Role of the N-terminus in permeability of chicken connexin45.6 gap junctional channels

被引:45
作者
Dong, Lixian
Liu, Xiaoqin
Li, Hui
Vertel, Barbara A.
Ebihara, Lisa
机构
[1] Rosalind Franklin Univ Med & Sci, Dept Physiol & Biophys, N Chicago, IL 60064 USA
[2] Rosalind Franklin Univ Med & Sci, Dept Cell Biol & Anat, N Chicago, IL 60064 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2006年 / 576卷 / 03期
关键词
D O I
10.1113/jphysiol.2006.113837
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have shown that gap junctional channels formed from the lens connexins Cx50 (or its chicken orthologue, Cx45.6) and Cx43 exhibit marked differences in transjunctional voltage gating and unitary conductance. In the present study, we used the negatively charged dye, Lucifer Yellow (LY), to examine and compare quantitative differences in dye transfer between pairs of HeLa cells stably transfected with Cx45.6 or Cx43. Our results show that Cx45.6 gap junctional channels are three times less permeable to LY than Cx43 channels. Replacement of the N-terminus of Cx45.6 with the corresponding domain of Cx43 increased LY permeability, reduced the transjunctional voltage (V-j) gating sensitivity, and reduced the unitary conductance of Cx45.6-43N gap junctional channels. Further experiments, using a series of Alexa probes that had similar net charge but varied in size showed that the Cx45.6-43N had a significantly higher permeability for the two largest Alexa dyes than Cx45.6. These data suggest that the N-terminus plays a critical role in determining many of biophysical properties of Cx45.6 gap junctional channels, including molecular permeability and voltage gating.
引用
收藏
页码:787 / 799
页数:13
相关论文
共 43 条
[1]   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
[2]  
BENNETT MVL, 1991, NEURON, V6, P305, DOI 10.1016/0896-6273(91)90241-Q
[3]   Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules [J].
Bevans, CG ;
Kordel, M ;
Rhee, SK ;
Harris, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :2808-2816
[4]   CONNEXIN43 - A PROTEIN FROM RAT-HEART HOMOLOGOUS TO A GAP JUNCTION PROTEIN FROM LIVER [J].
BEYER, EC ;
PAUL, DL ;
GOODENOUGH, DA .
JOURNAL OF CELL BIOLOGY, 1987, 105 (06) :2621-2629
[5]   A ring of eight conserved negatively charged amino acids doubles the conductance of BK channels and prevents inward rectification [J].
Brelidze, TI ;
Niu, XW ;
Magleby, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (15) :9017-9022
[6]  
Cao FL, 1998, J CELL SCI, V111, P31
[7]   SPECIFIC PERMEABILITY AND SELECTIVE FORMATION OF GAP JUNCTION CHANNELS IN CONNEXIN-TRANSFECTED HELA-CELLS [J].
ELFGANG, C ;
ECKERT, R ;
LICHTENBERGFRATE, H ;
BUTTERWECK, A ;
TRAUB, O ;
KLEIN, RA ;
HULSER, DF ;
WILLECKE, K .
JOURNAL OF CELL BIOLOGY, 1995, 129 (03) :805-817
[8]   FUNCTIONAL-ANALYSIS OF HUMAN CARDIAC GAP JUNCTION CHANNEL MUTANTS [J].
FISHMAN, GI ;
MORENO, AP ;
SPRAY, DC ;
LEINWAND, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3525-3529
[9]   Selective transfer of endogenous metabolites through gap junctions composed of different connexins [J].
Goldberg, GS ;
Lampe, PD ;
Nicholson, BJ .
NATURE CELL BIOLOGY, 1999, 1 (07) :457-459
[10]   Gap junctions between cells expressing connexin 43 or 32 show inverse permselectivity to adenosine and ATP [J].
Goldberg, GS ;
Moreno, AP ;
Lampe, PD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :36725-36730