Ripping RNA by Force Using Gaussian Network Models
Author(s) -
Changbong Hyeon,
D. Thirumalai
Publication year - 2016
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.6b09402
Subject(s) - ribozyme , rna , gaussian network model , isotropy , optical tweezers , hairpin ribozyme , physics , context (archaeology) , gaussian , topology (electrical circuits) , folding (dsp implementation) , statistical physics , biophysics , biological system , chemistry , biology , mathematics , quantum mechanics , engineering , paleontology , biochemistry , combinatorics , gene , electrical engineering
Using force as a probe to map the folding landscapes of RNA molecules has become a reality thanks to major advances in single molecule pulling experiments. Although the unfolding pathways under tension are complicated to predict, studies in the context of proteins have shown that topology is the major determinant of the unfolding landscapes. By building on this finding we study the responses of RNA molecules to force by adapting Gaussian network model (GNM) that represents RNAs using a bead-spring network with isotropic interactions. Cross-correlation matrices of residue fluctuations, which are analytically calculated using GNM even upon application of mechanical force, show distinct allosteric communication as RNAs rupture. The model is used to calculate the force-extension curves at full thermodynamic equilibrium, and the corresponding unfolding pathways of four RNA molecules subject to a quasi-statically increased force. Our study finds that the analysis using GNM captures qualitatively the unfolding pathway of T. ribozyme elucidated by the optical tweezers measurement. However, the simple model cannot capture features, such as bifurcation in the unfolding pathways or the ion effects, in the forced-unfolding of RNAs.
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