Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
批准号:
8112653
负责人:
TOM KLAUS KERPPOLA
金额:
$67.03万
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:
2008-09-30 至 2014-07-31
关键词:
AddressAnimalsBacteriaBindingBiological AssayCell physiologyCellsCharacteristicsChromatinChromatin LoopCommitComplexDNADetectionDevelopmentElementsEnergy TransferEnsureEventEvolutionFluorescenceFrequenciesGenesGenetic RecombinationGenetic TranscriptionHealthImageImageryImmunoglobulin GenesImmunoglobulinsIn VitroIndividualLaboratoriesLifeLightLinkLymphocyteMacromolecular ComplexesMediatingMethodsMicroscopyMolecularNuclearNucleic Acid Regulatory SequencesNucleoproteinsOrganismPerformancePlant GenomePlantsPrincipal InvestigatorProtein FragmentProteinsResearchResolutionSignal TransductionSiteSystemT-DNAUbiquitinWorkbasecellular imagingchemical synthesisdesignimage processingimaging modalityimaging probeimprovedmolecular imagingmolecular scalenovelpathogenpublic health relevancescaffold
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A major objective of high resolution imaging of cells is to visualize the molecular organization of cellular components and to determine if specific components participate in the same macromolecular complex. Efforts to address these issues have tackled the problem from two opposite perspectives: 1. Improvements in microscopy have enabled resolution of spectrally distinct signals at a molecular scale under ideal conditions; and 2. Energy transfer approaches have allowed detection of complexes where two proteins are in very close contact. This proposal introduces a third approach that fills the gap in resolution between the two former methods and avoids many of the compromises inherent in them. This approach is based on formation of a fluorescent complex when the association between two non-fluorescent protein fragments is facilitated by tethering the fragments in a macromolecular complex. Earlier adaptations of this approach are known as bimolecular fluorescence complementation (BiFC) and ubiquitin-mediated fluorescence complementation (UbFC). These earlier approaches have significant limitations that are due to the lack of optimization of the fluorescent protein fragments (BiFC probes) for purposes of the assay. The proposed research seeks to eliminate these limitations through systematic in vitro evolution and protein design strategies. The research team will develop novel BiFC probes that will enable imaging of cellular processes that have not been previously imaged due to limitations inherent in existing methods. To validate the universal utility of the BiFC probes, they will be used to image molecular events involving bacteria, plants and animal cells. Public Health Relevance: Many cellular functions require that multiple components come together to form a complex. We propose to develop new methods that will enable us to see the complexes formed by specific combinations of components. These methods are analogous to linking a light bulb to one component and a battery to the other. This work will improve our understanding of interactions among cellular components that are important for the health of the cell and the organism.
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DOI:
10.1016/j.jmb.2009.08.069
发表时间:
2009-12-04
期刊:
Journal of molecular biology
影响因子:
5.6
作者:
[Robida AM, Kerppola TK]
通讯作者:
Kerppola TK
DOI:
10.1039/b909638h
发表时间:
2009-10
期刊:
Chemical Society reviews
影响因子:
46.2
作者:
[Kerppola TK]
通讯作者:
Kerppola TK
DOI:
10.1038/nri3570
发表时间:
2014-02
期刊:
Nature reviews. Immunology
影响因子:
--
作者:
[]
通讯作者:
DOI:
10.1016/bs.mie.2017.02.003
发表时间:
2017
期刊:
Methods in enzymology
影响因子:
--
作者:
[Deng H, Kerppola TK]
通讯作者:
Kerppola TK
DOI:
10.1016/j.tcb.2009.10.001
发表时间:
2009-12
期刊:
TRENDS IN CELL BIOLOGY
影响因子:
19
作者:
[Kerppola, Tom K.]
通讯作者:
Kerppola, Tom K.
共 6 条
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
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批准号:8268442
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项目类别:
-
资助金额:$34.4万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
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批准号:8491945
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项目类别:
-
资助金额:$0.7万
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财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
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依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
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批准号:8139012
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项目类别:
-
资助金额:$34.4万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
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批准号:8490698
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项目类别:
-
资助金额:$33.36万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
-
批准号:8849059
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项目类别:
-
资助金额:$0.44万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
-
批准号:9271347
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项目类别:
-
资助金额:$0.85万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using Fl
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批准号:8663854
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项目类别:
-
资助金额:$34.4万
-
财政年份:2010
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
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批准号:7924978
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项目类别:
-
资助金额:$11.59万
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财政年份:2009
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
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批准号:7556679
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项目类别:
-
资助金额:$67.93万
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财政年份:2008
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
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批准号:7694976
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项目类别:
-
资助金额:$66.66万
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财政年份:2008
-
负责人:TOM KLAUS KERPPOLA
-
依托单位:
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging F
-
批准号:7907625
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项目类别:
-
资助金额:$67.84万
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财政年份:2008
-
负责人:TOM KLAUS KERPPOLA
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依托单位:
海外基金