Electrochemical primer extension based on polyoxometalate electroactive labels for multiplexed detection of single nucleotide polymorphisms

Publication date: 15 October 2018
Source:Biosensors and Bioelectronics, Volume 117
Author(s): Nassif Chahin, Laura A. Uribe, Ahmed M. Debela, Serge Thorimbert, Bernold Hasenknopf, Mayreli Ortiz, Ioannis Katakis, Ciara K. O'Sullivan
Polyoxymetalates (POMs) ([SiW11O39{Sn(CH2)2CO)}]^4- and [P2W17O61{Sn(CH2)2CO)}]^6-) were used to modify dideoxynucleotides (ddNTPs) through amide bond formation, and applied to the multiplexed detection of single nucleotide polymorphisms (SNPs) in an electrochemical primer extension reaction. Each gold electrode of an array was functionalised with a short single stranded thiolated DNA probe, specifically designed to extend with the POM-ddNTP at the SNP site to be interrogated. The system was applied to the simultaneous detection of 4 SNPs within a single stranded 103-mer model target generated using asymmetric PCR, highlighting the potential of POM-ddNTPs for targeted, multiplexed SNP detection. The four DNA bases were successfully labelled with both ([SiW11O39{Sn(CH2)2CO)}]^4- and [P2W17O61{Sn(CH2)2CO)}]^6-), and [SiW11O39{Sn(CH2)2CO)}]^4- demonstrated to be the more suitable due to its single oxidation peak, which provides an unequivocal signal. The POM-ddNTP enzymatically incorporated to the DNA anchored to the surface was visualised by AFM using gold coated mica. The developed assay has been demonstrated to be highly reproducible, simple to carry out and with very low non-specific background signals. Future work will focus on applying the developed platform to the detection of SNPs associated with rifampicin resistance in real samples from patients suffering from tuberculosis.

Graphical abstract

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