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Highly specific, multiplexed isothermal pathogen detection with fluorescent aptamer readout.

Authors :
Aufdembrink LM
Khan P
Gaut NJ
Adamala KP
Engelhart AE
Source :
RNA (New York, N.Y.) [RNA] 2020 Sep; Vol. 26 (9), pp. 1283-1290. Date of Electronic Publication: 2020 Jun 01.
Publication Year :
2020

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.<br /> (© 2020 Aufdembrink et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society.)

Details

Language :
English
ISSN :
1469-9001
Volume :
26
Issue :
9
Database :
MEDLINE
Journal :
RNA (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
32482894
Full Text :
https://doi.org/10.1261/rna.075192.120