Aptamers are known to generally undergo a conformational change upon binding to their ligand. This can be exploited for their selection and for signaling the presence of the target. The structural change is then associated to a signal (fluorescence energy transfer for instance). This can be deliberately exploited for the design of aptamer-based biosensors.
The selection is carried out against free molecules in solution whereas the oligonucleotide library is immobilized in a support. Candidates released in the solution following the addition of the target molecule are collected, amplified and analyzed. In another format the selection takes advantage of so-called kissing interactions. In this case, the addition of the target promotes the interaction of candidates to a hairpin oligonucleotide that are subsequently collected, amplified and analyzed. The selected candidates are functional aptaswitch. They can be integrated into biosensors with different modalities of signal transduction.
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