Literature DB >> 18352091

Analyzing single-bond experiments: influence of the shape of the energy landscape and universal law between the width, depth, and force spectrum of the bond.

Julien Husson1, Frédéric Pincet.   

Abstract

Experimentalists who measure the rupture force of a single molecular bond usually pull on that bond at a constant speed, keeping the loading rate r=df/dt constant. The challenge is to extract the energy landscape of the interaction between the two molecules involved from the experimental rupture force distribution under several loading rates. This analysis requires the use of a model for the shape of this energy landscape. Several barriers can compose the landscape, though molecular bonds with a single barrier are often observed. The Bell model is commonly used for the analysis of rupture force measurements with bonds displaying a single barrier. It provides an analytical expression of the most likely rupture force which makes it very simple to use. However, in principle, it can only be applied to landscapes with extrema whose positions do not vary under force. Here, we evaluate the general relevance of the Bell model by comparing it with another analytical model for which the landscape is harmonic in the vicinity of its extrema. Similar shapes of force distributions are obtained with both models, making it difficult to confirm the validity of the Bell model for a given set of experimental data. Nevertheless, we show that the analysis of rupture force experiments on such harmonic landscapes with the Bell model provides excellent results in most cases. However, numerical computation of the distributions of the rupture forces on piecewise-linear energy landscapes indicates that the blind use of any model such as the Bell model may be risky, since there often exist several landscapes compatible with a given set of experimental data. Finally, we derive a universal relation between the range and energy of the bond and the force spectrum. This relation does not depend on the shape of the energy landscape and can thus be used to characterize unambiguously any one-barrier landscape from experiments. All the results are illustrated with the streptavidin-biotin bond.

Entities:  

Year:  2008        PMID: 18352091     DOI: 10.1103/PhysRevE.77.026108

Source DB:  PubMed          Journal:  Phys Rev E Stat Nonlin Soft Matter Phys        ISSN: 1539-3755


  8 in total

1.  Long lifetime of hydrogen-bonded DNA basepairs by force spectroscopy.

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2.  Methods and estimations of uncertainties in single-molecule dynamic force spectroscopy.

Authors:  Oscar Björnham; Staffan Schedin
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3.  A nanomechanical interface to rapid single-molecule interactions.

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Journal:  Nat Commun       Date:  2011       Impact factor: 14.919

4.  Characterizing cell adhesion by using micropipette aspiration.

Authors:  Brenna Hogan; Avin Babataheri; Yongyun Hwang; Abdul I Barakat; Julien Husson
Journal:  Biophys J       Date:  2015-07-21       Impact factor: 4.033

5.  Fibers with integrated mechanochemical switches: minimalistic design principles derived from fibronectin.

Authors:  Orit Peleg; Thierry Savin; German V Kolmakov; Isaac G Salib; Anna C Balazs; Martin Kröger; Viola Vogel
Journal:  Biophys J       Date:  2012-11-07       Impact factor: 4.033

Review 6.  Mechanochemitry: a molecular biomechanics view of mechanosensing.

Authors:  Cheng Zhu
Journal:  Ann Biomed Eng       Date:  2013-09-05       Impact factor: 3.934

7.  Reconsideration of dynamic force spectroscopy analysis of streptavidin-biotin interactions.

Authors:  Atsushi Taninaka; Osamu Takeuchi; Hidemi Shigekawa
Journal:  Int J Mol Sci       Date:  2010-05-13       Impact factor: 5.923

8.  Force measurement enabling precise analysis by dynamic force spectroscopy.

Authors:  Atsushi Taninaka; Yuuichi Hirano; Osamu Takeuchi; Hidemi Shigekawa
Journal:  Int J Mol Sci       Date:  2011-12-29       Impact factor: 5.923

  8 in total

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