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Transition state theory demonstrated at the micron scale with out-of-equilibrium transport in a confined environment

TLDR
This work applies transition state theory to out-of-equilibrium transport through confined environments: the thermally activated translocation of single DNA molecules over an entropic barrier helped by an external force field.
Abstract
Transition state theory (TST) provides a simple interpretation of many thermally activated processes. It applies successfully on timescales and length scales that differ several orders of magnitude: to chemical reactions, breaking of chemical bonds, unfolding of proteins and RNA structures and polymers crossing entropic barriers. Here we apply TST to out-of-equilibrium transport through confined environments: the thermally activated translocation of single DNA molecules over an entropic barrier helped by an external force field. Reaction pathways are effectively one dimensional and so long that they are observable in a microscope. Reaction rates are so slow that transitions are recorded on video. We find sharp transition states that are independent of the applied force, similar to chemical bond rupture, as well as transition states that change location on the reaction pathway with the strength of the applied force. The states of equilibrium and transition are separated by micrometres as compared with angstroms/nanometres for chemical bonds.

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Citations
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Probing the organization and dynamics of two DNA chains trapped in a nanofluidic cavity

TL;DR: A pneumatically-actuated nanofluidic platform that has the capability of dynamically controlling the confinement environment of macromolecules in solution is presented, using pneumatic pressure to deflect a thin nitride lid into a nanoslit, confining molecules in an array of cavities embedded in the slit.
Journal ArticleDOI

Evolution of Nested Folding States in Compression of a Strongly Confined Semiflexible Chain

TL;DR: In this article, a gasket translating at a fixed sliding speed impinges on a nanochannel extended chain and a unique folding kinetics driven by repeated double-fold nucleation events and growth of nested folds is investigated.
Journal ArticleDOI

Waves of DNA: Propagating excitations in extended nanoconfined polymers.

TL;DR: In this article, a single DNA molecule is confined in a nanofluidic slit etched with arrays of embedded nanocavities; the cavity lattice is designed so that a single chain occupies multiple cavities.
Journal ArticleDOI

Modeling in food across the scales: towards a universal mass transfer simulator of small molecules in food

TL;DR: In this paper, a special implementation of Langevin dynamics is proposed to describe mass transfer in structured food, where the concepts of random walks over discrete times and physicochemical interactions are connected via an exact solution of the Fokker-Planck equation across interfaces.
Journal ArticleDOI

Concentrating and labeling genomic DNA in a nanofluidic array

TL;DR: A device and a protocol for the enzymatic labeling of genomic DNA arranged in a dense array of single molecules without attaching the enzyme or the DNA to a surface is demonstrated and may be an important preparative module for carrying out enzymatics processing on DNA extracted from single-cells in a microfluidic chip.
References
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Journal ArticleDOI

Brownian motion in a field of force and the diffusion model of chemical reactions

TL;DR: In this article, a particle which is caught in a potential hole and which, through the shuttling action of Brownian motion, can escape over a potential barrier yields a suitable model for elucidating the applicability of the transition state method for calculating the rate of chemical reactions.
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Models for the specific adhesion of cells to cells

TL;DR: The force required to separate two cells is shown to be greater than the expected electrical forces between cells, and of the same order of magnitude as the forces required to pull gangliosides and perhaps some integral membrane proteins out of the cell membrane.
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Probing the Relation Between Force—Lifetime—and Chemistry in Single Molecular Bonds

TL;DR: The method of dynamic force spectroscopy (DFS) is being used to probe the complex relation between force-lifetime-and chemistry in single molecular bonds, and probes the inner world of molecular interactions to reveal barriers that are difficult or impossible to detect in assays of near equilibrium dissociation but that determine bond lifetime and strength under rapid detachment.
Journal ArticleDOI

Intrinsic rates and activation free energies from single-molecule pulling experiments.

TL;DR: By analyzing simulated data, it is shown that the resulting rates of force-induced rupture are significantly more reliable than those obtained by the widely used approach based on Bell's formula.
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