Fast detection of mycoplasma pneumoniae by interaction of tetramolecular G-quadruplex with graphene oxide
[Display omitted] •The interaction of tetrapod G-quadruplex (TP-G4) with graphene oxide (GO) is found to induce its adsorption on GO.•The adsorption of TP-G4 on GO quenches the fluorescence of the dye labelled to TP-G4.•A biosensing platform is designed based on the interaction of TP-G4 with GO and...
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Veröffentlicht in: | Sensors and actuators. B, Chemical Chemical, 2019-07, Vol.290, p.41-46 |
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Format: | Artikel |
Sprache: | eng |
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•The interaction of tetrapod G-quadruplex (TP-G4) with graphene oxide (GO) is found to induce its adsorption on GO.•The adsorption of TP-G4 on GO quenches the fluorescence of the dye labelled to TP-G4.•A biosensing platform is designed based on the interaction of TP-G4 with GO and the recognition of TP-G4 to target.•A fast fluorescent detection method is developed for mycoplasma pneumoniae down to 3.96 nM.•The TP-G4 can be conveniently used as a versatile biosensing probe for different DNA analytes.
Fast and sensitive detection of mycoplasma pneumoniae (MP) is quite momentous in early diagnosis of respiratory infections. Herein, we present a new biosensing platform for MP based on the interaction of a designed parallel-stranded tetrapod G-quadruplex (TP-G4) with graphene oxide. The G-quadruplex is formed with four fluorescent dye labeled ssDNA molecules, which is demonstrated with gel electrophoresis, CD spectra and fluorescence spectra. The interaction induces the adsorption of TP-G4 on graphene oxide, which leads to the fluorescence quenching of the dye. Upon the recognition of the adsorbed ends to target MP, the TP-G4 can be released from graphene oxide surface, producing a “signal-on” fluorescence biosensor for MP. The designed biosensing strategy shows a detection limit of 3.96 nM and an analytical time of 10 min. The facile and fast operation process and acceptable sensitivity meet the demands of early point-of-care testing of mycoplasma pneumoniae, showing its promising application in clinic diagnosis. |
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ISSN: | 0925-4005 1873-3077 |
DOI: | 10.1016/j.snb.2019.03.103 |