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Harold G Craighead

Publications and source records attributed to Harold G Craighead.

3 recordsLinked to original sources

DNA fragment sizing by single molecule detection in submicrometer-sized closed fluidic channels.

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.

DNA↗

Liquid-crystal micropolarizer array for polarization-difference imaging.

Fabrication and applications are discussed for a visible-wavelength micropolarizer array consisting of a linear polarizer and a micropatterned liquid-crystal (LC) cell. LC alignment direction is controlled by means of depositing an optically transparent gold film at an oblique angle and coating the surface with an alkanethiol self-assembled monolayer. Microdomains of two perpendicular LC alignment directions are created by photolithography and etching of the gold layer, rotating the substrate 90 deg, and depositing a second oblique gold layer in the etched areas. The resulting array is used for polarization-difference imaging (PDI), a technique that enhances image contrast in the presence of scattering. Images obtained with the array require more processing than do conventional PDI images, but this method eliminates the need for an electronically activated LC filter and is especially suited to systems whose filters are closely integrated with optical sensor arrays.

Journal Article↗

Characterization and optimization of an entropic trap for DNA separation.

Recently, a microfabricated entropic trap array was demonstrated to be useful in separating large (5-200 kbp) DNA molecules efficiently (within approximately 30 min), by dc electrophoresis, on a microchip platform without a sieving matrix. This paper reports further development of the technique, with emphasis on optimizing separation selectivity and resolution. The interaction of DNA molecules with regularly spaced entropic barriers was modeled in order to predict the effect of changing various structural parameters. The selectivity (differential mobility) was shown to be dependent on the depth of deep and shallow channel regions, applied electric field, and number of entropic barriers. Experimental data were compared with the prediction of the model. It was expected from the model that, in the low-field (severe trapping) limit, separation resolution should depend only on the number of entropic traps. However, in reality, resolution did depend on the applied field because the relaxation of DNA is not achieved at high fields. The requirement and feasibility of megabase pair DNA separation with the entropic trap array device was discussed.

DNA↗