The development of instrument-free, PCR-less, ultrasensitive and selective DNA detection methods is highly desired in chemical and life sciences. Herein we report on the utility of a biomineralization-assisted amplification methodology for the identification of DNA. Significantly, the diagnostic strategy has allowed the target detection at a concentration as low as 50 aM, equivalent to similar to 180 copies in the entire 6 mu L sample. In addition, the DNA sequence with a single-base mismatch can be differentiated from the perfect target through a facile salt-based stringency wash. Substitution of the DNA structures with other recognition moieties should allow the translation of the strategy to the assay of different targets of interest. The visual readout format provides a sound basis for the broad applicability of the proposed strategy, especially in resource-poor settings.
机构:
Univ So Calif, Dept Chem, Los Angeles, CA 90089 USAUniv Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
Brutchey, Richard L.
Morse, Daniel E.
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Univ Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USAUniv Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
机构:
Univ So Calif, Dept Chem, Los Angeles, CA 90089 USAUniv Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
Brutchey, Richard L.
Morse, Daniel E.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USAUniv Calif Santa Barbara, Mat Res Lab, Calif NanoSyst Inst, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA