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Roles and mechanisms of Slo and Slack Channels in Brain

Roles and mechanisms of Slo and Slack Channels in Brain
Slo 和 Slack 通道在大脑中的作用和机制
批准号:
6935322
负责人:
LEONARD K KACZMAREK
金额:
$155.74万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-04 至 2006-08-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A class of calcium-activated potassium channels termed BK(Ca) channels are enriched at presynaptic neurotransmitter release sites within the brain, and are believed to control both the amount and timing of neurotransmitter release. BK(Ca) channels are encoded by the Slo gene. Recent evidence suggests that a related gene, Slack, also contributes to BK(Ca)-like channels in neurons, and that some BK(Ca) channels may be comprised of heteromultimers of Slo and Slack channels subunits. The experiments in this proposal will characterize the molecular, biophysical and structural properties of BK(Ca) channels in both the somata and presynaptic terminals of native neurons, and in transfected cells. The role of the Slo and Slack channel subunits in normal synaptic transmission, and the mechanisms of their response to hypoxia, will be determined by patch clamp measurements coupled with genetic knockout approaches. The structure and function of the large carboxy-terminal regulatory region of the Slo channel subunit with its calcium-binding sites, and its interaction with other proteins, including the Slack subunit, will be determined by biophysical and biochemical measurements and by X-ray crystallographic methods. Finally the structure of intact BK(Ca) channels will be determined by cryo-electronmicroscopy. Knowledge of the molecular properties and regulation of BK(Ca) channels in normal and hypoxic neurons, together with structural determinations of their interactions with both drugs and natural ligands, will be key in the development of more effective treatments for disorders such as epilepsy and stroke.
期刊论文(10)
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会议论文
Effect of phosphatidylserine on unitary conductance and Ba2+ block of the BK Ca2+-activated K+ channel: re-examination of the surface charge hypothesis.
磷脂酰丝氨酸对BK Ca2+活化的K+通道的单位电导和BA2+块的影响:表面电荷假说的重新检查。
DOI: 10.1085/jgp.200208746
发表时间: 2003-05
期刊: JOURNAL OF GENERAL PHYSIOLOGY
影响因子: 3.8
作者: [Park, Jin Bong, Kim, Hee Jeong, Ryu, Pan Dong, Moczydlowski, Edward]
通讯作者: Moczydlowski, Edward
DOI: 10.1085/jgp.200509323
发表时间: 2005-09
期刊: The Journal of general physiology
影响因子: --
作者: [Krishnan MN, Bingham JP, Lee SH, Trombley P, Moczydlowski E]
通讯作者: Moczydlowski E
DOI: 10.1085/jgp.200509368
发表时间: 2005-11
期刊: The Journal of general physiology
影响因子: --
作者: [Giraldez T, Hughes TE, Sigworth FJ]
通讯作者: Sigworth FJ
Calcium influx via L- and N-type calcium channels activates a transient large-conductance Ca2+-activated K+ current in mouse neocortical pyramidal neurons.
通过 L 型和 N 型钙通道的钙流入会激活小鼠新皮质锥体神经元中的瞬时大电导 Ca2 激活 K 电流。
DOI: 10.1523/jneurosci.23-09-03639.2003
发表时间: 2003
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Sun,Xiaolu, Gu,XiangQ, Haddad,GabrielG]
通讯作者: Haddad,GabrielG
7
    Cellular Regulation of Sodium-activated Potassium Channels
    • 批准号:
      10358638
    • 项目类别:
    • 资助金额:
      $36.64万
    • 财政年份:
      2018
    • 负责人:
      LEONARD K KACZMAREK
    • 依托单位:
    Cellular Regulation of Sodium-activated Potassium Channels
    • 批准号:
      10584753
    • 项目类别:
    • 资助金额:
      $43.07万
    • 财政年份:
      2018
    • 负责人:
      LEONARD K KACZMAREK
    • 依托单位:
    Cellular regulation of Sodium-activated Ion Channels
    • 批准号:
      8185062
    • 项目类别:
    • 资助金额:
      $35.17万
    • 财政年份:
      2011
    • 负责人:
      LEONARD K KACZMAREK
    • 依托单位:
    Cellular regulation of Sodium-activated Ion Channels
    • 批准号:
      8706194
    • 项目类别:
    • 资助金额:
      $34.18万
    • 财政年份:
      2011
    • 负责人:
      LEONARD K KACZMAREK
    • 依托单位:
    海外基金