Litcius/Paper detail

Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout

Lauren M. Aufdembrink, Pavana Khan, Nathaniel J. Gaut, Katarzyna P. Adamala, Aaron E. Engelhart

2020RNA25 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

NASBAAmpliconAptamerBiologyLoop-mediated isothermal amplificationComputational biologyMolecular beaconFalse positive paradoxFluorescenceMolecular biologyDNAPolymerase chain reactionComputer scienceOligonucleotideGeneticsNucleic acid sequencePhysicsMachine learningGeneQuantum mechanicsAdvanced biosensing and bioanalysis techniquesBiosensors and Analytical DetectionAdvanced Biosensing Techniques and Applications