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Quicker, Cheaper SARS Virus Detector -- One Easily Customizable For Other Targets

Date:
June 1, 2009
Source:
University of Southern California
Summary:
Researchers say they've made a big improvement in a new breed of electronic detectors for viruses and other biological materials -- one that may be a valuable addition to the battle against epidemics.

Antibody mimic protein is tailored to attach to nanowire base at one end, leaving biologically active area open for detection.
Credit: University of Southern California

Members of a USC-led research team say they've made a big improvement in a new breed of electronic detectors for viruses and other biological materials — one that may be a valuable addition to the battle against epidemics.

It consists of a piece of synthetic antibody attached to a nanowire that's attached to an electrical base, immersed in liquid.

If the protein the antibody binds to is present in the liquid, it will bind to these antibodies, immediately creating a sharply measurable jump in current through the nanowire.

The basic principle of nanotube and nanowire biosensors for protein detection was first demonstrated in 2001, but the new design by a team headed by Zhongwu Chou and Mark Thompson of the University of Southern California uses two new elements.

First, it takes advantage of bioengineered synthetic antibodies, much, much smaller versions of the natural substances that are designed to bind with a specific protein and only that protein.

Second, it uses indium oxide (In2O3) nanowires instead of silicon and other materials previously tried. Metal oxides, according to a new study published in ACS Nano, do not, unlike silicon, develop "an insulating native oxide layer that can reduce sensitivity."

The result, according to the paper, is a device that can detect its target molecules with a sensitivity as great as the best alternative modes, do so more rapidly and without use of chemical reagents.

It is also potentially considerably cheaper than alternatives.

"We believe," the authors write, "that nanowire bisensor devices functionalized with engineered proteins … can have important applications ranging from disease diagnosis to homeland security."

Additionally, the system can be useful in basis research, in helping to establish certain important parameters for two-part biological systems like the antibody/target protein pair.

The protein the prototype system detects is the SARS (severe acute respiratory syndrome) virus n-protein, which infected more than 8,000 people in 2002-2003, killing nearly 10 percent of them.

Commercial systems using enzyme-linked immunosorbent assay (ELISA) now exist to test for SARS, but the new system has advantages in time, cost and portability.

The first step was the creation, by Richard Roberts and Mark Thompson, chemists, and their team of the synthetic antibody, including both the active area, design to interact with the protein and, at the other end, a chemical "hook" that would bind it to nanowire at this point and only this point. "This … strategy allows every bound [detector molecule] to retain full activity, a clear advantage over antibodies, which [in earlier biosensor designs] are often bound to nanowire surface via amine containing residues randomly distributed over the antibody surface."

The Zhou lab, which has specialized in nanowire and nanotube technology for years, performed the complex set of procedures to synthesize the wires, attaching

In tests, the group performed if anything better than predictions, showing a standard and low level of activity when no SARS protein was present, leaping quickly to a higher level when the protein was introduced, in response patterns that varied consistently according to concentration of the SARS protein. Devices complete except for the detector molecule showed no response at all.

The response was complete in less than ten minutes, compared to hours needed for results from ELISA tests - which are basically present/not present tests with relatively little quantitative elements.

Next steps are to enable detection in more complex environment, such as Serum and whole blood, by integrating the nanobiosensor with micro systems such as microfluidics chips and micro filters.

The USC team believes their new system has potential to be cheaper and more portable than either.

In addition to Zhou (from the Viterbi School's Ming Hsieh Department of Electrical Engineering) and Thompson (of the USC College Department of Chemistry), the team included Fumiaki Ishikawa, Hsaio-Kang Chang, Po-Ching Chen from Electrical Engineering; Marco Curreli, Rui Zhang, Richard W. Roberts and C. Anders Olson from Chemistry, Richard J. Cote of the Keck School of Medicine at USC Department of Pathology, and Hsiang-I Liao and Ren Sun of the UCLA Department of Medical Pharmacology.

The Whittier Foundation and the National Institutes of Health funded the research.


Story Source:

The above story is based on materials provided by University of Southern California. Note: Materials may be edited for content and length.


Journal Reference:

  1. Fumiaki N. Ishikawa, Hsiao-Kang Chang, Marco Curreli, Hsiang-I Liao, C. Anders Olson, Po-Chiang Chen, Rui Zhang, Richard W. Roberts, Ren Sun, Richard J. Cote, Mark E. Thompson and Chongwu Zhou. Label-Free, Electrical Detection of the SARS Virus N-Protein with Nanowire Biosensors Utilizing Antibody Mimics as Capture Probes. ACS Nano, 2009; 3 (5): 1219 DOI: 10.1021/nn900086c

Cite This Page:

University of Southern California. "Quicker, Cheaper SARS Virus Detector -- One Easily Customizable For Other Targets." ScienceDaily. ScienceDaily, 1 June 2009. <www.sciencedaily.com/releases/2009/05/090529093152.htm>.
University of Southern California. (2009, June 1). Quicker, Cheaper SARS Virus Detector -- One Easily Customizable For Other Targets. ScienceDaily. Retrieved July 28, 2014 from www.sciencedaily.com/releases/2009/05/090529093152.htm
University of Southern California. "Quicker, Cheaper SARS Virus Detector -- One Easily Customizable For Other Targets." ScienceDaily. www.sciencedaily.com/releases/2009/05/090529093152.htm (accessed July 28, 2014).

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