2. Metal-Labeled DNA on Surfaces
- Alaa S. Abd-El-Aziz2,
- Charles E. Carraher Jr.3,
- Charles U. Pittman Jr.4,
- John E. Sheats5,
- Martel Zeldin6
Published Online: 28 JUL 2004
Copyright © 2004 John Wiley & Sons, Inc.
Macromolecules Containing Metal and Metal-Like Elements: Biomedical Applications, Volume 3
How to Cite
Kraatz, H.-B., Long, Y. and Sutherland, T. C. (2004) Metal-Labeled DNA on Surfaces, in Macromolecules Containing Metal and Metal-Like Elements: Biomedical Applications, Volume 3 (eds A. S. Abd-El-Aziz, C. E. Carraher, C. U. Pittman, J. E. Sheats and M. Zeldin), John Wiley & Sons, Inc., Hoboken, NJ, USA. doi: 10.1002/0471683779.ch2
Department of Chemistry, The University of Winnipeg, Winnipeg, Manitoba, Canada
Department of Chemistry and Biochemistry, Florida Atlantic University, Boca Raton, Florida and Florida Center for Environmental Studies, Palm Beach Gardens, Florida, USA
Department of Chemistry, Mississippi State University, Mississippi State, Mississippi, USA
Department of Chemistry, Rider University, Lawrenceville, New Jersey, USA
Department of Chemistry, Hobart and William Smith Colleges, Geneva, New York, USA
- Published Online: 28 JUL 2004
- Published Print: 18 JUN 2004
Print ISBN: 9780471667377
Online ISBN: 9780471683773
- metal-labeled DNA
The self-assembly properties of DNA have been exploited to generate 2D and 3D structures on surfaces and in solution. DNA now can be modified by metal centers at individual bases or at either termini. The ability to label DNA sites specifically with metal centers allows us to influence the electronic properties of the assembly. Potential applications of these modified DNA constructs in the design of nanoelectronic or bioelectronic circuitry may be within reach. Especially, the most recent developments in the area of direct basepair metallation, such as Cu-DNA and M-DNA, allow superb control over the electronics of the DNA construct and reduce the synthetic efforts.
As shown in this review, a large driving force for research in the area of metal-DNA conjugates stems from sensor applications, for example in the detection of genetic defects, genomic fingerprinting for identification purposes, or applications in personalized medicine. Electrochemical detection methods offer a superior sensitivity to currently available optical gene chip technology. Gene chip technology has to rely on attaching a fluorescence tag to one of the DNA strands after PCR amplification. Recent advances in the area of electrochemical DNA detection described in this review should allow the development of biosensors that do not require labeling of the target DNA.
One of the holy grails of E-biosensors is the detection of single nucleotide mismatches time- and cost-effectively without the need for a lengthy PCR amplification, or in heterozygote mixtures or under non-ideal hybridization conditions. These goals are yet unrealized. Especially difficult will be the detection of DNA under “real-to-life” conditions, such as high salt concentrations or in the presence of large quantities of impurities. However, the possibility of single molecule detection using ultra-fast electrochemical techniques on ultramicroelectrodes may offer solutions to this problem.