{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sharma B"],"funding":["Clemson University","NIEHS NIH HHS","National Institutes of Health"],"pagination":["14010-14015"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7085113"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(29)"],"pubmed_abstract":["Here, we present a graphene-based analyte-induced disruption of luminescence quenching (AIDLuQ) assay for specific detection of biomarkers with femtomolar sensitivity. In the AIDLuQ assay, antibody (Ab)-conjugated quantum dots (QDs) are initially deposited on graphene-coated paper. However, the emission from QDs is quenched due to resonance energy transfer to graphene. Upon the addition of an analyte (An) corresponding to Ab, the QDs-Ab-An complex is lifted above the surface resulting in the disruption of the quenching from graphene and the recovery of the luminescence of the QDs. The percentage of recovery depends upon the concentration of the analyte, allowing one to create standard curves for effective quantification. Despite its rapidity in assay time (15-20 min), the graphene platform"],"journal":["Nanoscale"],"pubmed_title":["Analyte-induced disruption of luminescence quenching (AIDLuQ) for femtomolar detection of biomarkers."],"pmcid":["PMC7085113"],"funding_grant_id":["R01 ES019311","R01ES019311-07"],"pubmed_authors":["Sharma B","Chiluwal S","Podila R"],"additional_accession":[]},"is_claimable":false,"name":"Analyte-induced disruption of luminescence quenching (AIDLuQ) for femtomolar detection of biomarkers.","description":"Here, we present a graphene-based analyte-induced disruption of luminescence quenching (AIDLuQ) assay for specific detection of biomarkers with femtomolar sensitivity. In the AIDLuQ assay, antibody (Ab)-conjugated quantum dots (QDs) are initially deposited on graphene-coated paper. However, the emission from QDs is quenched due to resonance energy transfer to graphene. Upon the addition of an analyte (An) corresponding to Ab, the QDs-Ab-An complex is lifted above the surface resulting in the disruption of the quenching from graphene and the recovery of the luminescence of the QDs. The percentage of recovery depends upon the concentration of the analyte, allowing one to create standard curves for effective quantification. Despite its rapidity in assay time (15-20 min), the graphene platform","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Aug","modification":"2025-06-01T12:01:17.093Z","creation":"2020-09-11T07:24:50Z"},"accession":"S-EPMC7085113","cross_references":{"pubmed":["31309963"],"doi":["10.1039/c9nr04308j"]}}