Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout.
Lauren M AufdembrinkPavana KhanNathaniel J GautKatarzyna P AdamalaAaron E EngelhartPublished in: RNA (New York, N.Y.) (2020)
Isothermal, cell-free, synthetic biology-based approaches to pathogen detection leverage the power of tools available in biological systems, such as highly active polymerases compatible with lyophilization, without the complexity inherent to live-cell systems, of which nucleic acid sequence based amplification (NASBA) is well known. Despite the reduced complexity associated with cell-free systems, side reactions are a common characteristic of these systems. As a result, these systems often exhibit false positives from reactions lacking an amplicon. Here we show that the inclusion of a DNA duplex lacking a promoter and unassociated with the amplicon fully suppresses false positives, enabling a suite of fluorescent aptamers to be used as NASBA tags (Apta-NASBA). Apta-NASBA has a 1 pM detection limit and can provide multiplexed, multicolor fluorescent readout. Furthermore, Apta-NASBA can be performed using a variety of equipment, for example, a fluorescence microplate reader, a qPCR instrument, or an ultra-low-cost Raspberry Pi-based 3D-printed detection platform using a cell phone camera module, compatible with field detection.
Keyphrases
- label free
- nucleic acid
- cell free
- loop mediated isothermal amplification
- real time pcr
- quantum dots
- low cost
- living cells
- stem cells
- gold nanoparticles
- sensitive detection
- signaling pathway
- gene expression
- high throughput
- air pollution
- mass spectrometry
- transcription factor
- circulating tumor
- deep learning
- convolutional neural network
- bone marrow
- fluorescent probe