A near-field scanner
for moving molecules has been built and demonstrated
by a multinational research team (Robert Austin, Princeton, 609-258-4353,
rha@suiling.princeton.edu),
offering a potentially fast way to make high-resolution images of molecules
such as DNA. Traditional scanning-probe
microscopes offer molecular-level images, but at the cost of slow scanning
speeds for large molecules.
In the new device,
molecules travel in a microscopic fluid channel (5 microns wide by 1
micron deep) and pass directly under a trio of 100-nm-wide slits that
are just a few hundred nanometers above the molecules. The fluid channel
contains an array of posts to stretch out the DNA molecules. A laser
causes the molecules to fluoresce, providing light that yields an image.
The slits' narrow width, along with their proximity to the molecules,
enables high-resolution images, 200-nm resolution in this initial experiment.
To ensure high-quality
images, the microscope accepts data only from those molecules that pass
through the three slits at roughly equal time intervals.
For a DNA molecule
with 200,000 base pairs (corresponding to about 74 microns in stretched
form), the researchers obtained imaging data in just 100 milliseconds,
considerably faster than AFM or traditional near-field optical microscopes.
Resolution improvements are possible by narrowing the slits or making
them thinner; future versions of the device will employ shallower fluid
channels for confining DNA molecules to a greater degree.
Ultimately, the
researchers envision massively parallel data acquisition by creating
multiple slits that simultaneously scan many molecules. This microscope
design could potentially obtain high-resolution maps of the binding
sites of repressor/promoter proteins critical for the expression of
genes, part of an emerging field called epigenetics. (Tegenfeldt
et al., Physical Review
Letters, 12 February 2001.)