Literature DB >> 9876139

Contribution of the selectivity filter to inactivation in potassium channels.

L Kiss1, J LoTurco, S J Korn.   

Abstract

Voltage-gated K+ channels exhibit a slow inactivation process, which becomes an important influence on the rate of action potential repolarization during prolonged or repetitive depolarization. During slow inactivation, the outer mouth of the permeation pathway undergoes a conformational change. We report here that during the slow inactivation process, the channel progresses through at least three permeation states; from the initial open state that is highly selective for K+, the channel enters a state that is less permeable to K+ and more permeable to Na+, and then proceeds to a state that is non-conducting. Similar results were obtained in three different voltage-gated K+ channels: Kv2.1, a channel derived from Shaker (Shaker Delta A463C), and a chimeric channel derived from Kv2.1 and Kv1.3 that displays classical C-type inactivation. The change in selectivity displayed both voltage- and time-dependent properties of slow inactivation and was observed with K+ on either side of the channel. Elevation of internal [K+] inhibited Na+ conduction through the inactivating channel in a concentration-dependent manner. These results indicate that the change in selectivity filter function is an integral part of the slow inactivation mechanism, and argue against the hypothesis that the inactivation gate is independent from the selectivity filter. Thus, these data suggest that the selectivity filter is itself the inactivation gate.

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Year:  1999        PMID: 9876139      PMCID: PMC1302516          DOI: 10.1016/S0006-3495(99)77194-8

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  29 in total

1.  Recovery from C-type inactivation is modulated by extracellular potassium.

Authors:  D I Levy; C Deutsch
Journal:  Biophys J       Date:  1996-02       Impact factor: 4.033

2.  Permeation selectivity by competition in a delayed rectifier potassium channel.

Authors:  S J Korn; S R Ikeda
Journal:  Science       Date:  1995-07-21       Impact factor: 47.728

3.  Dynamic rearrangement of the outer mouth of a K+ channel during gating.

Authors:  Y Liu; M E Jurman; G Yellen
Journal:  Neuron       Date:  1996-04       Impact factor: 17.173

4.  Use-dependent blockers and exit rate of the last ion from the multi-ion pore of a K+ channel.

Authors:  T Baukrowitz; G Yellen
Journal:  Science       Date:  1996-02-02       Impact factor: 47.728

5.  Cooperative subunit interactions in C-type inactivation of K channels.

Authors:  E M Ogielska; W N Zagotta; T Hoshi; S H Heinemann; J Haab; R W Aldrich
Journal:  Biophys J       Date:  1995-12       Impact factor: 4.033

6.  C-type inactivation of a voltage-gated K+ channel occurs by a cooperative mechanism.

Authors:  G Panyi; Z Sheng; C Deutsch
Journal:  Biophys J       Date:  1995-09       Impact factor: 4.033

7.  Transfer of the scorpion toxin receptor to an insensitive potassium channel.

Authors:  A Gross; T Abramson; R MacKinnon
Journal:  Neuron       Date:  1994-10       Impact factor: 17.173

8.  State-dependent inactivation of the Kv3 potassium channel.

Authors:  S Marom; I B Levitan
Journal:  Biophys J       Date:  1994-08       Impact factor: 4.033

9.  Ion conduction through C-type inactivated Shaker channels.

Authors:  J G Starkus; L Kuschel; M D Rayner; S H Heinemann
Journal:  J Gen Physiol       Date:  1997-11       Impact factor: 4.086

10.  The interaction of Na+ and K+ in voltage-gated potassium channels. Evidence for cation binding sites of different affinity.

Authors:  L Kiss; D Immke; J LoTurco; S J Korn
Journal:  J Gen Physiol       Date:  1998-02       Impact factor: 4.086

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  97 in total

1.  A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation.

Authors:  Y Y Vilin; E Fujimoto; P C Ruben
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

2.  Structural determinants of slow inactivation in human cardiac and skeletal muscle sodium channels.

Authors:  Y Y Vilin; N Makita; A L George; P C Ruben
Journal:  Biophys J       Date:  1999-09       Impact factor: 4.033

3.  Molecular dynamics study of the KcsA potassium channel.

Authors:  T W Allen; S Kuyucak; S H Chung
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

4.  Potassium inhibition of sodium-activated potassium (K(Na)) channels in guinea-pig ventricular myocytes.

Authors:  X W Niu; R W Meech
Journal:  J Physiol       Date:  2000-07-01       Impact factor: 5.182

5.  Gating charge immobilization caused by the transition between inactivated states in the Kv1.5 channel.

Authors:  Z Wang; D Fedida
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

6.  Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel.

Authors:  J S Fan; M Jiang; W Dun; T V McDonald; G N Tseng
Journal:  Biophys J       Date:  1999-06       Impact factor: 4.033

7.  Relationship between pore occupancy and gating in BK potassium channels.

Authors:  Rebecca A Piskorowski; Richard W Aldrich
Journal:  J Gen Physiol       Date:  2006-05       Impact factor: 4.086

8.  Slow inactivation of the Ca(V)3.1 isotype of T-type calcium channels.

Authors:  Julien Hering; Anne Feltz; Régis C Lambert
Journal:  J Physiol       Date:  2003-12-23       Impact factor: 5.182

9.  C-type inactivation involves a significant decrease in the intracellular aqueous pore volume of Kv1.4 K+ channels expressed in Xenopus oocytes.

Authors:  XueJun Jiang; Glenna C L Bett; XiaoYan Li; Vladimir E Bondarenko; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

10.  Low-affinity Na+ uptake in the halophyte Suaeda maritima.

Authors:  Suo-Min Wang; Jin-Lin Zhang; Timothy J Flowers
Journal:  Plant Physiol       Date:  2007-08-31       Impact factor: 8.340

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