Multi-Channel Sensing using Fluorescent Protein-Nanoparticle Sensors
Multi-Channel Sensing using Fluorescent Protein-Nanoparticle Sensors
批准号:
8446462
负责人:
VINCENT M. ROTELLO
金额:
$28.32万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-03-08 至 2015-03-31
关键词:
BacteriaBuffersCancerousCell Culture TechniquesCell LineCell Surface ProteinsCell surfaceCellsChemicalsChemistryComplexComplex MixturesCultured CellsDetectionDiseaseElementsEngineeringFluorescenceGenerationsGoalsGoldHumanImageryIndividualMicrofluidicsModelingNP proteinNoseOligopeptidesPatternPlant ResinsPolymersPorphyrinsProteinsResearchResponse to stimulus physiologySerumSurfaceSystemTechniquesTechnologyTissue StainsTissuesTonguebasecell typedesignexpectationexperiencefluorophoreimprovedmalignant breast neoplasmnanoparticlenovel diagnosticsparticleprogramspublic health relevancerapid techniqueratiometricreceptorsensortool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The "chemical nose/tongue" approach presents a potential alternative to specific recognition and separations techniques. In this approach a sensor array is generated to provide differential interaction with analytes via selective receptors, generating a stimulus response pattern that can be statistically analyzed and used for the identification of individual target analytes and also analysis of complex mixtures. Recently, we have developed nanoparticle-fluorescent polymer sensors for identification of proteins, bacteria, and cancerous cells through a fluorophore-displacement mechanism as well as a highly sensitive nanoparticle-GFP based "chemical nose" strategy for protein detection in biofluid. Current chemical nose sensors for proteins and cell-surfaces are single channel, meaning a separate well or channel is required for each sensing element. This requirement for spatially distinct sensor elements complicates both microplate-based techniques and the application of array-based sensing in other venues, including microfluidics platforms and tissue staining. To overcome this limitation, we will exploit the spectral range of fluorescent proteins (FPs) to provide multi-channel fluorescence transduction for sensing applications. Multi-channel sensing will facilitate implementation of array-based sensing, allowing "one well" sensing while improving sensitivity through generation of ratiometric dadt. In this program, we will use the tools of supramolecular chemistry to synergistically engineer both the protein and AuNP quencher to provide highly efficient and versatile platforms for protein and cell surface sensing.
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