Following Single Molecules by Force Spectroscopy
Dynamic force spectroscopy of single molecules, in which an adhesion bond is driven away from equilibrium by a spring pulled with velocity V, is described by a model that predicts the distribution of rupture forces (mean and variance), all amenable to experimental tests. The distribution has a prono...
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Veröffentlicht in: | Israel journal of chemistry 2004-12, Vol.44 (4), p.363-372 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Dynamic force spectroscopy of single molecules, in which an adhesion bond is driven away from equilibrium by a spring pulled with velocity V, is described by a model that predicts the distribution of rupture forces (mean and variance), all amenable to experimental tests. The distribution has a pronounced asymmetry, which has recently been observed experimentally. The mean rupture force follows a (lnV)2/3 dependence on the pulling velocity and differs from earlier predictions. Interestingly, at low pulling velocities a rebinding process is observed whose signature is an intermittent behavior of the spring force that delays the rupture. Based on the rupture mechanism, we propose a new “pick‐up‐and‐put‐down” method to manipulate individual molecules with scanning probes. We demonstrate that the number of molecules picked up by the tip and deposited at a different location can be controlled by adjusting the pulling velocity of the tip and the distance of closest approach of the tip to the surface. |
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ISSN: | 0021-2148 1869-5868 |
DOI: | 10.1560/TBV9-439H-6U1D-1BDX |