STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
批准号:
2771872
负责人:
JAMES J LAH
金额:
$10.72万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-09-01 至 2001-08-31
关键词:
Alzheimer's disease Caenorhabditis elegans amyloid proteins antibody brain cell cell type complementary DNA electron microscopy immunocytochemistry laboratory rabbit laboratory rat light microscopy mutant protein isoforms protein structure function tissue /cell culture transfection western blottings
中文摘要
最近发现与早发性家族性痴呆相关的基因
英文摘要
The recent identification of genes associated with early -onset familial
Alzheimer's disease (FAD) opens new and exciting avenues of investigation
into the pathogenesis of this devastating and incurable cause of dementia.
The first gene to be identified, S182, may be responsible for many of the
chromosome 14 associated cases of FAD. Subsequent reports identifying a
homologous gene, STM2, implicated in chromosome 1 associated FAD are
perhaps most remarkable for the fact that these two genes have begun to
define a new gene family which is important in the pathogenesis of
Alzheimer's disease. There are two other known members of this family
which have been identified in Caenorhabditis elegans. The amino acid
sequences and the putative structure of the four proteins are closely
related and suggest that they may share functional similarities.
In this proposal, we outline a series of experiments and hypotheses which
will begin to critically analyze the function of these proteins. In
Specific Aim 1, we propose the production of a series of isoform- and
domain-specific antibodies to S182 and STM2. These antibodies are being
designed to allow their use in addressing several specific hypotheses in
subsequent Specific Aims. We present the results of some Preliminary
Studies which demonstrate the successful production of the antibody to
S182. In Specific Aims 2 and 3, we will exploit these antibodies to pursue
questions regarding the distribution and structure of these proteins. In
the final Specific Aim, we will investigate the possible functional
relationship between S182 and STM2 and the C. elegans protein SPE-4. These
experiments will attempt to phenotypically rescue loss of function spe-4
mutants through the introduction of human S182 and STM2 sequences.
In addition to these research activities, this proposal is being submitted
as part of an overall plan of training and career development. Activities
are outlined over a five year period which will provide the Principal
Investigator with a unique opportunity to development as a research
scientist and help to insure his success in academic neurology.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Translation of GluN2B-selective PET radiopharmaceuticals in Alzheimers patients
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批准号:10716786
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项目类别:
-
资助金额:$78.25万
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财政年份:2023
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负责人:JAMES J LAH
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依托单位:
The Emory Healthy Brain Study: Discovering Predictive Biomarkers for Alzheimer's Disease
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批准号:10348719
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项目类别:
-
资助金额:$713.81万
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财政年份:2021
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负责人:JAMES J LAH
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依托单位:
The Emory Healthy Brain Study: Discovering Predictive Biomarkers for Alzheimer's Disease
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批准号:10555203
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项目类别:
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资助金额:$701.17万
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财政年份:2021
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负责人:JAMES J LAH
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依托单位:
Emory Alzheimer's Disease Research Center
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批准号:10408021
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项目类别:
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资助金额:$46.88万
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财政年份:2020
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负责人:JAMES J LAH
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依托单位:
Emory Alzheimer's Disease Research Center
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批准号:10673939
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项目类别:
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资助金额:$46.88万
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财政年份:2020
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负责人:JAMES J LAH
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依托单位:
Emory Alzheimer's Disease Research Center
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批准号:10212229
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项目类别:
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资助金额:$46.88万
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财政年份:2020
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负责人:JAMES J LAH
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依托单位:
Core B: Clinical Core
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批准号:9280777
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项目类别:
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资助金额:$39.33万
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财政年份:2005
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负责人:JAMES J LAH
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依托单位:
CLINICAL CORE
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批准号:8441017
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项目类别:
-
资助金额:$42.49万
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财政年份:2005
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负责人:JAMES J LAH
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依托单位:
Core B: Clinical Core
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批准号:8849139
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项目类别:
-
资助金额:$37.43万
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财政年份:2005
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负责人:JAMES J LAH
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依托单位:
ApoE Receptor LR11 in Alzheimer's Etiopathogenesis
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批准号:6811586
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项目类别:
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资助金额:$30.98万
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财政年份:2004
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负责人:JAMES J LAH
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依托单位:
ApoE Receptor LR11 in Alzheimer's Etiopathogenesis
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批准号:7110266
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项目类别:
-
资助金额:$30.25万
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财政年份:2004
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负责人:JAMES J LAH
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依托单位:
ApoE Receptor LR11 in Alzheimer's Etiopathogenesis
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批准号:7256942
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项目类别:
-
资助金额:$29.38万
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财政年份:2004
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负责人:JAMES J LAH
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依托单位:
ApoE Receptor LR11 in Alzheimer's Etiopathogenesis
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批准号:6933148
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项目类别:
-
资助金额:$30.98万
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财政年份:2004
-
负责人:JAMES J LAH
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依托单位:
STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
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批准号:2891411
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项目类别:
-
资助金额:$10.72万
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财政年份:1996
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负责人:JAMES J LAH
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依托单位:
STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
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批准号:2260109
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项目类别:
-
资助金额:$7.85万
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财政年份:1996
-
负责人:JAMES J LAH
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依托单位:
STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
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批准号:6188239
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项目类别:
-
资助金额:$10.95万
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财政年份:1996
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负责人:JAMES J LAH
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依托单位:
STRUCTURE AND FUNCTION OF ALZHEIMERS DISEASE PROTEINS
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批准号:2519886
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项目类别:
-
资助金额:$8.93万
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财政年份:1996
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负责人:JAMES J LAH
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依托单位:
CLINICAL CORE
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批准号:8662663
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项目类别:
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资助金额:$36.18万
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财政年份:--
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负责人:JAMES J LAH
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依托单位:
Determinants of Neurodegeneration in the Evolution of MCI and AD
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批准号:8962189
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项目类别:
-
资助金额:$13.74万
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财政年份:--
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负责人:JAMES J LAH
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依托单位:
CLINICAL CORE
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批准号:8014463
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项目类别:
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资助金额:$37.18万
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财政年份:--
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负责人:JAMES J LAH
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依托单位:
国内基金
海外基金
犬钩虫中Caenorhabditis elegans daf同源基因的鉴定和功能研究
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批准号:30972181
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项目类别:面上项目
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资助金额:30.0万元
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批准年份:2009
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负责人:杨玉荣
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依托单位:
利用线虫(Caenorhabditis elegans)模型研究14-3-3蛋白在机体抵御逆境因子胁迫过程中的分子作用机制
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批准号:30771234
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项目类别:面上项目
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资助金额:30.0万元
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批准年份:2007
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负责人:王亚梅
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依托单位: