AI Article Synopsis

  • A new nanoparticle-based chemiluminescent method has been created for ultrasensitive DNA hybridization detection, using silver nanoparticles and oligonucleotide probes.
  • The method achieves detection levels as low as 5 fM, significantly surpassing traditional gold nanoparticle colorimetric techniques and rivaling advanced methods like surface-enhanced Raman spectroscopy.
  • It can also distinguish between perfectly complementary DNA strands and single-base mismatched strands by adjusting temperature, making it promising for assessing single-nucleotide polymorphisms.

Article Abstract

A new nanoparticle-based chemiluminescent (CL) method has been developed for the ultrasensitive detection of DNA hybridization. The assay relies on a sandwich-type DNA hybridization in which the DNA targets are first hybridized to the captured oligonucleotide probes immobilized on polystyrene microwells and then the silver nanoparticles modified with alkylthiol-capped oligonucleotides are used as probes to monitor the presence of the specific target DNA. After being anchored on the hybrids, silver nanoparticles are dissolved to Ag+ in HNO3 solution and sensitively determined by a coupling CL reaction system (Ag+-Mn2+-K2S2O8-H3PO4-luminol). The combination of the remarkable sensitivity of the CL method with the large number of Ag+ released from each hybrid allows the detection of specific sequence DNA targets at levels as low as 5 fM. The sensitivity increases 6 orders of magnitude greater than that of the gold nanoparticle-based colorimetric method and is comparable to that of surface-enhanced Raman spectroscopy, which is one of the most sensitive detection approaches available to the nanoparticle-based detection for DNA hybridization. Moreover, the perfectly complementary DNA targets and the single-base mismatched DNA strands can be evidently differentiated through controlling the temperature, which indicates that the proposed CL assay offers great promise for single-nucleotide polymorphism analysis.

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Source
http://dx.doi.org/10.1021/ac0522409DOI Listing

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