Fluorescent aptasensor based on conformational switch–induced hybridization for facile detection of β-amyloid oligomers
- 30 September 2022
- journal article
- research article
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 414 (28) , 8155-8165
Abstract
Aβ oligomers (AβO) are a dominant biomarker for early Alzheimer’s disease diagnosis. A fluorescent aptasensor coupled with conformational switch–induced hybridization was established to detect AβO. The fluorescent aptasensor is based on the interaction of fluorophore-labeled AβO-specific aptamer (FAM-Apt) against its partly complementary DNA sequence on the surface of magnetic beads (cDNA-MBs). Once the FAM-Apt binds to AβO, the conformational switch of FAM-Apt increases the tendency to be captured by cDNA-MBs. This causes a descending fluorescence of supernatant, which can be utilized to determine the levels of AβO. Thus, the base-pair matching above 12 between FAM-Apt and cDNA-MBs with increasing hybridizing free energies reached the ascending fluorescent signal equilibrium. The optimized aptasensor showed linearity from 1.7 ng mL−1 to 85.1 (R = 0.9977) with good recoveries (79.27–109.17%) in plasma. Furthermore, the established aptasensor possesses rational selectivity in the presence of monomeric Aβ, fibrotic Aβ, and interferences. Therefore, the developed aptasensor is capable of quantifying AβO in human plasma and possesses the potential to apply in clinical cases. Graphical AbstractKeywords
This publication has 44 references indexed in Scilit:
- Ammonium hydroxide treatment of Aβ produces an aggregate free solution suitable for biophysical and cell culture characterizationPeerJ, 2013
- Selection of DNA Aptamers That Recognize α-Synuclein Oligomers Using a Competitive Screening MethodAnalytical Chemistry, 2012
- Methods for the determination of limit of detection and limit of quantitation of the analytical methodsChronicles of Young Scientists, 2011
- Aβ40 Oligomers Identified as a Potential Biomarker for the Diagnosis of Alzheimer's DiseasePLOS ONE, 2010
- Preparation and characterization of toxic Aβ aggregates for structural and functional studies in Alzheimer's disease researchNature Protocols, 2010
- RAGE (Yin) Versus LRP (Yang) Balance Regulates Alzheimer Amyloid β-Peptide Clearance Through Transport Across the Blood–Brain BarrierStroke, 2004
- Common Structure of Soluble Amyloid Oligomers Implies Common Mechanism of PathogenesisScience, 2003
- An improved method of preparing the amyloid β-protein for fibrillogenesis and neurotoxicity experimentsAmyloid, 2000
- In vitro selection of RNA molecules that bind specific ligandsNature, 1990
- Systematic Evolution of Ligands by Exponential Enrichment: RNA Ligands to Bacteriophage T4 DNA PolymeraseScience, 1990