Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
The selectivity filter of the tandem pore potassium channel TASK-1 and its pH-sensitivity and ionic selectivity.
Yuill K
,
Ashmole I
,
Stanfield PR
.
???displayArticle.abstract???
We have studied pH sensitivity and ionic selectivity of the tandem pore K(+) channel TASK-1 heterologously expressed in Xenopus oocytes. We fit pH sensitivity assuming that only one of the two residues H98 need be protonated for channels to be shut. The effect of protons was weakly voltage dependent with a p K(a) of 6.02 at +40 mV. Replacement of His (H98D, H98N) reduced pH sensitivity but did not abolish it. Use of a concatameric channel permitted replacement of one His residue only; this concatamer was fully pH-sensitive. Increasing the number of His residues to 4 (mutant D204H) abolished pH sensitivity over the physiological range. The implication that D204 plays a role in pH-sensitivity was confirmed by the finding that pH sensitivity over the physiological range was also abolished in the mutant D204N. Ionic selectivity was also altered in D204H, D204N and H98D mutants. P(Rb)/ P(K) was increased from 0.80+/-0.04 (n=19) in wild type to 1.06+/-0.04 (n=19) in D204H. H98D, D204H and D204N were permeable to Na(+) with P(Na)/ P(K)=0.39+/-0.03 (n=14) in H98D, 0.64+/-0.04 (n=18) in D204H and 0.33+/-0.07 (n=3) in D204N. Thus, the arrangement of ring of residues HDHD appears to optimise both pH sensitivity and ionic selectivity.
Ashmole,
TASK-5, a novel member of the tandem pore K+ channel family.
2001, Pubmed,
Xenbase
Ashmole,
TASK-5, a novel member of the tandem pore K+ channel family.
2001,
Pubmed
,
Xenbase
Chapman,
GYGD pore motifs in neighbouring potassium channel subunits interact to determine ion selectivity.
2001,
Pubmed
Decher,
Characterization of TASK-4, a novel member of the pH-sensitive, two-pore domain potassium channel family.
2001,
Pubmed
,
Xenbase
Doyle,
The structure of the potassium channel: molecular basis of K+ conduction and selectivity.
1998,
Pubmed
Duprat,
TASK, a human background K+ channel to sense external pH variations near physiological pH.
1997,
Pubmed
,
Xenbase
Girard,
Genomic and functional characteristics of novel human pancreatic 2P domain K(+) channels.
2001,
Pubmed
,
Xenbase
Goldstein,
Potassium leak channels and the KCNK family of two-P-domain subunits.
2001,
Pubmed
Lesage,
Molecular and functional properties of two-pore-domain potassium channels.
2000,
Pubmed
Lesage,
Dimerization of TWIK-1 K+ channel subunits via a disulfide bridge.
1996,
Pubmed
,
Xenbase
Littleton,
Ion channels and synaptic organization: analysis of the Drosophila genome.
2000,
Pubmed
Lopes,
Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3.
2000,
Pubmed
,
Xenbase
Lopes,
Block of Kcnk3 by protons. Evidence that 2-P-domain potassium channel subunits function as homodimers.
2001,
Pubmed
,
Xenbase
Morton,
Determinants of pH sensing in the two-pore domain K(+) channels TASK-1 and -2.
2003,
Pubmed
,
Xenbase
Rajan,
TASK-3, a novel tandem pore domain acid-sensitive K+ channel. An extracellular histiding as pH sensor.
2000,
Pubmed
,
Xenbase
Rajan,
THIK-1 and THIK-2, a novel subfamily of tandem pore domain K+ channels.
2001,
Pubmed
,
Xenbase
Sano,
A novel two-pore domain K+ channel, TRESK, is localized in the spinal cord.
2003,
Pubmed
Silverman,
Asymmetrical contributions of subunit pore regions to ion selectivity in an inward rectifier K+ channel.
1998,
Pubmed
,
Xenbase
Thompson,
Residues beyond the selectivity filter of the K+ channel kir2.1 regulate permeation and block by external Rb+ and Cs+.
2000,
Pubmed
Wei,
Eight potassium channel families revealed by the C. elegans genome project.
1996,
Pubmed