Analytical Chemistry · 2024 · 29 citations · 30 references
Natural SciencesChemistryMolecular BiologyAnalytical ChemistryBiosensorsMolecular DiagnosticsCancer Molecular DiagnosticsChemical SensorsCirculating Tumor Dna AnalysisLanthanide ChemistryLiquid BiopsyMolecular SensorsCirculating Tumor Dna DetectionCirculating Tumor Dna TestingFluorescence QuantificationFluorescence SensingHost-guest InteractionsLanthanide Bioinorganic ChemistryLanthanide ChelationLiquid Biopsy Detection
Detection of circulating tumor DNA (ctDNA) in liquid biopsy is of great importance for tumor diagnosis but difficult due to its low amount in bodily fluids. Herein, a novel ctDNA detection platform is established by quantifying DNA amplification by-product pyrophosphate (PPi) using a newly designed bivariable lanthanide metal–organic framework (Ln-MOF), namely, Ce/Eu-DPA MOF (CE-24, DPA = pyridine-2,6-dicarboxylic acid). CE-24 MOF exhibits ultrafast dual-response (fluorescence enhancement and enzyme-activity inhibition) to PPi stimuli by virtue of host–guest interaction. The platform is applied to detecting colon carcinoma-related ctDNA (KARS G12D mutation) combined with the isothermal nucleic acid exponential amplification reaction (EXPAR). ctDNA triggers the generation of a large amount of PPi, and the ctDNA quantification is achieved through the ratio fluorescence/colorimetric dual-mode assay of PPi. The combination of the EXPAR and the dual-mode PPi sensing allows the ctDNA assay method to be low-cost, convenient, bioreaction-compatible (freedom from the interference of bioreaction systems), sensitive (limit of detection down to 10 1 fM), and suitable for on-site detection. To the best of our knowledge, this work is the first application of Ln-MOF for ctDNA detection, and it provides a novel universal strategy for the rapid detection of nucleic acid biomarkers in point-of-care scenarios.
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