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A Current Regulation by Dipeptidyl Peptidase-Like Proteins

A Current Regulation by Dipeptidyl Peptidase-Like Proteins
二肽基肽酶样蛋白的当前调控
批准号:
8210841
负责人:
Paul Pfaffinger
金额:
$30.39万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-01-01 至 2013-12-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A Current Regulation by Dipeptidyl Peptidase-Like Proteins Dipeptidyl peptidase like (DPL) proteins, DPP6 and DPP10, regulate Kv4 channel expression and functional properties and are essential components of the native neuronal ISA, somatodendritic A current along with Kv4 alpha subunits and KChIP auxiliary subunits. Without DPL expression, ISA is severely disrupted with reduced current expression and abnormal activation and inactivation properties. In this project we will test the hypothesis that specific conserved functional domains in the first two exons of DPL genes regulate the interaction of DPL proteins with Kv4 channels proteins and determine the functional properties of the channel complex. These studies will provide important new information about the molecular mechanisms that regulate the functional properties of neurons and likely will be important for our understanding of the molecular mechanisms underlying disease processes such as ALS, autism spectrum disorder, asthma, and other regulatory pathways that DPL proteins have been implicated in. In this project we will address the following aims to better understand the molecular mechanisms involved in the regulation of A currents by DPL proteins. Aim 1: Test the hypothesis that DPP6a and DPP10a accelerate inactivation using a novel N-terminal motif that shares a common underlying molecular mechanism with other N-type inactivation domains. Aim 2: Test the Hypothesis that multiple intermediate states are experienced during N-type inactivation by DPP6a and DPP10a. Aim 3: Test the hypothesis that specific DPL residues in transmembrane and peri-transmembrane region modulate Kv4 channel activation gating. PUBLIC HEALTH RELEVANCE: Dipeptidyl peptidase-like (DPL) proteins are expressed at high levels in the brain and human genetic linkage studies have linked DPL genetic variations to asthma, amyotropic lateral sclerosis, and autism spectrum disorders. A known function of DPL proteins is to bind and regulate potassium channels. In this project we will characterize the molecular mechanisms that underlie the regulation of potassium channels by DPL proteins.
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The integrated stress response in cognitive disorders
  • 批准号:
    10673598
  • 项目类别:
  • 资助金额:
    $88.43万
  • 财政年份:
    2012
  • 负责人:
    Paul Pfaffinger
  • 依托单位:
A Current Regulation by Dipeptidyl Peptidase-Like Proteins
  • 批准号:
    8401534
  • 项目类别:
  • 资助金额:
    $29.33万
  • 财政年份:
    2010
  • 负责人:
    Paul Pfaffinger
  • 依托单位:
A Current Regulation by Dipeptidyl Peptidase-Like Proteins
  • 批准号:
    8006390
  • 项目类别:
  • 资助金额:
    $30.39万
  • 财政年份:
    2010
  • 负责人:
    Paul Pfaffinger
  • 依托单位:
A Current Regulation by Dipeptidyl Peptidase-Like Proteins
  • 批准号:
    7768780
  • 项目类别:
  • 资助金额:
    $30.7万
  • 财政年份:
    2010
  • 负责人:
    Paul Pfaffinger
  • 依托单位:
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