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Research on inactivation of the hybrid K channel.

Research Project

Project/Area Number 07670099
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General pharmacology
Research InstitutionTohoku University

Principal Investigator

NUNOKI Kazuo  Tohoku Univ., Dept.of Pharmacol., Assit.Prof., 医学部, 講師 (10172743)

Co-Investigator(Kenkyū-buntansha) ISHII Kuniaki  Yamagata Univ., Dept.of Pharmacol., Assoc.Prof., 医学部, 助教授 (10184459)
Project Period (FY) 1995 – 1996
Project Status Completed (Fiscal Year 1996)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1995: ¥1,500,000 (Direct Cost: ¥1,500,000)
Keywordshybrid K channel / inactivation / tandem linkage / Kv1.4 / Kv1.2 / Xenopus oocyte / 電位依存性Kチャンネル / ハイブリッドチャンネル
Research Abstract

We previously reported that the current observed in Kv1.4/Kv1.2 hybrid channel is very similar to that of the homotetrameric Kv1.4 channel ; which shows rapid inactivation during depolarizing pulses. It has been elucidated that in the hybrid channel the S4-S5 intracellular loop of non-inactivating subunit Kv1.2 could be part of the acceptor for the inactivation gates thetered from Kv1.4 subunit. This project was planned in order to investigate the relative contribution of the constitutive subunits to inactivation of the currents. The effects of a point mutation in the S4-S5 loop of Kv1.4 or Kv1.2 on inactivation of the hybrid channel were examined. Mutations in the S4-S5 loop of Kv1.4 and the corresponding amino acid of Kv1.2 had similar effects on inactivation time constant, suggesting that all of the S4-S5 loops derived from each constituent subunit equally contribute to inactivation as the acceptor for the inactivation gates.
The role of the S5-S6 regions of Kv1.4 and Kv1.2 subunits in inactivation was also examined. The fusion genes encoding the hybrid channels were constructed, in which S5-S6 region of Kv1.4 or Kv1.2 was replaced with the corresponding region of Kv1.2 or Kv1.4, or the S5-S6 regions were interchanged between the two components. Characteristics of inactivation for all of these hybrid channels were similar. It was suggested from these results that the S5-S6 regions of all constituent subunits equally contribute to inactivation of the currents.

Report

(3 results)
  • 1996 Annual Research Report   Final Research Report Summary
  • 1995 Annual Research Report
  • Research Products

    (16 results)

All Other

All Publications (16 results)

  • [Publications] Kazuo Nunoki et al.: "Role of S5〜S6 regions of the subunits in inactivation of Kv1.4/Kv1.2 hybrid channel." Japan.J.Pharmacol.73suppl.I. 190 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Kazuo Nunoki et al.: "Contribution of subunits to inactivation of the hybrid K channel." Japan.J.Pharmacol.71suppl.I. 157 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yoshiteru Sasaki et al.: "Voltape-dependent R^+ channel (Rvl.5) cloned from rabbit heart and faulitation of inaotivation of the delayed rectifier current by βsubunit." FEBS Lett. 372. 20-24 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Hideyuki Murakoshi et al.: "Determination of K^A values by controlled receptor expression in Xenopus oocytes." Br.J.Pharmacol.116. 2062-2066 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Kazuo Nunoki, et al: "Role of S5-S6 regions of the subunits in inactivation Kv1.4/Kv1.2 hybrid channel" Japan.J.Pharmacol. 73 suppl.I. 190 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Kazuo Nunoki, et al: "Contribution of subunits to inactivaton of the hybrid K channel." Japan.J.Pharmacol. 71 suppl.I. 157 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yoshiteru Sasaki, et al.: "voltage-dependent K^+ channel (Kv1.5) cloned from rabbit heart and facilitation of inactivation of the delayd rectifier current by beta subunit." FEBS Lett. 372. 20-24 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Hideyuki Murakoshi, et al.: "Determination of K_A values by controlled receptor expression inXenopus oocytes." Br.J.Pharmacol.116. 2062-2066 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Kazuo Nunoki et al.: "Role of S5-S6 regions of the subunits in inactivation of Kv1.4/Kv1.2 hybrid channel." Japan. J. Pharmacol.73supplI. 190 (1997)

    • Related Report
      1996 Annual Research Report
  • [Publications] Kazuo Nunoki et al.: "Contribution of subunits to inactivation of the hybrid K channel." Japan. J. Pharmacol.71supplI. 157 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Yoshiteru Sasaki et al.: "Voltage-dependent K^+ channel (Kv1.5) cloned from rabbit heart and facilitation of inactivation of the delayed rectifier current by β subunit." FEBS Lett. 372. 20-24 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] Hideyuki Murakoshi et al.: "Determination of K_A values by controlled receptor expression in Xenopus oocytes." Br. J. Phamaclo.116. 2062-2066 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] Nunoki, K.: "Inactivation of the hybrid K channels" Japan. J. Pharmacol. Suppl. I. 67. 64p (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Murakoshi, H.: "Determination of K_A values by controlled receptor expression in Xenopus oocytes" Br. J. Pharmacol.116. 2062-2066 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Sasaki, Y.: "Voltage-dependent K^+ channel (Kv1.5) cloned from rabbit heart and facilitation of inactivation of the delayed rectifier current by β subunit" FEBS Lett.372. 20-24 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Ishii, K.: "The amino acid residues responsible for sensitivity to pH of cloned K^+ channels" Heart Vessels. Supple.9. 12-13 (1995)

    • Related Report
      1995 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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