Improving DNA sequencing: Sponge-like biosensor crams enormous power into tiny space

(Press-News.org) WASHINGTON, May 26—Vanderbilt University engineers have created a "spongy" silicon biosensor that shows promise not only for medical diagnostics, but also for the detection of dangerous toxins and other tiny molecules in the environment. This innovation was originally designed to detect the presence of particular DNA sequences, which can be extremely helpful in identifying whether or not a person is predisposed to heart disease or certain kinds of cancer. The new sensor is described in the Optical Society's open access journal, Optics Express.

Biological chemical sensors save lives by detecting dangerous substances in the environment or specific molecules in the blood that could signal life-threatening diseases. Current sensor technologies, however, are limited because of their large size compared to the extremely minute sizes of some of the chemicals to be detected. In most cases, when attempting to sense something very small with a large sensor, the small molecules don't perturb the sensor's properties enough for detection.

As Vanderbilt University's Xing Wei, a graduate student, and Sharon M. Weiss, an associate professor of electrical engineering and physics, report in Optics Express, it's possible to eliminate this challenge by making sensors with features that are comparative in size to the molecules being detected, greatly increasing the sensitivity of current sensing technology.

To do this, the engineers turned to a porous silicon material, which acts essentially as a small sponge that can then be "seeded" or filled with all sorts of substances that change its properties—resulting in a detector that's highly sensitive to small molecules (See Figure 1). Capturing a particular sequence of DNA involves seeding the sensor with a single strand of DNA, so that only the complementary strand can attach to it and everything else gets rinsed away.

Why use a porous silicon material? Weiss and Wei stress the significance of their new sensor's enormous surface area relative to its small size. To illustrate this point, Weiss describes two cubes, one of which is 3 cm on a side, with a flat surface that DNA can be attached to—providing 54 cm2 of available surface area to attach these molecules. The other is an identical-size cube, made into a porous silicon sponge and with the ability to access the volume of the cube with all of the internal surface area, providing a surface area that is nearly 10,000 times greater than the first cube. This is like comparing the area of a golf ball to the area of a football field—with the same footprint (See Figure 2). "It's an enormous increase in the potential of how many molecules you can capture, and this is one reason why our new sensor is so much more sensitive for detecting small molecules," says Weiss.

And by using a "grating," a type of surface texturing of the porous silicon commonly used in sensors of this type, light can be delivered in a very simple and compact way to probe the change in the sensor's properties to determine whether or not any molecules of interest have been captured.

"If you look at a CD or a DVD in the light, you'll notice lots of colors bounce off it in room light. The way these discs work is that there are a bunch of bumps, which are very similar to our gratings," says Weiss. When light interacts with a particular arrangement of bumps, the engineers can essentially tell the light what to do, enabling readout of the music or videos on the disc.

That's precisely what the Vanderbilt team has done with their sensor—put bumps on top of it to control how the light interacts with their active sensing medium (the porous silicon "waveguide"). Then they can determine what the signal means based either on the color that comes out or by the angle of light as it exits the sensor.

"When we infiltrate the molecules that we want to detect and they stay in the sensor and attach, they change the optical density of the porous silicon and, consequently, the angle or the color of light that comes back out," Weiss elaborates. "By knowing how much the angle changes, for example, we can quantify how many molecules are present. So not only can we identify our DNA sequence or toxin, but we can also know how much is present as well. For diagnostics, it's very helpful to know how much is present."

Other potential applications beyond DNA sensing may include detecting small molecules—such as toxins in the environment—which has significant national security implications.



INFORMATION:

Paper: "Guided mode biosensor based on grating coupled porous silicon waveguide," Xing Wei and Sharon M. Weiss, Optics Express, Volume 19, Issue 12, pp. 11330-11339. http://www.opticsinfobase.org/oe/abstract.cfm?uri=oe-19-12-11330

About Optics Express

Optics Express reports on new developments in all fields of optical science and technology every two weeks. The journal provides rapid publication of original, peer-reviewed papers. It is published by the Optical Society and edited by C. Martijn de Sterke of the University of Sydney. Optics Express is an open-access journal and is available at no cost to readers online at http://www.OpticsInfoBase.org/OE.

About OSA

Uniting more than 106,000 professionals from 134 countries, the Optical Society (OSA) brings together the global optics community through its programs and initiatives. Since 1916 OSA has worked to advance the common interests of the field, providing educational resources to the scientists, engineers and business leaders who work in the field by promoting the science of light and the advanced technologies made possible by optics and photonics. OSA publications, events, technical groups and programs foster optics knowledge and scientific collaboration among all those with an interest in optics and photonics. For more information, visit www.osa.org.