Novel single-stranded DNA binding protein-assisted fluorescence aptamer switch based on FRET for homogeneous detection of antibiotics

التفاصيل البيبلوغرافية
العنوان: Novel single-stranded DNA binding protein-assisted fluorescence aptamer switch based on FRET for homogeneous detection of antibiotics
المؤلفون: You Zhou, Ye Wang, Tianhua Li, Yinji Chen, Yuting Cao, Ning Gan
المصدر: Biosensorsbioelectronics. 87
سنة النشر: 2016
مصطلحات موضوعية: Analyte, Aptamer, Biomedical Engineering, Biophysics, Analytical chemistry, Metal Nanoparticles, 02 engineering and technology, Biosensing Techniques, 01 natural sciences, Limit of Detection, Quantum Dots, Electrochemistry, Fluorescence Resonance Energy Transfer, Animals, Single-strand DNA-binding protein, Quenching (fluorescence), Chemistry, 010401 analytical chemistry, General Medicine, Aptamers, Nucleotide, 021001 nanoscience & nanotechnology, Fluorescence, 0104 chemical sciences, Anti-Bacterial Agents, DNA-Binding Proteins, Förster resonance energy transfer, Chloramphenicol, Milk, Quantum dot, Colloidal gold, Gold, 0210 nano-technology, Biotechnology
الوصف: Herein, a smart single-stranded DNA binding protein (SSB)-assisted fluorescence aptamer switch based on fluorescence resonance energy transfer (FRET) was designed. The FRET switch was synthesized by connecting SSB labeled quantum dots (QDs@SSB) as donor with aptamer (apt) labeled gold nanoparticles (AuNPs@apt) as acceptor, and it was employed for detecting chloramphenicol (CAP) in a homogenous solution. In the assay, the interaction between core-shell QDs@SSB and AuNPs@apt leads to a dramatic quenching (turning off). After adding CAP in the detection system, AuNPs@apt can bind the target specifically then separate QDs@SSB with AuNPs@apt-target, resulting in restoring the fluorescence intensity of QDs (turning on). Consequently, the fluorescence intensity recovers and the recovery extent can be used for detection of CAP in homogenous phase via optical responses. Under optimal conditions, the fluorescence intensity increased linearly with increasing concentrations of CAP from 0.005 to 100ngmL-1. The limit of this fluorescence aptamer switch was around 3pgmL-1 for CAP detection. When the analyte is changed, the assay can be applied to detect other targets only by changing relative aptamer in AuNPs@apt probe. Furthermore, it has potential to be served as a simple, sensitive and portable platform for antibiotic contaminants detection in biological and environmental samples.
تدمد: 1873-4235
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03ee32ac5252cef9681de124695346eaTest
https://pubmed.ncbi.nlm.nih.gov/27596250Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....03ee32ac5252cef9681de124695346ea
قاعدة البيانات: OpenAIRE