Magnetic bead-based hybridization assay for electrochemical detection of microRNA
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
24528657
DOI
10.1016/j.aca.2014.01.023
PII: S0003-2670(14)00069-5
Knihovny.cz E-zdroje
- Klíčová slova
- Electrochemistry, Mercury electrodes, MicroRNA, Mismatch discrimination,
- MeSH
- 2,2'-dipyridyl analogy a deriváty chemie MeSH
- biosenzitivní techniky metody MeSH
- biotinylace MeSH
- elektrochemické techniky metody MeSH
- hybridizace nukleových kyselin metody MeSH
- lidé MeSH
- limita detekce MeSH
- magnetické jevy MeSH
- mikro RNA analýza MeSH
- organokovové sloučeniny chemie MeSH
- rtuť chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2,2'-dipyridyl MeSH
- mikro RNA MeSH
- organokovové sloučeniny MeSH
- osmium tetroxide-2,2'-bipyridine MeSH Prohlížeč
- rtuť MeSH
Aberrant expression of microRNAs (miRNAs), short non-coding RNA molecules regulating gene expression, is often found in tumor cells, making the miRNAs suitable candidates as cancer biomarkers. Electrochemistry is an interesting alternative to current standard methods of miRNA detection by offering cheaper instrumentation and faster assays times. In this paper, we labeled miRNA in a quick, simple, two-step procedure with electroactive complex of osmium(VI) and 2,2'-bipyridine, Os(VI)bipy, which specifically binds to the ribose at the 3'-end of the miRNA, and hybridized such labeled miRNA with biotinylated capture probe attached to the streptavidin magnetic beads. Labeled miRNA was then detected at hanging mercury drop electrode at femtomole level due to an electrocatalytic nature of the peak from the Os(VI)bipy label. We obtained good selectivity of the assay using elevated hybridization temperatures for better discrimination of perfect duplex from single and double mismatches. After optimization of the protocol, we demonstrated feasibility of our assay by detecting target miRNA in real total RNA samples isolated from human cancer cells.
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