Detecting Molecular Folding from Noise Measurements

Author:

Rico-Pasto Marc1ORCID,Ritort Felix23ORCID

Affiliation:

1. Unit of Biophysics and Bioengineering, Department of Biomedicine, School of Medicine and Health Sciences, University of Barcelona, C/Casanoves 143, 08036 Barcelona, Spain

2. Small Small Biosystems Lab, Condensed Matter Physics Department, Physics School, University of Barcelona, C/Martí i Franquès 1, 08028 Barcelona, Spain

3. Institut de Nanociéncia i Nanotecnologia (IN2UB), University of Barcelona, 08028 Barcelona, Spain

Abstract

Detecting conformational transitions in molecular systems is key to understanding biological processes. Here, we investigate the force variance in single-molecule pulling experiments as an indicator of molecular folding transitions. We consider cases where Brownian force fluctuations are large, masking the force rips and jumps characteristics of conformational transitions. We compare unfolding and folding data for DNA hairpin systems of loop sizes 4, 8, and 20 and the 110-amino acid protein barnase, finding conditions that facilitate the detection of folding events at low forces where the signal-to-noise ratio is low. In particular, we discuss the role of temperature as a useful parameter to improve the detection of folding transitions in entropically driven processes where folding forces are temperature independent. The force variance approach might be extended to detect the elusive intermediate states in RNA and protein folding.

Funder

Spanish Research Council

Icrea Academia prize 2018

Publisher

MDPI AG

Subject

General Medicine

Reference27 articles.

1. Are there pathways for protein folding?;Levinthal;J. Chim. Phys.,1968

2. Molten Globule and Protein Folding;Ptitsyn;Adv. Protein Chem.,1995

3. Evidence for a molten globule-like transition state in protein folding from determination of activation volumes;Vidugiris;Biochemistry,1995

4. Role of the molten globule state in protein folding;Arai;Adv. Protein Chem.,2000

5. Study of the “molten globule” intermediate state in protein folding by a hydrophobic fluorescent probe;Semisotnov;Biopolym. Orig. Res. Biomol.,1991

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