Single molecule statistics and the polynucleotide unzipping transition

Lubensky, David K.; Nelson, David R.

doi:10.1103/physreve.65.031917

Cited by 158 publications

(190 citation statements)

References 79 publications

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“…Sequence heterogeneity leads to models with elastic "disorder", which could dramatically alter the physics of shear unzipping, as found earlier for tensile unzipping [8,9]. We note that inchworm excitations, which exploit translational invariance, [20] and are neglected here, are strongly disfavored by sequence heterogeneity.…”

Section: Discussionsupporting

confidence: 60%

Shear Unzipping of DNA

Chakrabarti

Nelson

2009

J. Phys. Chem. B

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We study theoretically the mechanical failure of a simple model of double stranded DNA under an applied shear. Starting from a more microscopic Hamiltonian that describes a sheared DNA, we arrive at a nonlinear generalization of a ladder model of shear unzipping proposed earlier by deGennes [1]. Using this model and a combination of analytical and numerical methods, we study the DNA "unzipping" transition when the shearing force exceeds a critical threshold at zero temperature. We also explore the effects of sequence heterogeneity and finite temperature and discuss possible applications to determine the strength of colloidal nanoparticle assemblies functionalized by DNA.

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Section: Discussionsupporting

confidence: 60%

Shear Unzipping of DNA

Chakrabarti

Nelson

2009

J. Phys. Chem. B

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“…For each hairpin construct, we made a quantitative model of the folding landscape, adapting elements from previous models for dsDNA stretching (33) and unzipping (34) and RNA unfolding (27,21,35,36). This model incorporates five distinct components: the energetic contributions arising from (i) base stacking and hydrogen bonding within the folded helix, (ii) stretching of the ssDNA liberated by the hairpin unfolding, and (iii) molecular motions in the optical trap; and the effects of elastic compliance associated with (iv) the ssDNA of the unfolded state and (v) the dsDNA handles attached to the hairpin.…”

Section: Resultsmentioning

confidence: 99%

Nanomechanical measurements of the sequence-dependent folding landscapes of single nucleic acid hairpins

Woodside

Behnke-Parks²,

Larizadeh³

et al. 2006

Proc. Natl. Acad. Sci. U.S.A.

444

556

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Nucleic acid hairpins provide a powerful model system for probing the formation of secondary structure. We report a systematic study of the kinetics and thermodynamics of the folding transition for individual DNA hairpins of varying stem length, loop length, and stem GC content. Folding was induced mechanically in a highresolution optical trap using a unique force clamp arrangement with fast response times. We measured 20 different hairpin sequences with quasi-random stem sequences that were 6 -30 bp long, polythymidine loops that were 3-30 nt long, and stem GC content that ranged from 0% to 100%. For all hairpins studied, folding and unfolding were characterized by a single transition. From the force dependence of these rates, we determined the position and height of the energy barrier, finding that the transition state for duplex formation involves the formation of 1-2 bp next to the loop. By measuring unfolding energies spanning one order of magnitude, transition rates covering six orders of magnitude, and hairpin opening distances with subnanometer precision, our results define the essential features of the energy landscape for folding. We find quantitative agreement over the entire range of measurements with a hybrid landscape model that combines thermodynamic nearest-neighbor free energies and nanomechanical DNA stretching energies.DNA hairpin ͉ energy landscape ͉ force clamp ͉ optical tweezers ͉ single molecule H airpins formed from self-complementary sequences supply a model system for studying folding and duplex formation, the most fundamental processes for generating structure in nucleic acids. Using hairpins, repeated measurements can be made on the same molecule, facilitating single-molecule studies. Furthermore, by simply altering the nucleotide sequence, physical properties such as folding energies, kinetic rates, and distances to transition states all can be changed systematically. Hairpins also play essential roles in vivo. DNA hairpins bind proteins to regulate transcription (1), and hairpin intermediates are involved in both replication and recombination (2, 3). RNA hairpins form tertiary contacts (4), bind to proteins (2), regulate transcription (5), and mediate RNA interference (6). Understanding the factors that influence hairpin folding should therefore not only elucidate principles of structure formation in nucleic acids but may also shed light on the biological roles played by these structures.Extensive calorimetric and melting studies have been carried out to generate predictive rules for the thermodynamic stability of arbitrary nucleic acid duplexes (7). The kinetic properties of duplex formation, however, remain less well understood, particularly those related to the nature of the transition state. Temperature-jump studies of annealing in short duplexes have been interpreted in terms of the nucleation of a transition state consisting of Ϸ1-3 bp, followed by zippering of the remaining stem (8). This interpretation, however, rests on the assumption that the enthalpy of activation arises ...

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“…Lubensky and Nelson [1091,1092] have studied a class of micromanipulation experiments, exemplified by the pulling apart of the two strands of double-stranded DNA. When the pulling force is increased to a critical value, an ''unzipping'' or ''unravelling'' transition occurs.…”

Section: Molecule Stretchingmentioning

confidence: 99%