Caspase-2 Probe Compounds
Caspase-2 Probe Compounds
批准号:
10322438
负责人:
Karen H Ashe
金额:
$71.04万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-02-15 至 2023-11-30
关键词:
AMPA ReceptorsAccelerationAlzheimer&aposs DiseaseAlzheimer&aposs disease brainAnimal ModelBindingBiological AssayBiological MarkersBiological ModelsBiologyBrainCASP2 geneCaspaseCellsChemicalsCognitionCognitiveCognitive deficitsCollectionCommunitiesCrystallographyCytoskeletal ProteinsDendritic SpinesDevelopmentDockingFamilyFrontotemporal DementiaFunctional disorderGlaucomaGoalsHealthHumanHuntington DiseaseHuntington geneImpaired cognitionIn VitroIndustry StandardMeasurementMeasuresMediatingModelingModificationMolecularMusNational Center for Advancing Translational SciencesNerve DegenerationNeuroblastomaNeurodegenerative DisordersNeurologicNeuronsOxidative StressParkinson DiseasePeptide HydrolasesPharmaceutical ChemistryPharmaceutical PreparationsPharmacologic SubstancePharmacologyProteinsProteolysisResearchResearch PersonnelRoleScientistSeriesSiteSpecificityStrokeStructure-Activity RelationshipSynapsesSynaptic MembranesSynaptic TransmissionSynaptic plasticitySystemTauopathiesTestingTherapeuticTherapeutic AgentsTransgenic OrganismsTranslational ResearchUnited States National Institutes of HealthWorkagedanalogbaseclinically relevantcognitive functiondesigndisease phenotypeexcitotoxicityfollow-upimprovedin vivoin vivo Modelinhibitorinnovationmorris water mazemultidisciplinarymutantnervous system disorderneurophysiologynovel therapeuticspostsynapticpreclinical studypreservationpreventreceptor functionrepairedside effectsmall moleculestructural biologysynaptic functiontau Proteinstherapeutic developmenttherapeutic targettool
中文摘要
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英文摘要
Project Summary Abstract
Caspase-2 has been implicated in neurological indications such as stroke, Alzheimer's, Parkinson's, and
Huntington's diseases, neuroblastoma, neuro-ophthalomology, and frontotemporal dementia. The broad, long-
term objective of our work is the development of specific caspase-2 inhibitors as neuro-therapeutic agents. This
long-term objective hinges on first developing caspase-2 probes that will allow us to show that specific
pharmacological reduction of caspase-2 activity by small molecule probes leads to the amelioration of disease
phenotype, initially in animal models. Our specific aims all target the discovery and development of caspase-2
probes but each has a different starting point. We will use measurement of ∆tau314 levels, a specific
therapeutically- and clinically-relevant biomarker, as part of our testing funnel, to gauge the efficacy of our probes
in cells. Our probe design and development will feature three parallel paths of compound characterization and
optimization, each of which will inform the other as to caspase-2 binding that influences specificity and potency.
Our three aims are to develop (1) probes from proteins that are specifically cleaved by caspase-2, (2) probes
from HTS follow-on, and (3) probes from known selective caspase-2 inhibitors. Our goal in each of these is to
produce a probe or tool compound which has in vitro potency <100 nM at the target protein, possesses >30-fold
selectivity relative to sequence-related targets in the same family, has been profiled against an “industry-
standard” panel of pharmacologically-relevant off-targets, and has demonstrated on-target effect in cells of <1
µM. To demonstrate in vivo relevance, we will test these probes in rTg4510 mice using the Morris water maze,
a well-established model of cognition. We expect that these probes that specifically target caspase-2 will restore
cognition in these aged mice without observable side effects. Ultimately, we will use these specific caspase-2
probes to investigate the broad range of neurological disorders in which caspase-2 activity has been implicated.
