The stability and number of nucleating interactions determine DNA hybridization rates in the absence of secondary structure

Author:

Hertel Sophie1,Spinney Richard E12,Xu Stephanie Y1,Ouldridge Thomas E3,Morris Richard G12,Lee Lawrence K14ORCID

Affiliation:

1. EMBL Australia Node for Single Molecule Science, School of Medical Sciences, University of New South Wales , Sydney  2052 ,  Australia

2. School of Physics, University of New South Wales, Sydney 2052 ,  Australia

3. Department of Bioengineering and Centre for Synthetic Biology , Imperial College London,  London  SW7 2AZ, UK

4. ARC Centre of Excellence in Synthetic Biology, University of New South Wales , Sydney, Australia

Abstract

AbstractThe kinetics of DNA hybridization are fundamental to biological processes and DNA-based technologies. However, the precise physical mechanisms that determine why different DNA sequences hybridize at different rates are not well understood. Secondary structure is one predictable factor that influences hybridization rates but is not sufficient on its own to fully explain the observed sequence-dependent variance. In this context, we measured hybridization rates of 43 different DNA sequences that are not predicted to form secondary structure and present a parsimonious physically justified model to quantify our observations. Accounting only for the combinatorics of complementary nucleating interactions and their sequence-dependent stability, the model achieves good correlation with experiment with only two free parameters. Our results indicate that greater repetition of Watson–Crick pairs increases the number of initial states able to proceed to full hybridization, with the stability of those pairings dictating the likelihood of such progression, thus providing new insight into the physical factors underpinning DNA hybridization rates.

Funder

Australian Research Council

National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Genetics

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