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Issue 17, 2015
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Quantifying aptamer–protein binding via thermofluorimetric analysis

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Abstract

Effective aptamer-based protein assays require coupling to a quantitative reporter of aptamer–protein binding. Typically, this involves a direct optical or electrochemical readout of DNA hybridization or an amplification step coupled to the readout. However, method development is often hampered by the multiplicity of aptamer-target binding mechanisms, which can interfere with the hybridization step. As a simpler and more generalizable readout of aptamer–protein binding, we report that thermofluorimetric analysis (TFA) can be used to quantitatively assay protein levels. Sub-nanomolar detection (0.74 nM) of platelet-derived growth factor (PDGF) with its corresponding aptamer is shown as a test case. In the presence of various DNA intercalating dyes, protein-bound aptamers exhibit a change in fluorescence intensity compared to the intercalated, unbound aptamer. This allows thermal resolution of bound and unbound aptamers using fluorescence melting analysis (−dF/dT curves). Remarkably, the homogeneous optical method allows subtraction of autofluorescence in human serum, giving PDGF detection limits of 1.8 and 10.7 nM in serum diluted 1 : 7 and 1 : 3, respectively. We have thus demonstrated that bound and unbound aptamers can be thermally resolved in a homogeneous format using a simple qPCR instrument—even in human serum. The simplicity of this approach provides an important step toward a robust, generalizable readout of aptamer–protein binding.

Graphical abstract: Quantifying aptamer–protein binding via thermofluorimetric analysis

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Publication details

The article was received on 30 Mar 2015, accepted on 22 May 2015 and first published on 31 Jul 2015


Article type: Paper
DOI: 10.1039/C5AY00837A
Citation: Anal. Methods, 2015,7, 7358-7362
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    Quantifying aptamer–protein binding via thermofluorimetric analysis

    J. Hu, J. Kim and C. J. Easley, Anal. Methods, 2015, 7, 7358
    DOI: 10.1039/C5AY00837A

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