Literature DB >> 20962011

Voltage-dependent block by internal spermine of the murine inwardly rectifying K+ channel, Kir2.1, with asymmetrical K+ concentrations.

Hiroko Matsuda1, Mikio Hayashi, Masayoshi Okada.   

Abstract

Effects of internal spermine on outward single-channel currents through a strongly inwardly rectifying K(+) channel (Kir2.1) were studied at asymmetrical K(+) concentrations (30 mm external and 150 mm internal K(+)). The current-voltage (I-V) relation for the single channel was almost linear and reversed at -37 ± 3 mV (V(R); n = 19). The channel conductance was 26.3 ± 1.3 pS (n = 24). The open-time and closed-time histograms were fitted with a single exponential function. Internal spermine at a concentration of 1-100 nm reduced the open time of the outward currents in a concentration-dependent manner and produced a blocked state. The steady-state open probability of the outward current decreased with larger depolarizations in both the absence and presence of internal spermine. The steady-state open probability with asymmetrical K(+) and symmetrical (150 mm external and internal K(+)) concentrations plotted against driving force (V - V(R)) coincided with smaller depolarizations in the absence of spermine and larger depolarizations and higher spermine concentrations in the presence of spermine. The blocking rate constants and unblock rates with 30 mm and 150 mm external K(+) were similar at the same driving force. The dissociation constant-membrane potential relation for 30 mm external K(+) was shifted in the negative direction from that for 150 mm external K(+) by 36 mV. These results suggested that the blocking kinetics depends on driving force to produce driving force-dependent inward rectification when the equilibrium potential for K(+) is altered by changing external K(+) and that the energy barriers and wells for blocking ions from passing or lodging are not stable but affected by external K(+) ions.

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Year:  2010        PMID: 20962011      PMCID: PMC3010137          DOI: 10.1113/jphysiol.2010.194480

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  31 in total

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5.  Voltage-dependent gating and block by internal spermine of the murine inwardly rectifying K+ channel, Kir2.1.

Authors:  Hiroko Matsuda; Keiko Oishi; Koichiro Omori
Journal:  J Physiol       Date:  2003-03-14       Impact factor: 5.182

6.  Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components.

Authors:  Lai-Hua Xie; Scott A John; James N Weiss
Journal:  J Physiol       Date:  2003-05-09       Impact factor: 5.182

7.  Potassium current and the effect of cesium on this current during anomalous rectification of the egg cell membrane of a starfish.

Authors:  S Hagiwara; S Miyazaki; N P Rosenthal
Journal:  J Gen Physiol       Date:  1976-06       Impact factor: 4.086

8.  Ionic blockage of sodium channels in nerve.

Authors:  A M Woodhull
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Authors:  Xiao Tao; Jose L Avalos; Jiayun Chen; Roderick MacKinnon
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10.  Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.

Authors:  C M Armstrong
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  4 in total

1.  The bundle crossing region is responsible for the inwardly rectifying internal spermine block of the Kir2.1 channel.

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2.  Waixenicin A inhibits cell proliferation through magnesium-dependent block of transient receptor potential melastatin 7 (TRPM7) channels.

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3.  A synergistic blocking effect of Mg²⁺ and spermine on the inward rectifier K⁺ (Kir2.1) channel pore.

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Journal:  Sci Rep       Date:  2016-02-12       Impact factor: 4.379

4.  Linkage analysis reveals allosteric coupling in Kir2.1 channels.

Authors:  Daniel M Sigg; Hsueh-Kai Chang; Ru-Chi Shieh
Journal:  J Gen Physiol       Date:  2018-10-16       Impact factor: 4.086

  4 in total

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