Abstract
The exponential amplification reaction (EXPAR) is an emerging isothermal nucleic acid amplification method with high potential for molecular diagnostics due to its isothermal nature and high amplification efficiency. However, the use of EXPAR is limited by the high levels of non-specific amplification. Hence, methods that can improve the specificity of EXPAR are desired to facilitate its widespread adoption in practice. Herein, we proposed a strategy to improve EXPAR performance by using molecular enhancers. Eight small molecules were investigated, including ethylene glycol, propylene glycol, betaine, dimethyl sulfoxide (DMSO), trehalose, tetramethylammonium chloride (TMAC), bovine serum albumin (BSA) and single-stranded binding (SSB) proteins. A combination of kinetic and end-point analysis was adopted to investigate how these molecules affected EXPAR performance. Trehalose, TMAC, BSA and SSB proteins were found to have positive effects on EXPAR with trehalose being able to increase the efficiency of EXPAR. In contrast, TMAC, BSA and SSB proteins were shown to increase the specificity of EXPAR. We applied our findings to demonstrate the combination of trehalose and TMAC could simultaneously improve both the efficiency and specificity of an EXPAR-based miRNA detection method. The information provided in this study may serve as a reference to benefit the wider isothermal amplification community.
Highlights
The exponential amplification reaction (EXPAR) is an emerging isothermal nucleic acid amplification method with high potential for molecular diagnostics due to its isothermal nature and high amplification efficiency
We investigated the effects of several small molecules including ethylene glycol, propylene glycol, betaine, dimethyl sulfoxide (DMSO), trehalose, tetramethylammonium chloride (TMAC), bovine serum albumin (BSA) and single-stranded binding (SSB) proteins on EXPAR
The effects of several small molecules on EXPAR were studied in this work to investigate their potential to enhance EXPAR by increasing reaction efficiency and specificity
Summary
Very similar results were obtained for propylene glycol, betaine and DMSO in which higher concentration of these small molecules increased specificity (see Supplementary Figures S4, S5 and S6) From the real time experiments, the combination of trehalose and TMAC did not seem to affect the rate of EXPAR over the individual additives as all target-dependent amplification were detected within a similar time frame (Fig. 4A). Under current EXPAR conditions, 1.8 M ethylene glycol, 0.8 M propylene glycol, 1 M betaine, 5% DMSO, 0.4 M trehalose and 40 mM TMAC lowered the Tm between target and template by at least 2 °C Each of those small molecules decreased Tm to different degrees, consistent with the literature[15,22,32,33,34,35].
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