Simplified Single Molecule Protein Assays with Unprecedented Sensitivity
Simplified Single Molecule Protein Assays with Unprecedented Sensitivity
批准号:
10657044
负责人:
DAVID R. WALT
金额:
$12.8万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-05-05 至 2027-04-30
关键词:
AbbreviationsAddressAntibodiesAntigensBacterial AntigensBar CodesBindingBiologicalBiological AssayBiological MarkersBiological ProcessBiosensing TechniquesBloodClassificationClinicalClinical SensitivityComplexDNA amplificationDataDetectionDevicesDiagnosisDiagnostic SpecificityDiseaseEngineeringEnvironmentEnzyme-Linked Immunosorbent AssayEnzymesEventFilmFingersFluorescent DyesFluorescent ProbesFoodFoundationsFutureGenerationsHuman ResourcesImageIndividualInfrastructureLabelLaboratoriesLicensingLiquid substanceMeasurementMeasuresMethodsMicroscopeModelingMolecularMonitorMycobacterium tuberculosis antigensNeurodegenerative DisordersPathogen detectionPatientsPerformancePlayProtein AnalysisProteinsResearchResource-limited settingRoleSalivaSamplingSchemeSignal TransductionSlideTechniquesTechnologyTestingTimeToxinTrainingTranslatingTriageTuberculosisUrineViral AntigensWorkantigen detectioncancer biomarkersclinical applicationclinically actionablecommercializationcostcross reactivitydetection limitdiagnostic platformdiagnostic valuedigitalimprovedinstrumentinstrumentationlipoarabinomannanmonolayermultiplex assaymultiplex detectionpoint of careprotein biomarkerssealsingle moleculeurinary
中文摘要
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英文摘要
PROJECT SUMMARY
The ability to measure extremely low levels of biomolecules accurately and rapidly is essential for diagnosing
and monitoring many diseases. While sufficient for certain biomarkers, the sensitivities of most existing
diagnostic systems are inadequate for measuring many protein biomarkers that exist in easily accessible
biofluids at concentrations below the picomolar range. In this application, we propose to engineer and refine a
new ultrasensitive single molecule protein analysis platform that will be able to routinely measure attomolar
protein concentrations, which we call Molecular On-bead Signal Amplification for Individual Counting (MOSAIC).
MOSAIC transforms single molecule measurements into a simplified assay format via on-bead signal
localization, which has the potential to be integrated into a point of care (POC) device. In MOSAIC, a non-
diffusible signal is generated on each bead carrying a target molecule, creating an on-bead signal that remains
attached for prolonged periods of time, thereby enabling alternative detection schemes to be employed that do
not require bead confinement into microwells or droplets to localize signals. A key challenge to be addressed in
the proposed work will be to ensure that this MOSAIC platform can consistently outperform current ultrasensitive
protein detection technologies in sensitivity by one to two orders of magnitude across many protein analytes,
which in turn lays the foundation for future work in translating this enhanced analytical sensitivity to improved
clinical sensitivity and specificity for diagnostic applications. In Aims 1 and 2, we will optimize signal generation
and readout methods for MOSAIC and expand its multiplexing capabilities. In Aim 3, we will evaluate the
diagnostic utility of MOSAIC in a proof-of-principle clinical application to detect very low abundance
Mycobacterium tuberculosis antigens in urine as a potential triage test for tuberculosis. The resulting biosensing
technology will provide an ultrasensitive diagnostic platform that will open up protein analysis to previously
inaccessible biomarkers and also be readily and affordably utilized across both research and clinical laboratories
using common laboratory instruments.
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Simplified Single Molecule Protein Assays with Unprecedented Sensitivity
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海外基金