Erdem, ArzumCongur, GulsahEksin, Ece2019-10-272019-10-2720130925-40050925-4005https://doi.org/10.1016/j.snb.2013.07.114https://hdl.handle.net/11454/49022In the present work, a sensitive and selective enzyme-linked electrochemical sensor technology using magnetic beads assay was demonstrated for voltammetric detection of microRNAs (miRNAs) as the first time herein by using the multi-channel screen-printed array of electrodes (MUX-SPE16s). The streptavidin coated magnetic beads were used as a solid phase to immobilize biotinylated DNA capture probe, and then the complementary target RNA sequence (miRNA-15a) was recognized with the capture DNA probe. After attachment of the streptavidin-alkaline phosphatase enzyme (SALP) to biotinylated hybrid, the electroactive product a-naphthol was measured +0.188 V by linear sweep voltammetry (LSV) technique in combination with a single-use pencil graphite electrode (PGE) compared to MUX-SPE16. The oxidation signal of a-naphthol indicates the hybridization occurred between DNA probe and its RNA target in the sample. The selectivity of our assay was tested in the presence of non-complementary miRNA sequence, a very good discrimination was achieved compared to the results obtained with the full match hybridization of probe with miRNA-15a target. The detection limit of miRNA-15a target sequence was also calculated as 0.992 mu g/mL (98.60 pmole in 1 mL sample) at PGE, and 0.114 mu g/mL (34.20 fmole in 3 mu L sample) with MUX-SPE16 system. 2013 Elsevier B.V. All rights reserved.en10.1016/j.snb.2013.07.114info:eu-repo/semantics/closedAccessMulti channel screen printed array of electrodesStreptavidin-alkaline phosphatasePencil graphite electrodemiRNAMagnetic beadsMUX-SPEArticle18810891095WOS:000326345600145N/AQ1