Information-to-work conversion in single-molecule experiments: From discrete to continuous feedback.

We theoretically investigate the extractable work in single molecule unfolding-folding experiments with applied feedback. Using a simple two-state model, we obtain a description of the full work distribution from discrete to continuous feedback. The effect of the feedback is captured by a detailed fluctuation theorem, accounting for the information aquired.

Experimental Test of Sinai's Model in DNA Unzipping.

The experimental measurement of correlation functions and critical exponents in disordered systems is key to testing renormalization group (RG) predictions. We mechanically unzip single DNA hairpins with optical tweezers, an experimental realization of the diffusive motion of a particle in a one-dimensional random force field, known as the Sinai model. We measure the unzipping forces F_{w} as a function of the trap position w in equilibrium and calculate the force-force correlator Δ_{m}(w), its amplitude, and correlation length, finding agreement with theoretical predictions.

Temperature-dependent elastic properties of DNA.

Knowledge of the elastic properties, e.g., the persistence length or interphosphate distance, of single-stranded (ss) and double-stranded (ds) DNA under different experimental conditions is critical to characterizing molecular reactions studied with single-molecule techniques.

Folding Free Energy Determination of an RNA Three-Way Junction Using Fluctuation Theorems.

Nonequilibrium work relations and fluctuation theorems permit us to extract equilibrium information from nonequilibrium measurements. They find application in single-molecule pulling experiments where molecular free energies can be determined from irreversible work measurements by using unidirectional (e.g.

Molten globule-like transition state of protein barnase measured with calorimetric force spectroscopy.

SignificanceUnderstanding the molecular forces driving the unfolded polypeptide chain to self-assemble into a functional native structure remains an open question. However, identifying the states visited during protein folding (e.g.