AI Article Synopsis

  • The text describes the creation of tiny fluidic channels (smaller than 1 micrometer) for detecting individual DNA molecules, using a method that ensures low background noise and precise control over channel dimensions.
  • These channels enhance single molecule detection by preventing multiple molecules from passing through simultaneously, and it was found that DNA can move through these channels at speeds of up to 5 mm/s under an electric field.
  • A single experiment can analyze different DNA fragments and their concentrations using only about 10,000 molecules, highlighting the efficiency and potential broader applications of these microstructures in DNA analysis.

Article Abstract

The fabrication of fluidic channels with dimensions smaller than 1 microm is described and characterized in respect to their use for detection of individual DNA molecules. The sacrificial layer technique is used to fabricate these devices as it provides CMOS-compatible materials exhibiting low fluorescence background. It also allows creating microfluidics circuitry of submicrometer dimensions with great control. The small dimensions facilitate single molecule detection and minimize events of simultaneous passage of more than one molecule through the measurement volume. The behavior of DNA molecules inside these channels under an applied electrical field was first studied by fluorescence correlation spectroscopy using M13 double-stranded DNA. A linear relationship between the flow speed and applied electric field across the channel was observed. Speeds as high as 5 mm/s were reached, corresponding to only a few milliseconds of analysis time per molecule. The channels were then used to characterize a mixture of nine DNA fragments. Both the distribution and relative proportions of the individual fragments, as well as the overall concentration of the DNA sample, can be deduced from a single experiment. The amount of sample required for the analysis was approximately 10,000 molecules, or 76 fg. Other potential applications of these submicrometer structures for DNA analysis are discussed.

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http://dx.doi.org/10.1021/ac011076wDOI Listing

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