Voltage-gated proton channels: what's next?

被引:52
作者
DeCoursey, Thomas E. [1 ]
机构
[1] Rush Univ, Med Ctr, Dept Mol Biophys & Physiol, Chicago, IL 60612 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2008年 / 586卷 / 22期
关键词
D O I
10.1113/jphysiol.2008.161703
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This review is an attempt to identify and place in context some of the many questions about voltage-gated proton channels that remain unsolved. As the gene was identified only 2 years ago, the situation is very different than in fields where the gene has been known for decades. For the proton channel, most of the obvious and less obvious structure-function questions are still wide open. Remarkably, the proton channel protein strongly resembles the voltage-sensing domain of many voltage-gated ion channels, and thus offers a novel approach to study gating mechanisms. Another surprise is that the proton channel appears to function as a dimer, with two separate conduction pathways. A number of significant biological questions remain in dispute, unanswered, or in some cases, not yet asked. This latter deficit is ascribable to the intrinsic difficulty in evaluating the importance of one component in a complex system, and in addition, to the lack, until recently, of a means of performing an unambiguous lesion experiment, that is, of selectively eliminating the molecule in question. We still lack a potent, selective pharmacological inhibitor, but the identification of the gene has allowed the development of powerful new tools including proton channel antibodies, siRNA and knockout mice.
引用
收藏
页码:5305 / 5324
页数:20
相关论文
共 185 条
[1]   Contribution of the S4 segment to gating charge in the Shaker K+ channel [J].
Aggarwal, SK ;
MacKinnon, R .
NEURON, 1996, 16 (06) :1169-1177
[2]   PROTON CONDUCTANCE BY THE GRAMICIDIN WATER WIRE - MODEL FOR PROTON CONDUCTANCE IN THE F1F0 ATPASES [J].
AKESON, M ;
DEAMER, DW .
BIOPHYSICAL JOURNAL, 1991, 60 (01) :101-109
[3]  
Almers W, 1978, Rev Physiol Biochem Pharmacol, V82, P96, DOI 10.1007/BFb0030498
[4]   THE RESPIRATORY BURST OXIDASE AND THE MOLECULAR-BASIS OF CHRONIC GRANULOMATOUS-DISEASE [J].
BABIOR, BM .
AMERICAN JOURNAL OF HEMATOLOGY, 1991, 37 (04) :263-266
[5]   A novel H+ conductance in eosinophils:: Unique characteristics and absence in chronic granulomatous disease [J].
Bánfi, B ;
Schrenzel, J ;
Nüsse, O ;
Lew, DP ;
Ligeti, E ;
Krause, KH ;
Demaurex, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (02) :183-194
[6]   A mammalian H+ channel generated through alternative splicing of the NADPH oxidase homolog NOH-1 [J].
Bánfi, B ;
Maturana, A ;
Jaconi, S ;
Arnaudeau, S ;
Laforge, T ;
Sinha, B ;
Ligeti, E ;
Demaurex, N ;
Krause, KH .
SCIENCE, 2000, 287 (5450) :138-142
[7]   Regulation of eosinophil membrane depolarization during NADPH oxidase activation [J].
Bankers-Fulbright, JL ;
Gleich, GJ ;
Kephart, GM ;
Kita, H ;
O'Grady, SM .
JOURNAL OF CELL SCIENCE, 2003, 116 (15) :3221-3226
[8]   Regulation of human eosinophil NADPH oxidase activity:: A central role for PKCδ [J].
Bankers-Fulbright, JL ;
Kita, H ;
Gleich, GJ ;
O'Grady, SM .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 189 (03) :306-315
[9]   A VOLTAGE-GATED HYDROGEN-ION CURRENT IN THE OOCYTE MEMBRANE OF THE AXOLOTL, AMBYSTOMA [J].
BARISH, ME ;
BAUD, C .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 352 (JUL) :243-263
[10]   A VOLTAGE-DEPENDENT PROTON CURRENT IN CULTURED HUMAN SKELETAL-MUSCLE MYOTUBES [J].
BERNHEIM, L ;
KRAUSE, RM ;
BAROFFIO, A ;
HAMANN, M ;
KAELIN, A ;
BADER, CR .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 470 :313-333