Biomimetic Chip Enhanced Time-Gated Luminescent CRISPR-Cas12a Biosensors under Functional DNA Regulation.
Cheng-Yu LiBei ZhengLi-Li LuWen-Kai FangMing-Qiu ZhengJia-Ling GaoLiu YuhengDai-Wen PangHong-Wu TangPublished in: Analytical chemistry (2021)
Despite that the currently discovered CRISPR-Cas12a system is beneficial for improving the detection accuracy and design flexibility of luminescent biosensors, there are still challenges to extend target species and strengthen adaptability in complicated biological media. To conquer these obstacles, we present here some useful strategies. For the former, the limitation to nucleic acids assay is broken through by introducing a simple functional DNA regulation pathway to activate the unique trans-cleavage effect of this CRISPR system, under which the expected biosensors are capable of effectively transducing a protein (employing dual aptamers) and a metal ion (employing DNAzyme). For the latter, a time-gated luminescence resonance energy transfer imaging manner using a long-persistent nanophosphor as the energy donor is performed to completely eliminate the background interference and a nature-inspired biomimetic periodic chip constructed by photonic crystals is further combined to enhance the persistent luminescence. In line with the above efforts, the improved CRISPR-Cas12a luminescent biosensor not only exhibits a sound analysis performance toward the model targets (carcinoembryonic antigen and Na+) but also owns a strong anti-interference feature to actualize accurate sensing in human plasma samples, offering a new and applicative analytical tool for laboratory medicine.
Keyphrases
- energy transfer
- crispr cas
- label free
- genome editing
- quantum dots
- high throughput
- circulating tumor
- circulating tumor cells
- high resolution
- cell free
- single molecule
- nucleic acid
- sensitive detection
- machine learning
- wastewater treatment
- gold nanoparticles
- living cells
- deep learning
- protein protein
- genome wide
- dna methylation
- tissue engineering
- data analysis
- small molecule
- liquid chromatography
- high speed
- transcription factor