HRP cDNA expression: a label for modern electron microscopy on neuroscience
HRP cDNA expression: a label for modern electron microscopy on neuroscience
批准号:
7845476
负责人:
THOMAS SCHIKORSKI
金额:
$14.8万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-01 至 2012-05-31
关键词:
Adenovirus VectorAreaAxonBiological PreservationBiological ProcessBiologyBrainCellular biologyChimera organismCommunitiesComplementary DNADevelopmentDockingElectron MicroscopeElectron MicroscopyElectronsEngineeringGenesGeneticGenetic MarkersGreen Fluorescent ProteinsHistocytochemistryHorseradish PeroxidaseKnowledgeLabelLifeLinkMicroscopicMolecular StructureMotivationMusNeurobiologyNeuronsNeurosciencesProceduresPropertyProteinsPyramidal CellsReporter GenesResearchResearch PersonnelResolutionSiteStaining methodStainsStructureStructure-Activity RelationshipSynapsesSynaptic VesiclesSystemTechniquesTransgenic AnimalsTransgenic MicecDNA Expressioncell typecellular imagingelectron tomographyhippocampal pyramidal neuroninsightinterestmutantneocorticalpresynapticpromoterreconstructionsynaptic functiontool
中文摘要
描述(由研究者提供):大分子结构的组织是
我们对蛋白质性质和生物学功能的理解中缺失的一环。需要找到
因此,生物功能和大分子结构之间的详细关系是无可争议的
在几乎所有生物学领域。绿色荧光蛋白(GFP)的引入使其成为可能
在细胞水平上研究结构与功能的关系,并开始了细胞生物学的革命。
然而,只有电子显微镜(EM)提供足够的分辨率来研究的组织,
大分子结构,以及EM报告基因的缺乏阻碍了遗传方法
几十年来一直致力于精细结构研究最近,我们将辣根过氧化物酶(HRP)cDNA
作为一种遗传标记,可以标记整个神经元,而不会破坏精细结构。这个标记,
与现代EM方法(例如,高分辨率电子层析成像),具有很大潜力
通过扩大我们对神经科学和细胞生物学的了解,
大分子组织
英文摘要
DESCRIPTION (provided by investigator): The organization of macromolecular structures is the
missing link in our understanding of the properties of proteins and biological function. The need to find
the detailed relationship between biological function and macromolecular structure is, thus, undisputed
in almost all areas of biology. The introduction of green fluorescent protein (GFP) has made it possible
to study structure-function relationships at the cellular level and started a revolution in cell biology.
However, only electron microscopy (EM) provides sufficient resolution to study the organization of
macromolecular structures, and the lack of a reporter gene for EM has hampered genetic approaches
in fine structural research for decades. Recently, we introduced horseradish peroxidase (HRP) cDNA
as a genetic marker that can label entire neurons without destroying the fine structure. This marker,
together with modern EM approaches (e.g., high resolution electron tomography), has a great potential
to advance the field of neuroscience and all areas of cell biology by expanding our knowledge of
macromolecular organization.
期刊论文(1)
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科研奖励(0)
会议论文
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