Article

Theoretical study of sequence-dependent nanopore unzipping of DNA.

Nanobiophysique, Ecole Superieure Physique et Chimie Industrielles, Centre National de Recherche Scientifique, Paris, France.
Biophysical Journal (impact factor: 3.65). 05/2008; 94(7):2716-24. DOI:10.1529/biophysj.107.111732 pp.2716-24
Source: PubMed

ABSTRACT We theoretically investigate the unzipping of DNA electrically driven through a nanometer-size pore. Taking the DNA base sequence explicitly into account, the unpairing and translocation process is described by a biased random walk in a one-dimensional energy landscape determined by the sequential basepair opening. Distributions of translocation times are numerically calculated as a function of applied voltage and temperature. We show that varying these two parameters changes the dynamics from a predominantly diffusive behavior to a dynamics governed by jumps over local energy barriers. The work suggests experimentally studying sequence effects, by comparing the average value and standard deviation of the statistical distribution of translocation times.

0 0
 · 
0 Bookmarks
 · 
20 Views
  • Source
    Article: Translocation of structured polynucleotides through nanopores.
    [show abstract] [hide abstract]
    ABSTRACT: We investigate theoretically the translocation of structured RNA/DNA molecules through narrow pores which allow single but not double strands to pass. The unzipping of basepaired regions within the molecules presents significant kinetic barriers for the translocation process. We show that this circumstance may be exploited to determine the full basepairing pattern of polynucleotides, including RNA pseudoknots. The crucial requirement is that the translocation dynamics (i.e. the length of the translocated molecular segment) needs to be recorded as a function of time with a spatial resolution of a few nucleotides. This could be achieved, for instance, by applying a mechanical driving force for translocation and recording force-extension curves (FECs) with a device such as an atomic force microscope or optical tweezers. Our analysis suggests that, with this added spatial resolution, nanopores could be transformed into a powerful experimental tool to study the folding of nucleic acids.
    Physical Biology 07/2004; 1(1-2):19-26. · 2.60 Impact Factor
  • Source
    Article: Slow nucleic acid unzipping kinetics from sequence-defined barriers.
    [show abstract] [hide abstract]
    ABSTRACT: Recent experiments on unzipping of RNA helix-loop structures by force have shown that approximately 40-base molecules can undergo kinetic transitions between two well-defined "open" and "closed" states, on a timescale approximately 1 sec [Liphardt et al., Science 297, 733-737 (2001)]. Using a simple dynamical model, we show that these phenomena result from the slow kinetics of crossing large free energy barriers which separate the open and closed conformations. The dependence of barriers on sequence along the helix, and on the size of the loop(s) is analyzed. Some DNA and RNA sequences that could show dynamics on different time scales, or three(or more)-state unzipping, are proposed. Our dynamical model is also applied to the unzipping of long (kilo-basepair) DNA molecules at constant force.
    The European Physical Journal E 03/2003; 10(2):153-61. · 1.94 Impact Factor

Keywords

biased random walk
 
diffusive behavior
 
Distributions
 
DNA base sequence
 
DNA electrically
 
dynamics
 
one-dimensional energy landscape
 
statistical distribution
 
translocation process
 
two parameters changes
 
unpairing
 

U Bockelmann