GLUTAMATE RECEPTOR FUNCTION BY THE NR1 5TH EXON
GLUTAMATE RECEPTOR FUNCTION BY THE NR1 5TH EXON
批准号:
2858170
负责人:
Stephen F Traynelis
金额:
$10.37万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-01-01 至 2000-12-31
关键词:
RNA splicing Xenopus oocyte cerebral ischemia /hypoxia complementary DNA gene mutation glutamate receptor glutamates hippocampus hydrogen immunocytochemistry lactate dehydrogenases neuropharmacology peptide analog polyamines polymerase chain reaction protein sequence protein structure function recombinant proteins site directed mutagenesis spermidine structural genes transfection voltage /patch clamp zinc
中文摘要
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英文摘要
Intense interest has focused on the NMDA subtype of glutamate receptor
because of its roles in development, synaptic transmission, memory, and
pathological situations such as ischemia and epilepsy. Although NMDA
receptors are modulated by many endogenous substances, the control of
receptor function by physiological concentrations of protons is
particularly important, not only because the interstitial pH is highly
dynamic, but also because of the extracellular acidification that
accompanies ischemia and seizures. These perturbations in pH could serve
as negative feedback to inhibit NMDA receptor function, and thereby limit
seizure duration or glutamate-mediated damage during ischemia. My
preliminary studies have shown that the 5th alternative exon of the NR1
subunit renders receptors proton-insensitive, and this effect can be
mimicked by endogenous polyamines. This finding provides an opportunity to
approach proton control of NMDA receptor function in structural terms, and
additionally raises the possibility that the different splice variants of
the NMDA receptor might be related to the selective vulnerability of
central structures to ischemia-induced damage or seizure initiation. The
long-term objective of this project is to determine at the structural and
functional level how the 5th NR1 exon controls receptors in normal and
pathological situations. The five main goals are:
(1) To identify the structural determinants within the NR1 5th exon that
control proton inhibition.
(2) To determine at the biophysical level how the NR1 5th exon controls
the receptor's proton sensitivity.
(3) To identify compounds that modulate the NMDA receptor's proton
sensitivity, and determine whether these compounds exert their effects in
a manner similar to the 5th exon.
(4) To investigate the link between the proton sensitivity of recombinant
NMDA receptor splice variants and their cytotoxic potential.
(5) To determine whether the 5th exon is differentially expressed in the
central nervous system.
These experiments will help to explain at the structural, anatomical, and
functional levels how the 5th exon influences receptor function. In
addition, these experiments will help to define an important regulatory
site on the NMDA receptor, and identify compounds that act at that site.
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Genetic analysis to determine the functional role of GRID1
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批准号:10217304
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项目类别:
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资助金额:$15.6万
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财政年份:2021
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负责人:Stephen F Traynelis
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依托单位:
Glutamate receptors and human neurological disease
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批准号:10392917
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项目类别:
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资助金额:$76.81万
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财政年份:2019
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负责人:Stephen F Traynelis
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依托单位:
Glutamate receptors and human neurological disease
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批准号:10153899
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项目类别:
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资助金额:$76.06万
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财政年份:2019
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负责人:Stephen F Traynelis
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依托单位:
Glutamate receptors and human neurological disease
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批准号:10608949
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项目类别:
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资助金额:$76.81万
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财政年份:2019
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负责人:Stephen F Traynelis
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依托单位:
Glutamate receptors and human neurological disease
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批准号:9923776
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项目类别:
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资助金额:$74.52万
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财政年份:2019
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负责人:Stephen F Traynelis
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依托单位:
Functional effects of ion channel mutations found via exome sequencing
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批准号:9193444
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项目类别:
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资助金额:$26.12万
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财政年份:2016
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负责人:Stephen F Traynelis
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依托单位:
Optimization of small molecule probes
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批准号:8440355
-
项目类别:
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资助金额:$22.46万
-
财政年份:2012
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负责人:Stephen F Traynelis
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依托单位:
Optimization of small molecule probes
-
批准号:8299822
-
项目类别:
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资助金额:$23.33万
-
财政年份:2012
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负责人:Stephen F Traynelis
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依托单位:
Control of AMPA receptor function by phosphorylation
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批准号:8213435
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项目类别:
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资助金额:$33.23万
-
财政年份:2010
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负责人:Stephen F Traynelis
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依托单位:
Control of AMPA receptor function by phosphorylation
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批准号:8015207
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项目类别:
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资助金额:$33.23万
-
财政年份:2010
-
负责人:Stephen F Traynelis
-
依托单位:
Control of AMPA receptor function by phosphorylation
-
批准号:7565237
-
项目类别:
-
资助金额:$33.91万
-
财政年份:2010
-
负责人:Stephen F Traynelis
-
依托单位:
Control of AMPA receptor function by phosphorylation
-
批准号:8415573
-
项目类别:
-
资助金额:$32.07万
-
财政年份:2010
-
负责人:Stephen F Traynelis
-
依托单位:
Mechanism of action of novel subunit-selective NMDA receptor modulators
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批准号:8240504
-
项目类别:
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资助金额:$33.23万
-
财政年份:2009
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负责人:Stephen F Traynelis
-
依托单位:
Mechanism of Action of Novel Subunit-Selective NMDA Receptor Modulators
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批准号:8730715
-
项目类别:
-
资助金额:$33.78万
-
财政年份:2009
-
负责人:Stephen F Traynelis
-
依托单位:
Mechanism of action of novel subunit-selective NMDA receptor modulators
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批准号:8045409
-
项目类别:
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资助金额:$33.23万
-
财政年份:2009
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负责人:Stephen F Traynelis
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依托单位:
Mechanism of Action of Novel Subunit-Selective NMDA Receptor Modulators
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批准号:8639023
-
项目类别:
-
资助金额:$34.13万
-
财政年份:2009
-
负责人:Stephen F Traynelis
-
依托单位:
Mechanism of Action of Novel Subunit-Selective NMDA Receptor Modulators
-
批准号:9112009
-
项目类别:
-
资助金额:$34.13万
-
财政年份:2009
-
负责人:Stephen F Traynelis
-
依托单位:
Mechanism of action of novel subunit-selective NMDA receptor modulators
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批准号:7644170
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项目类别:
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资助金额:$33.91万
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财政年份:2009
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负责人:Stephen F Traynelis
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依托单位:
Identification of ligands that bind to the orphan delta2 receptor
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批准号:7588965
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项目类别:
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资助金额:$20.34万
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财政年份:2008
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负责人:Stephen F Traynelis
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依托单位:
Identification of protease activated receptor-2 modulators
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批准号:7170095
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项目类别:
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资助金额:$19.13万
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财政年份:2006
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负责人:Stephen F Traynelis
-
依托单位:
海外基金