This will constitute and important vertical advancement and spur the pharmaceutical development of therapeutics
that will positively impact human health.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Prodrugs of potent and selective protease inhibitors as tauopathy therapeutics
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批准号:10761291
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项目类别:
-
资助金额:$35.0万
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财政年份:2023
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负责人:Karen H Ashe
-
依托单位:
Caspase-2 Probe Compounds
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批准号:10532777
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项目类别:
-
资助金额:$70.96万
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财政年份:2019
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负责人:Karen H Ashe
-
依托单位:
Caspase-2 Probe Compounds
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批准号:9974861
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项目类别:
-
资助金额:$36.97万
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财政年份:2019
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负责人:Karen H Ashe
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依托单位:
Molecular endophenotypes of H1 and H2 MAPT haplotypes
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批准号:9762819
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项目类别:
-
资助金额:$19.25万
-
财政年份:2018
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负责人:Karen H Ashe
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依托单位:
Role of Tau Cleavage in Tauopathy
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批准号:8798702
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项目类别:
-
资助金额:$36.12万
-
财政年份:2013
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负责人:Karen H Ashe
-
依托单位:
Role of Tau Cleavage in Tauopathy
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批准号:8503061
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项目类别:
-
资助金额:$41.14万
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财政年份:2013
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负责人:Karen H Ashe
-
依托单位:
Role of Tau Cleavage in Tauopathy
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批准号:8617878
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项目类别:
-
资助金额:$40.84万
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财政年份:2013
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负责人:Karen H Ashe
-
依托单位:
Role of Tau Cleavage in Tauopathy
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批准号:8999021
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项目类别:
-
资助金额:$36.22万
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财政年份:2013
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负责人:Karen H Ashe
-
依托单位:
Improved Transgenic Mouse Model of Alzheimer's Disease
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批准号:8244853
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项目类别:
-
资助金额:$0.0万
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财政年份:2012
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负责人:Karen H Ashe
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依托单位:
Improved Transgenic Mouse Model of Alzheimer's Disease
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批准号:8413428
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项目类别:
-
资助金额:$0.0万
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财政年份:2012
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负责人:Karen H Ashe
-
依托单位:
Specific amyloid-beta oligomer aptamers
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批准号:7937928
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项目类别:
-
资助金额:$36.9万
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财政年份:2009
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负责人:Karen H Ashe
-
依托单位:
Specific amyloid-beta oligomer aptamers
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批准号:7815825
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项目类别:
-
资助金额:$36.98万
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财政年份:2009
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负责人:Karen H Ashe
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依托单位:
In Search of the Molecular Basis of Memory Loss in Tauopathy
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批准号:7678928
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项目类别:
-
资助金额:$29.65万
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财政年份:2008
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负责人:Karen H Ashe
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依托单位:
In Search of the Molecular Basis of Memory Loss in Tauopathy
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批准号:7514358
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项目类别:
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资助金额:$29.23万
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财政年份:2008
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负责人:Karen H Ashe
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依托单位:
In Search of the Molecular Basis of Memory Loss in Tauopathy
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批准号:8025924
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项目类别:
-
资助金额:$29.34万
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财政年份:2008
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负责人:Karen H Ashe
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依托单位:
The Biology of Alzheimer's Disease in Transgenic Mice
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批准号:7118110
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项目类别:
-
资助金额:$50.36万
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财政年份:2004
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负责人:Karen H Ashe
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依托单位:
The Biology of Alzheimer's Disease in Transgenic Mice
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批准号:7473182
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项目类别:
-
资助金额:$50.84万
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财政年份:2004
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负责人:Karen H Ashe
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依托单位:
The Biology of Alzheimer's Disease in Transgenic Mice
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批准号:6950460
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项目类别:
-
资助金额:$49.82万
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财政年份:2004
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负责人:Karen H Ashe
-
依托单位:
The Biology of Alzheimer's Disease in Transgenic Mice
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批准号:7273551
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项目类别:
-
资助金额:$50.37万
-
财政年份:2004
-
负责人:Karen H Ashe
-
依托单位:
The Biology of Alzheimer's Disease in Transgenic Mice
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批准号:6951105
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项目类别:
-
资助金额:$50.07万
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财政年份:2004
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负责人:Karen H Ashe
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依托单位:
海外基金