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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

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