Ligand‐Induced Folding in a Dopamine‐Binding DNA Aptamer
Yunus A. Kaiyum, Emily Hoi Pui Chao, Lakshmi Dhar, Aron A. Shoara, Minh‐Dat Nguyen, Cameron D. Mackereth, Philippe Dauphin‐Ducharme, Philip E. Johnson
Abstract
Abstract Aptamers are often employed as molecular recognition elements in the development of different types of biosensors. Many of these biosensors take advantage of the aptamer having a ligand‐induced structure‐formation binding mechanism. However, this binding mechanism is poorly understood. Here we use isothermal titration calorimetry, circular dichroism spectroscopy and NMR spectroscopy to study the binding and ligand‐induced structural change exhibited by a dopamine‐binding DNA aptamer. We analysed a series of aptamers where we shorten the terminal stem that contains the 5' and 3' termini of the aptamer sequence. All aptamers bind dopamine in an enthalpically driven process coupled with an unfavorable entropy. A general trend of the aptamer having a weaker binding affinity is observed as the terminal stem is shortened. For all aptamers studied, numerous signals appear in the imino region of the 1 H NMR spectrum indicating that new structure forms with ligand binding. However, it is only when this region of structure formation in the aptamer is brought close to the sensor surface that we obtain a functional electrochemical aptamer‐based biosensor.