CNS L PROLINE TRANSPORTER

中枢神经系统 L 脯氨酸转运蛋白

基本信息

  • 批准号:
    2839363
  • 负责人:
  • 金额:
    $ 23.87万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1993
  • 资助国家:
    美国
  • 起止时间:
    1993-12-15 至 2000-11-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION: (Applicant's abstract) The mammalian, brain-specific, high affinity L-proline transporter (PROT) is a member of a gene family of Na and Cl dependent plasma membrane transport proteins that includes transporters for several neurotransmitters, osmolytes, and metabolites. This novel transporter is expressed in subpopulations of putative glutamatergic neurons, where the PROT protein is enriched in synaptic vesicles. These findings warrant the consideration of a presynaptic regulatory role for PROT in excitatory transmission at specific glutamatergic nerve terminals. The long term objective of the research is to elucidate the physiological role of mammalian brain PROT in excitatory synaptic transmission. Specific aim 1 will investigate the functional role for PROT in synaptic vesicles. PROT is the only protein characterized at the molecular level that is specifically localized to synaptic vesicles in excitatory nerve terminals. The applicant will immunoisolate the PROT-containing synaptic vesicles and examine the neurotransmitter phenotype and biochemical properties of this unique subpopulation of synaptic vesicles. Are the PROT-containing vesicles prolinergic or glutamatergic, or do they represent a discrete set of excitatory nerve terminal vesicles with an unprecedented function? Little is known about how proteins are targeted to synaptic vesicles. Specific aim 2 will use recombinant DNA techniques to identify putative synaptic vesicle targeting signals in PROT. Preliminary studies indicate that the primary amino acid sequence of PROT contains information necessary for targeting this protein to intracellular vesicles. Finally, the precise substrate binding site has not been identified or any member of this transporter family. Several recent advances indicate that PROT is a good model system to elucidate this critical region of the transporter protein. Specific aim 3 will delineate the substrate binding domain and/or the translocation pore of PROT. The findings may provide new insights into presynaptic regulatory mechanisms involved in synaptic plasticity and excitotoxic nerve cell damage.
描述:(申请人摘要)哺乳动物,脑特异性,高

项目成果

期刊论文数量(5)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Characterization and distribution of the neuronal glutamate transporter EAAC1 in rat brain.
  • DOI:
    10.1152/ajpcell.1996.270.1.c67
  • 发表时间:
    1996
  • 期刊:
  • 影响因子:
    0
  • 作者:
    M. Velaz-Faircloth;T. S. McGraw;M. S. alandro;R. Fremeau;M. Kilberg;K. Anderson
  • 通讯作者:
    M. Velaz-Faircloth;T. S. McGraw;M. S. alandro;R. Fremeau;M. Kilberg;K. Anderson
A novel nonopioid action of enkephalins: competitive inhibition of the mammalian brain high affinity L-proline transporter.
脑啡肽的一种新型非阿片类药物作用:竞争性抑制哺乳动物大脑高亲和力 L-脯氨酸转运蛋白。
  • DOI:
  • 发表时间:
    1996
  • 期刊:
  • 影响因子:
    0
  • 作者:
    FremeauJr,RT;Velaz-Faircloth,M;Miller,JW;Henzi,VA;Cohen,SM;Nadler,JV;Shafqat,S;Blakely,RD;Domin,B
  • 通讯作者:
    Domin,B
Mammalian brain-specific L-proline transporter. Neuronal localization of mRNA and enrichment of transporter protein in synaptic plasma membranes.
哺乳动物脑特异性 L-脯氨酸转运蛋白。
  • DOI:
    10.1074/jbc.270.26.15755
  • 发表时间:
    1995
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Velaz-Faircloth,M;Guadaño-Ferraz,A;Henzi,VA;FremeauJr,RT
  • 通讯作者:
    FremeauJr,RT
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

ROBERT T FREMEAU其他文献

ROBERT T FREMEAU的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('ROBERT T FREMEAU', 18)}}的其他基金

