Literature DB >> 29385343

Two-State Folding Energy Determination Based on Transition Points in Nonequilibrium Single-Molecule Experiments.

Huijuan You1,2, Shiwen Guo2, Shimin Le3, Qingnan Tang3, Mingxi Yao2, Xiaodan Zhao2, Jie Yan2,3,4.   

Abstract

Many small protein domains or nucleic acid structures undergo two-state unfolding-refolding transitions during mechanical stretching using single-molecule techniques. Here, by applying the Jarzynski equality (JE), we analytically express the folding energy of a molecule as a function of the experimentally measured transition points ξ* obtained with two typical time-varying mechanical constraints: the force constraints F(t) and the position constraints R(t) of a Hookian spring attached to one end of the molecule. Compared to previous applications of JE based on the integration of accurately measured force-extension curves of a tether that typically contains the molecule of interest and handles, our approach just needs to accurately measure a single data point. In the case of the F(t) process, the calculation is handle-independent. The broad applications of the theory are demonstrated by measuring the folding energies of a DNA hairpin, a DNA G-quadruplex, and the titin I27 domain based on transition forces using magnetic tweezers.

Year:  2018        PMID: 29385343     DOI: 10.1021/acs.jpclett.7b03123

Source DB:  PubMed          Journal:  J Phys Chem Lett        ISSN: 1948-7185            Impact factor:   6.475


  2 in total

Review 1.  Characterization of G-Quadruplexes Folding/Unfolding Dynamics and Interactions with Proteins from Single-Molecule Force Spectroscopy.

Authors:  Yuanlei Cheng; Yashuo Zhang; Huijuan You
Journal:  Biomolecules       Date:  2021-10-25

2.  Structural-elastic determination of the force-dependent transition rate of biomolecules.

Authors:  Shiwen Guo; Qingnan Tang; Mingxi Yao; Huijuan You; Shimin Le; Hu Chen; Jie Yan
Journal:  Chem Sci       Date:  2018-05-29       Impact factor: 9.825

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.