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______________________________________________________________________ Introduction<br />
1.4 Hybridization detection<br />
Compared to the traditional methods for the detection of DNA sequences, such as electrophoresis<br />
or membrane blots, DNA sensors are faster, simpler and less expensive 53 , and<br />
therefore, present a very active research field. Presently, a wide range of DNA sensor<br />
technologies are in development or being commercialized.<br />
DNA sensors are based on the specific detection of a DNA sequence using a so-called probe<br />
DNA immobilized on the surface 49 (Figure 1.12). Therefore, two main parts of a DNA sensor<br />
are 48 :<br />
- biorecognition interface (immobilized specific DNA sequence) that allows the detection<br />
of a target element (complementary DNA sequence)<br />
- transducer that transforms a detected signal into a readable output<br />
Figure 1.12. Principle of a DNA sensor.<br />
The selective binding, followed by conformational and structural changes in the recognition<br />
layer, can be detected by various techniques. Depending on the transduction approach, DNA<br />
biosensors can be optical, piezoelectric and electrochemical.<br />
Optical DNA sensors based on fluorescence are very sensitive and DNA chips with this<br />
detection scheme have already been commercialized 51 . One of the optical readout strategies is<br />
the detection of an intercalating dye (e.g., ethidium bromide) upon hybridization. Furthermore,<br />
the use of molecular beacons was explored extensively (Figure 1.13). The ends of a molecular<br />
1.4 Hybridization detection 21