CNS L-PROLINE TRANSPORTER
CNS L-脯氨酸转运蛋白
  • 批准号:
    2270738
  • 财政年份:
    1993
  • 资助金额:
    $ 23.87万
  • 项目类别:
CNS L-PROLINE TRANSPORTER
CNS L-脯氨酸转运蛋白
  • 批准号:
    2270736
  • 财政年份:
    1993
  • 资助金额:
    $ 23.87万
  • 项目类别:
CNS L PROLINE TRANSPORTER
中枢神经系统 L 脯氨酸转运蛋白
  • 批准号:
    2609659
  • 财政年份:
    1993
  • 资助金额:
    $ 23.87万
  • 项目类别:
CNS L PROLINE TRANSPORTER
中枢神经系统 L 脯氨酸转运蛋白
  • 批准号:
    2037749
  • 财政年份:
    1993
  • 资助金额:
    $ 23.87万
  • 项目类别:
CNS L-PROLINE TRANSPORTER
CNS L-脯氨酸转运蛋白
  • 批准号:
    2270737
  • 财政年份:
    1993
  • 资助金额:
    $ 23.87万
  • 项目类别:
TRANSSYNAPTIC REGULATION OF PROENKEPHALIN A GENE TRANSCR
脑啡肽原 A 基因转录的跨突触调节
  • 批准号:
    3054033
  • 财政年份:
    1986
  • 资助金额:
    $ 23.87万
  • 项目类别:
TRANSSYNAPTIC REGULATION OF PROENKEPHALIN A GENE TRANSCR
脑啡肽原 A 基因转录的跨突触调节
  • 批准号:
    3054032
  • 财政年份:
    1985
  • 资助金额:
    $ 23.87万
  • 项目类别:

相似海外基金

Non-canonical chimeric proteins generated during Adenovirus infection
腺病毒感染期间产生的非典型嵌合蛋白
  • 批准号:
    10448505
  • 财政年份:
    2021
  • 资助金额:
    $ 23.87万
  • 项目类别:
Non-canonical chimeric proteins generated during Adenovirus infection
腺病毒感染期间产生的非典型嵌合蛋白
  • 批准号:
    10312411
  • 财政年份:
    2021
  • 资助金额:
    $ 23.87万
  • 项目类别:
Increasing efficiency in formation of chimeric proteins
提高嵌合蛋白形成的效率
  • 批准号:
    561998-2021
  • 财政年份:
    2021
  • 资助金额:
    $ 23.87万
  • 项目类别:
    University Undergraduate Student Research Awards
Decoration and Dimerization of Chimeric Proteins Mediated by Coiled-Coil Interactions
卷曲螺旋相互作用介导的嵌合蛋白的修饰和二聚化
  • 批准号:
    537306-2018
  • 财政年份:
    2019
  • 资助金额:
    $ 23.87万
  • 项目类别:
    Collaborative Research and Development Grants
Exploring the therapeutic potential of chimeric proteins
探索嵌合蛋白的治疗潜力
  • 批准号:
    1947736
  • 财政年份:
    2017
  • 资助金额:
    $ 23.87万
  • 项目类别:
    Studentship
TARGETING PROTEIN INTERACTIONS AND DESIGNING CHIMERIC PROTEINS
靶向蛋白质相互作用并设计嵌合蛋白质
  • 批准号:
    8364271
  • 财政年份:
    2011
  • 资助金额:
    $ 23.87万
  • 项目类别:
Therapeutic peanut allergen Fc gamma chimeric proteins to treat peanut allergy
用于治疗花生过敏的治疗性花生过敏原 Fc γ 嵌合蛋白
  • 批准号:
    8444422
  • 财政年份:
    2010
  • 资助金额:
    $ 23.87万
  • 项目类别:
Cat allergen-human Fc-gamma1 chimeric proteins to treat cat allergy
猫过敏原-人Fc-gamma1嵌合蛋白治疗猫过敏
  • 批准号:
    7907314
  • 财政年份:
    2010
  • 资助金额:
    $ 23.87万
  • 项目类别:
TARGETING PROTEIN INTERACTIONS AND DESIGNING CHIMERIC PROTEINS
靶向蛋白质相互作用并设计嵌合蛋白质
  • 批准号:
    8171849
  • 财政年份:
    2010
  • 资助金额:
    $ 23.87万
  • 项目类别:
Therapeutic peanut allergen Fc gamma chimeric proteins to treat peanut allergy
用于治疗花生过敏的治疗性花生过敏原 Fc γ 嵌合蛋白
  • 批准号:
    8313432
  • 财政年份:
    2010
  • 资助金额:
    $ 23.87万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了