Inhibition of Neurotransmission in Specific Neuronal Populations
Inhibition of Neurotransmission in Specific Neuronal Populations
批准号:
7482543
负责人:
Douglas A Lappi
金额:
$11.43万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2009-04-30
关键词:
Alzheimer&aposs DiseaseAnimalsBindingBiologicalBiological AssayBiological ModelsBiological ProcessBreathingCatalogingCatalogsCell DeathCell Surface ReceptorsCell membraneCell physiologyCell surfaceCellsComplexDataDiseaseEndocytosisEndosomesEnzymesEvaluationGlycoproteinsGovernmentHomeostasisHyperalgesiaLightLinkMethodsModelingNarcolepsyNervous system structureNeuronsNeuropeptidesNeurotransmittersPathologicPersonsPhasePlayPopulationPositioning AttributeProcessPubMedPublicationsPurposeReagentRegulationResearchResearch PersonnelRibosomesRoleSNAP receptorScientistSeriesSorting - Cell MovementSubstance PSubstance P ReceptorSurface AntigensSystemSystems BiologyTargeted ToxinsTechniquesTechnologyTestingTherapeuticTimeToxinVesicleWorkallodyniaanalogbasebotulinumbotulinum toxin type Cbotulinum toxin type Ecell typechemical conjugatechronic paincommercializationconceptdaydrug developmentexpression cloninginnovative technologiesinternal controlneuropsychiatryneurotransmissionneurotransmitter releasenew technologypreventreceptorresearch studysubstance P-saporintool
中文摘要
描述(由申请人提供):在过去十年的广泛工作中,很明显,生物学
英文摘要
DESCRIPTION (provided by applicant): In extensive work over the last decade, it has become clear that biologically
active molecules can be inserted into specific cell types through targeting to molecules on the cell surface. It is here proposed to direct this technology to specific neuronal cell types with the purpose of temporarily inhibiting their capacity of releasing neurotransmitters. As proof of concept, it is proposed to synthesize a conjugate of the neuropeptide substance P and the enzymatic (light) chain of botulinum toxin from C. botulinum strain E (BTELC) and examine the effects on cells that express both the substance P receptor and SNAP-25, the substrate for the enzymatic activity of BTELC. SNAP-25 is an essential player in neurotransmitter release, and its cleavage by BTELC would prevent release. Entry into a specific cell type would be provided by the substance P moiety, since only binding to its receptor would cause internalization. The process requires the cloning and expression of BTELC and the synthesis of a
substance P analog that would allow conjugation.
Inhibition of neurotransmitter release would be a short-term phenomenon, because slowly over time SNAP-25 would be re-synthesized and re-occupy its original position in the SNARE complex that is necessary for release. This would be an approximately one-month process.
The demonstration of efficacy would usher in a new technology with applications as research reagents. Targeted BTELC could be used to shut down neuronal subtypes, allowing observation of the effect and greater understanding of the function of the cell in systems biology, while the return to homeostasis and function would act as a
control for the experiment. Therapeutic applications for the treatment of neuropsychiatric and other maladies could result from this technology, but are not the focus of this application.
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