Displacement and dissociation of oligonucleotides during DNA hairpin closure under strain

Author:

Ding Fangyuan123ORCID,Cocco Simona4,Raj Saurabh5,Manosas Maria67,Nguyen Thao Thi Thu2,Spiering Michelle M8,Bensimon David4910,Allemand Jean-François49,Croquette Vincent4911

Affiliation:

1. Department of Biomedical Engineering, University of California , Irvine , CA 92617 , USA

2. Center for Complex Biological Systems, University of California , Irvine , CA 92697 , USA

3. Center for Synthetic Biology, Chao Family Comprehensive Cancer Center, Department of Developmental and Cell Biology, and Department of Pharmaceutical Sciences, University of California , Irvine , CA 92697 , USA

4. Laboratoire de Physique de l’Ecole normale supérieure, ENS, Université PSL, CNRS, Sorbonne Université, Université Paris Cité , Paris , France

5. Kusuma School of Biological Sciences, Indian Institute of Technology , Delhi , 110016 , India

6. Small Biosystems Lab, Departament de Física de la Matèria Condensada, Facultat de Física, Universitat de Barcelona , Carrer de Martí i Franquès, 1 , 08028 Barcelona , Spain

7. Institut de Nanociència i Nanotecnologia (IN2UB), Universitat de Barcelona , 08028 Barcelona, Spain

8. Department of Chemistry, The Pennsylvania State University, University Park , PA  16802,  USA

9. Institut de Biologie de l’École Normale Supérieure (IBENS), CNRS, Inserm, École Normale Supérieure, PSL Research University , F-75005 , Paris , France

10. Department of Chemistry and Biochemistry, University of California Los Angeles , Los Angeles , CA  90095,  USA

11. ESPCI Paris, Université PSL , Paris , France

Abstract

Abstract The hybridization kinetic of an oligonucleotide to its template is a fundamental step in many biological processes such as replication arrest, CRISPR recognition, DNA sequencing, DNA origami, etc. Although single kinetic descriptions exist for special cases of this problem, there are no simple general prediction schemes. In this work, we have measured experimentally, with no fluorescent labelling, the displacement of an oligonucleotide from its substrate in two situations: one corresponding to oligonucleotide binding/unbinding on ssDNA and one in which the oligonucleotide is displaced by the refolding of a dsDNA fork. In this second situation, the fork is expelling the oligonucleotide thus significantly reducing its residence time. To account for our data in these two situations, we have constructed a mathematical model, based on the known nearest neighbour dinucleotide free energies, and provided a good estimate of the residence times of different oligonucleotides (DNA, RNA, LNA) of various lengths in different experimental conditions (force, temperature, buffer conditions, presence of mismatches, etc.). This study provides a foundation for the dynamics of oligonucleotide displacement, a process of importance in numerous biological and bioengineering contexts.

Funder

Schlumberger Foundation

ERC

Human Frontier Science Program

Fondation Pierre-Gilles de Gennes

Centre National de la Recherche Scientifique

Spanish Research Council

MICINN

NIH Director's New Innovator Award

University of California-Irvine

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference51 articles.

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