Small, modular, and monovalent Quantum Dots for single molecule imaging of Notch
Small, modular, and monovalent Quantum Dots for single molecule imaging of Notch
批准号:
8811423
负责人:
Zev Jordan Gartner
金额:
$18.7万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-03-01 至 2016-02-29
关键词:
AddressAffectAffinityBedsBindingBiologicalBiologyBioprobeBiotinCell Culture TechniquesCell Surface ProteinsCell physiologyCell surfaceCellsChemistryCritical PathwaysDNADevelopmentDiagnosticDiffusionDisciplineDiseaseEnzyme-Linked Immunosorbent AssayEventExclusionFluorescent DyesFutureGoalsHealthImageIn VitroLabelLeadLifeLymphomaMalignant NeoplasmsMapsMembrane ProteinsMethodsModificationMolecularMorphologic artifactsMultiple SclerosisNoiseOligonucleotidesOpticsPerformancePoisson DistributionPolymersPolysaccharidesProcessPropertyProteinsQuantum DotsReactionReagentResolutionS-nitro-N-acetylpenicillamineScientistSignal TransductionSpecificityStreptavidinSurfaceTestingTherapeuticTimeWestern Blottingbasebioimagingdesignfluorescence imagingfluorophoreimaging agentimaging probeimprovedinnovationinterfacialmolecular imagingmonomernanoparticlenotch proteinpreventprogramsprotein structurereceptorsingle moleculespatiotemporaltool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Quantum dots have the potential to revolutionize biological imaging due to their exceptional photophysical properties. However, precise control over the interfacial chemistry between QDs and other biomolecules remains a significant synthetic challenge limiting their broad application in biology. Common strategies for preparing QD-biomolecule conjugates generate products with poorly defined valency, relatively large hydrodynamic size, and limited modularity. To address these issues and hence to establish higher-performance and more versatile QD imaging probes, we propose an innovative synthetic approach, termed "steric exclusion". The method uses a functionalized steric-exclusion oligonucleotide designed to wrap the QD as it reacts and thereby limits the extent of the reaction to a species of fixed valency. We propose to (i) perform the single-step complete conversion of QDs to bioimaging probes that are small (< 12 nm), modular, highly-specific, and monovalent; and (ii) demonstrate the utility of these probes in a challenging single- molecule imaging application by elucidating the dynamics of Notch and its processing intermediates on the surface of live cells. Ultimately, we propose to transform QDs from "probes for special purposes" to "versatile and ready-to-use bioprobes," accessible to scientists from any discipline.
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