An increasing number of inter- and intramoleculor interactions can nowadays be probed using single-molecule manipulation techniques. Protein unfolding and refolding is the most representative-though complex-of these interactions. Herein, we review the main modes of performing a force unfolding experiment: the velocity clamp and the new force clamp mode. We con also compare some of the physical aspects behind the two most frequently used single-molecule manipulation instrumentations: optical tweezers and atomic force microscopes.

Protein unfolding and refolding under force: Methodologies for nanomechanics

Zuccheri G;Baschieri P
2005

Abstract

An increasing number of inter- and intramoleculor interactions can nowadays be probed using single-molecule manipulation techniques. Protein unfolding and refolding is the most representative-though complex-of these interactions. Herein, we review the main modes of performing a force unfolding experiment: the velocity clamp and the new force clamp mode. We con also compare some of the physical aspects behind the two most frequently used single-molecule manipulation instrumentations: optical tweezers and atomic force microscopes.
2005
atomic force microscopes
DNA structures
optical tweezers
protein folding
single-molecule studies
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/347507
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