2009
DOI: 10.1007/s00216-009-3374-8
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SERS as tool for the analysis of DNA-chips in a microfluidic platform

Abstract: A sequence-specific detection method of DNA is presented combining a solid chip surface for immobilisation of capture DNAs with a microfluidic platform and a readout of the chip based on SERS. The solid chip surface is used for immobilisation of different capture DNAs, where target strands can be hybridised and unbound surfactants can be washed away. For the detection via SERS, short-labelled oligonucleotides are hybridised to the target strands. This technique is combined with a microfluidic platform that ena… Show more

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Cited by 58 publications
(44 citation statements)
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“…3 is generally in agreement with those reported earlier [21] showing characteristic Raman lines at 739 cm À1 and 1339 cm À1 corresponding to the purine ring breathing mode and CN stretching mode, respectively. The ultra-sensitive detection of adenine suggests that monitoring of DNA sequencing on the single-molecule level is possible on this engineered substrate after further optimization to attain higher detection limitation or detecting the mismatch of DNA sequences after the integration to a chip-based platform [22,23]. For further confirmation, adenosine is chosen as another target molecule because of the important role played by adenosine triphosphate (ATP) molecules in biological energyetransfer reactions.…”
Section: Resultsmentioning
confidence: 99%
“…3 is generally in agreement with those reported earlier [21] showing characteristic Raman lines at 739 cm À1 and 1339 cm À1 corresponding to the purine ring breathing mode and CN stretching mode, respectively. The ultra-sensitive detection of adenine suggests that monitoring of DNA sequencing on the single-molecule level is possible on this engineered substrate after further optimization to attain higher detection limitation or detecting the mismatch of DNA sequences after the integration to a chip-based platform [22,23]. For further confirmation, adenosine is chosen as another target molecule because of the important role played by adenosine triphosphate (ATP) molecules in biological energyetransfer reactions.…”
Section: Resultsmentioning
confidence: 99%
“…[13] Compared to chip-based methods [14][15][16][17][18][19][20][21][22] the use of magnetic particles benefits from improved hybridization kinetics. By employing biotin-labeled primers for the amplification of target DNA with polymerase chain reaction (PCR), the PCR products can bind directly onto the magnetic beads.…”
Section: Magnetic Particlesmentioning
confidence: 99%
“…To solve this situation, single-and doublestranded thiolated DNA or RNA oligomers have been used, which can direct the adsorption of the macromolecule to be perpendicular to the surface (Barhoumi et al 2008). Further, other recent approaches include the combination of SERS with microfluidic systems for sequence-specific detection of DNA (Strelau et al 2010).…”
Section: Direct Sers Sensingmentioning
confidence: 99%