability. A number of studies have tried to reveal the molecular architecture of the channel pore that should confer the connexin-specific permeability/selectivity properties and molecular basis for the gating and regulation. In this review, we give an overview of structural studies and describe the structural and functional relationship of gap junction channels.
引用
收藏
页码:1115 / 1129
页数:15
相关论文
共 181 条
[1]   Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice [J].
Ahmad, S ;
Chen, SP ;
Sun, JJ ;
Lin, X .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (02) :362-368
[2]  
Alberts B., 2008, Molecular biology of the cell, V5th, P1
[3]  
Alcoléa S, 1999, CIRC RES, V84, P1365
[4]   Four classes of intercellular channels between glial cells in the CNS [J].
Altevogt, BM ;
Paul, DL .
JOURNAL OF NEUROSCIENCE, 2004, 24 (18) :4313-4323
[5]   Heteromeric, but not homomeric, connexin channels are selectively permeable to inositol phosphates [J].
Ayad, Wafaa A. ;
Locke, Darren ;
Koreen, Irina V. ;
Harris, Andrew L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (24) :16727-16739
[6]   THE PROBABLE ARRANGEMENT OF THE HELICES IN G-PROTEIN-COUPLED RECEPTORS [J].
BALDWIN, JM .
EMBO JOURNAL, 1993, 12 (04) :1693-1703
[7]  
Bani-Yaghoub M, 1999, DEV GENET, V24, P69, DOI 10.1002/(SICI)1520-6408(1999)24:1/2<69::AID-DVG8>3.0.CO
[8]  
2-M
[9]   Functional expression in Xenopus Oocytes of gap-junctional hemichannels formed by a cysteine-less connexin 43 [J].
Bao, XY ;
Chen, YY ;
Reuss, L ;
Altenberg, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :9689-9692
[10]   Selective permeability of different connexin channels to the second messenger cyclic AMP [J].
Bedner, P ;
Niessen, H ;
Odermatt, B ;
Kretz, M ;
Willecke, K ;
Harz, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (10) :6673-6681