Rapid SARS-CoV-2 Detection Using Amplicon Templated Reporter Enzyme Assembly
Rapid SARS-CoV-2 Detection Using Amplicon Templated Reporter Enzyme Assembly
批准号:
10438883
负责人:
Brian Patrick Callahan
金额:
$7.85万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-07-01 至 2024-06-30
关键词:
2019-nCoVAgreementAwardBase PairingBiological AssayBiosensorBuffersCOVID-19COVID-19 assayCOVID-19 detectionCOVID-19 diagnosisCOVID-19 pandemicCOVID-19 testCOVID-19 testingCessation of lifeClinicalComplementConsumptionDNADiagnosticEngineeringEnzymatic BiochemistryEnzymesEventExonucleaseFundingGenetic Complementation TestGoalsInfectionLaboratoriesLegal patentLightLuciferasesMethodsMolecularMolecular GeneticsNASBA AnalysisNucleic AcidsOligonucleotide ProbesOligonucleotidesOutputProtein FragmentProteinsPublishingRNARNA amplificationReadingReporterReportingResearch PersonnelSARS-CoV-2 infectionSamplingSensitivity and SpecificitySignal TransductionSpecificitySpeedSystemTechniquesTechnologyTest ResultTestingTimebasecomplement systemdesigndetection limitdiagnostic platformexperimental studyimprovedinnovationisothermal amplificationluminescencemolecular assembly/self assemblynovelpathogenpilot testprotein protein interactionreconstitutiontool
中文摘要
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英文摘要
ABSTRACT
We are proposing to pilot test a new enzyme biosensor technology for the purpose of enhancing
isothermal RNA amplification assays for SARS-CoV-2. Our overarching goal is to validate this
technology, called DETECT, as biomolecular tool to increase the sensitivity, specificity, and
speed of SARS-CoV-2 testing. DETECT is based on a modified split luciferase enzyme
complementation assay. Instead of the standard bait and prey fused protein constructs, we
connect two non-interacting luciferase fragments to SARS-CoV-2 oligonucleotide probes.
Conjugation of the luciferase fragments to the oligonucleotides uses a chemi-enzymatic method
developed in the investigator's lab. The oligonucleotides are designed to anneal to adjacent
segments in a unique SARS-CoV-2 amplicon. With samples containing the amplicon, the split
luciferase fragments are brought together through base pairing of their attached
oligonucleotides with the SARS-CoV-2 amplicon. Molecular assembly reconstitutes functional
luciferase from the two fragments, enabling robust light output. In preliminary experiments, we
validate the central and novel concept of DETECT: protein fragment complementation via
nucleic acid base pairing. In controls where base pairing of the oligonucleotides is blocked,
either by exonuclease pretreatment or by competitor oligonucleotide, we observe luminescence
readings on par with buffer only samples. By contrast, in experimental samples where
oligonucleotide base pairing is supported, we observe luciferase signal that is increased 100-
fold over background. These preliminary experiments were carried out with the split luciferase-
oligonucleotide conjugates at 25 nM. Over the course of this 2-year project, we propose to
evaluate the DETECT system quantitatively for specificity, sensitivity and speed, thereby
assessing the clinical potential of this biosensor technology. Although our objective here is
diagnosing SARS-CoV-2 infection, the DETECT system is easily re-programmed by changing
the oligonucleotide probe sequences. Thus DETECT holds promise as a new and innovative
diagnostic platform.
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Rapid SARS-CoV-2 Detection Using Amplicon Templated Reporter Enzyme Assembly
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批准号:10289105
-
项目类别:
-
资助金额:$7.85万
-
财政年份:2021
-
负责人:Brian Patrick Callahan
-
依托单位:
Structural Mechanisms of Hedgehog Autoprocessing in Physiology and Disease
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批准号:10063481
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项目类别:
-
资助金额:$43.35万
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财政年份:2016
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负责人:Brian Patrick Callahan
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依托单位:
NCI Diversity Fellowship
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批准号:9902835
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项目类别:
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资助金额:$3.73万
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财政年份:2016
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负责人:Brian Patrick Callahan
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依托单位:
海外基金