Generation of nanomechanical cantilever motion from biomolecular interactio
ns can have wide applications, ranging from high-throughput biomolecular de
tection to bioactuation, Although it has been suggested that such motion is
caused by changes in surface stress of a cantilever beam, the origin of th
e surface-stress change has so far not been elucidated. By using DNA hybrid
ization experiments, we show that the origin of motion lies in the interpla
y between changes in configurational entropy and intermolecular energetics
induced by specific biomolecular interactions. By controlling entropy chang
e during DNA hybridization, the direction of cantilever motion can be manip
ulated. These thermodynamic principles were also used to explain the origin
of motion generated from protein-ligand binding.