In force spectroscopy single-molecule experiments, an individual molecule, usually a polymer, is mechanically stretched by means of an externally controlled driving potential. Typically, the stiffness of this potential is much smaller than the stiffness of the potential of mean force along the molecular extension coordinate. Here we discuss how such a disparity alters the free energy and the reversibility of the driven system, with respect to the pristine molecular system under examination. In particular, by simulating unfolding/refolding experiments of a small protein, we examine the traits of the potential of mean force that are responsible for the dramatic amount of work dissipated in experiments using a soft device. Finally, we show that in bidirectional experiments the free energy of the free molecular system can be easily recovered by appropriate reweighting methods.
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