Optical Microscopy Core
Optical Microscopy Core
批准号:
7760767
负责人:
MARK A. MC NIVEN
金额:
$23.15万
依托单位:
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:
2009-09-01 至 2014-08-31
关键词:
ArtsBioprobeCellsCollectionComputersConfocal MicroscopyCoupledDataDevelopmentDoctor of PhilosophyEpithelialEquipmentFacultyFluorescenceFluorescence Recovery After PhotobleachingFluorescence Resonance Energy TransferGastroenterologyGoalsGreen Fluorescent ProteinsHepatologyHuman ResourcesImageImaging technologyIndividualInstructionLifeLipidsLiverMeasuresMethodsMicroscopicMicroscopyMorphologyNeuronsOpticsPancreasPhysiologicalPlayProteinsPublishingReportingResearchResearch InfrastructureResearch PersonnelResolutionResourcesRoleSignal PathwaySignal TransductionSignaling MoleculeTechnologyThree-Dimensional ImageTimeTissuesTrainingbasecellular imagingimage reconstructionimaging modalityinnovationmeetingsmembernoveloptical imagingprogramsprotein protein interactionresponsetool
中文摘要
光学形态核心将在支持中心的总体目标方面发挥重要作用。
这个核心的具体目标有三个方面。第一,提供可靠、可访问和最先进的
向所有中心成员提供微观技术,促进他们对G1细胞信号的研究
瀑布。第二,教育和培训中心成员使用基本的和复杂的
细胞成像方法。重点将放在提供技术指导以及
教育教职员工这种方法如何扩大他们的科学研究的范围和广度
程序。第三,最先进的光学成像技术在全球范围内的发展和应用
组织/细胞,包括:活细胞的高分辨率实时计算机/视频成像;共聚焦
显微结合计算机三维图像重建;荧光共振能
用于测量动态蛋白质相互作用的转移(FRET)应用;荧光恢复
光漂白后(FRAP),可以定量测定蛋白质的募集/周转;表达
以及促进特定信号的研究和定位的基于荧光的生物探针的使用
包括蛋白质和脂类在内的分子,以及特定的光激活物质的开发和应用
笼状化合物,允许精确的时间和空间激活所需的信号
活细胞中的分子。
英文摘要
The Optical Morphology Core will play an essential role in supporting the overall goals of the Center.
The Specific Aims of this core are three-fold. First, to provide reliable, accessible, and state-of-the-art
microscopic technology to all Center members that will facilitate their study of Gl cellular signaling
cascades. Second, to educate and train Center members in the use of both basic and sophisticated
cellular imaging methods. Emphasis will be placed on providing technical instruction as well as
educating faculty about how such approaches can expand the scope and breadth of their scientific
programs. Third, development and application of state-of-the-art optical imaging technologies to Gl
tissues/cells including; high resolution, real-time computer/video imaging of live cells; confocal
microscopy coupled with computer-based 3-D image reconstruction; Fluorescence Resonance Energy
Transfer (FRET) applications to measure dynamic protein-protein interactions; Fluorescence Recovery
After Photobleaching (FRAP) that allows the quantitation of protein recruitment/turnover; expression
and use of fluorescence-based bioprobes that facilitates the study and localization of specific signaling
molecules including both proteins and lipids; and the development and application of specific photoactivatable
caged-compounds that allow a precise temporal and spatial activation of desired signaling
molecules in live cells.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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