Enzymes involved in neuropeptide biosynthesis and regulation
Enzymes involved in neuropeptide biosynthesis and regulation
批准号:
8050620
负责人:
Lakshmi A Devi
金额:
$35.22万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-08-01 至 2014-04-30
关键词:
Addictive BehaviorAffectAlzheimer&aposs DiseaseAnabolismAnimalsApplications GrantsBehaviorBehavioralBehavioral AssayBiochemicalBioinformaticsBiological AssayBrainBrain regionCollaborationsCorpus striatum structureDevelopmentDiseaseDrug AddictionEndocrineEndopeptidasesEnzymesExhibitsFamilyGenerationsHealthHippocampus (Brain)Homology ModelingIllinoisImmuneKnock-outKnowledgeLabelLearningMass Spectrum AnalysisMemoryMetalloproteasesModelingMolecular ModelsMusNatureNeprilysinNeurodegenerative DisordersNeuronsNeuropeptidesNeurosecretory SystemsPathologyPathway interactionsPeptide HydrolasesPeptidesPhenotypeProcessProductionPropertyProtein PrecursorsProteinsProteolysisProteolytic ProcessingPublicationsRegulationRoleSiteStructureStudy SectionSubtilisinsTechnologyTestingTissuesUniversitiesWild Type Mousebasedrug of abuseendothelin converting enzyme-2in vivoinsightinterdisciplinary approachmembermolecular modelingmutantnovelnovel therapeuticsresponsetreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A wide variety of proteins in neuronal, endocrine and immune tissues undergo proteolytic processing. Many of these proteins and peptides are intercellular messengers. Most neuroendocrine peptides are synthesized from precursor proteins. Post-translational processing of these precursors is a key step in the production of biologically active peptides. In the majority of cases this occurs by proteolysis of the precursors at 'classical' cleavage sites involving endopeptidases of the subtilisin family. A subset of bioactive peptides are generated by processing at 'non-classical' cleavage sites; the protease(s) responsible for these cleavages have not been well explored. Members of the metalloendoprotease family are thought to be involved in non- classical processing. Among them, endothelin converting enzyme-2 (ECE-2) is a good candidate since it exhibits functional properties that are consistent with it being a neuropeptide biosynthetic enzyme. In this grant application we propose to examine the hypothesis that "ECE-2 is neuropeptide processing enzyme that generates novel bioactive peptides by non-classical processing". The specific aims are, (i) to characterize the biochemical and enzymological properties of ECE-2, (ii) to study the behavioral phenotype of animals lacking ECE-2 including addictive behaviors, and (iii) to examine the peptide profile in mice lacking ECE-2 using differential isotopic labeling and mass spectrometry. These studies are synergistic and will expand our current knowledge of neuropeptide processing by providing information about novel neuropeptides. Furthermore, findings from these studies will form a basis for future research exploring the functions of these novel neuropeptides in vivo. Since a variety of neuropeptides are involved in normal functioning of the brain, understanding the mechanisms that regulate their endogenous levels becomes a prerequisite to the development of strategies for the treatment of a variety of pathologies including neurodegenerative disorders and drug addiction. PUBLIC HEALTH RELEVANCE: This proposal describes studies on endothelin converting enzyme-2 - a peptide processing enzyme shown to be involved in a number of disorders including drug addiction and Alzheimer's disease. The findings from the proposed studies would help in the development of novel therapeutics for the treatment of these and other neuroendocrine disorders.
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