A Better Test To Detect DNA For Diagnosing Disease, Investigating Crimes

Main Category: Biology / Biochemistry
Also Included In: Medical Devices / Diagnostics
Article Date: 27 Aug 2009 - 1:00 PDT

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Researchers in Singapore are reporting development of a new electronic sensor that shows promise as a faster, less expensive, and more practical alternative than tests now used to detect DNA. Such tests are done for criminal investigation, disease diagnosis, and other purposes. The new lab-on-a-chip test could lead to wider, more convenient use of DNA testing, the researchers say. Their study is scheduled for the Sept. 2 issue of the Journal of the American Chemical Society, a weekly publication.

In the new study, Zhiqiang Gao and colleagues note that current methods for detecting DNA involve the used of the polymerase chain reaction (PCR). This technique "amplifies" or makes multiple copies of trace amounts of DNA, much as a photocopier produces multiple copies of documents, in order to detect the genetic material more easily. The amplification step is one reason why tests involving PCR can be too expensive, cumbersome, and imprecise for wider use.

The researchers describe development of a so-called "nanogap sensor" that appears to overcome those obstacles. The process uses a pair of micro-sized metal electrodes separated by a nanogap, 1/50,000 the width of a human hair, in combination with special chemical probes to capture tiny segments of DNA. The newly formed "circuit" then translates the presence of DNA into an electrical signal so that it can be measured by a computer. In laboratory tests, the sensor showed "excellent" sensitivity at detecting trace amounts of human DNA and may eliminate the need for DNA amplification altogether, the researchers say.

Source
Journal of the American Chemical Society

Article adapted by Medical News Today from original press release.
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Journal of the American Chemical Society. "A Better Test To Detect DNA For Diagnosing Disease, Investigating Crimes." Medical News Today. MediLexicon, Intl., 27 Aug. 2009. Web.
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