Enzymes involved in neuropeptide biosynthesis and regulation
Enzymes involved in neuropeptide biosynthesis and regulation
批准号:
8456161
负责人:
Lakshmi A Devi
金额:
$34.21万
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 AddictionEndocrineEndopeptidasesEnzymesExhibitsFamilyGenerationsHippocampus (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
神经元、内分泌和免疫组织中的多种蛋白质经历蛋白水解加工。
这些蛋白质和肽中的许多是细胞间信使。大多数神经内分泌肽
由前体蛋白质合成。这些前体的翻译后加工是转录过程中的关键步骤。
生物活性肽的生产。在大多数情况下,这是通过前体的蛋白水解发生的。
在涉及枯草杆菌蛋白酶家族的内肽酶的“经典”切割位点。生物活性肽的一个子集是
通过在“非经典”切割位点加工产生;负责这些切割的蛋白酶
还没有得到很好的探索。金属内切蛋白酶家族的成员被认为参与非-
经典处理其中,内皮素转换酶-2(ECE-2)是一个很好的候选者,因为它
表现出与其作为神经肽生物合成酶一致的功能特性。在这份赠款中,
应用我们提出检验“ECE-2是神经肽加工酶,
通过非经典加工产生新的生物活性肽”。
具体目标是,(i)表征ECE-2的生化和酶学性质,(ii)
研究缺乏ECE-2的动物的行为表型,包括成瘾行为,以及(iii)检查
使用差异同位素标记和质谱法在缺乏ECE-2的小鼠中的肽谱。
这些研究是协同作用的,将通过以下方式扩展我们目前对神经肽加工的知识:
提供关于新的神经肽的信息。此外,这些研究的结果将成为
未来的研究探索这些新的神经肽在体内的功能。由于各种神经肽
参与大脑的正常功能,了解调节其内源性的机制,
水平成为发展各种病理学治疗策略的先决条件
包括神经退行性疾病和药物成瘾。
英文摘要
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.
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