322 research outputs found
A charged particle in a magnetic field - Jarzynski Equality
We describe some solvable models which illustrate the Jarzynski theorem and
related fluctuation theorems. We consider a charged particle in the presence of
magnetic field in a two dimensional harmonic well. In the first case the centre
of the harmonic potential is translated with a uniform velocity, while in the
other case the particle is subjected to an ac force. We show that Jarzynski
identity complements Bohr-van Leeuwen theorem on the absence of diamagnetism in
equilibrium classical system.Comment: 5 pages, minor corrections made and journal reference adde
Single molecule experiments in biophysics: exploring the thermal behavior of nonequilibrium small systems
Biomolecules carry out very specialized tasks inside the cell where energies
involved are few tens of k_BT, small enough for thermal fluctuations to be
relevant in many biomolecular processes. In this paper I discuss a few concepts
and present some experimental results that show how the study of fluctuation
theorems applied to biomolecules contributes to our understanding of the
nonequilibrium thermal behavior of small systems.Comment: Proceedings of the 22nd Statphys Conference 2004 (Bangalore,India).
Invited contributio
Phase diagram for unzipping DNA with long-range interactions
We present a critique and extension of the mean-field approach to the
mechanical pulling transition in bound polymer systems. Our model is motivated
by the theoretically and experimentally important examples of adsorbed polymers
and double-stranded DNA, and we focus on the case in which quenched disorder in
the sequence of monomers is unimportant for the statistical mechanics. We show
how including excluded volume interactions in the model affects the phase
diagram for the critical pulling force, and we predict a re-entrancy phase at
low temperatures which has not been previously discussed. We also consider the
case of non-equilibrium pulling, in which the external force probes the local,
rather than the global structure of the dsDNA or adsorbed polymer. The dynamics
of the pulling transition in such experiments could illuminate the polymer's
loop structure, which depends on the nature of excluded volume interactions.Comment: 4 pages, 2 figures; this version clarifies Eq. 8, and corrects errors
in Fig.
Inferring DNA sequences from mechanical unzipping data: the large-bandwidth case
The complementary strands of DNA molecules can be separated when stretched
apart by a force; the unzipping signal is correlated to the base content of the
sequence but is affected by thermal and instrumental noise. We consider here
the ideal case where opening events are known to a very good time resolution
(very large bandwidth), and study how the sequence can be reconstructed from
the unzipping data. Our approach relies on the use of statistical Bayesian
inference and of Viterbi decoding algorithm. Performances are studied
numerically on Monte Carlo generated data, and analytically. We show how
multiple unzippings of the same molecule may be exploited to improve the
quality of the prediction, and calculate analytically the number of required
unzippings as a function of the bandwidth, the sequence content, the elasticity
parameters of the unzipped strands
Two enzymes catalyze vitamin K 2,3-epoxide reductase activity in mouse: VKORC1 is highly expressed in exocrine tissues while VKORC1L1 is highly expressed in brain
AbstractVKORC1 and VKORC1L1 are enzymes that both catalyze the reduction of vitamin K2,3-epoxide via vitamin K quinone to vitamin K hydroquinone. VKORC1 is the key enzyme of the classical vitamin K cycle by which vitamin K-dependent (VKD) proteins are Îł-carboxylated by the hepatic Îł-glutamyl carboxylase (GGCX). In contrast, the VKORC1 paralog enzyme, VKORC1L1, is chiefly responsible for antioxidative function by reduction of vitamin K to prevent damage by intracellular reactive oxygen species. To investigate tissue-specific vitamin K 2,3-epoxide reductase (VKOR) function of both enzymes, we quantified mRNA levels for VKORC1, VKORC1L1, GGCX, and NQO1 and measured VKOR enzymatic activities in 29 different mouse tissues. VKORC1 and GGCX are highly expressed in liver, lung and exocrine tissues including mammary gland, salivary gland and prostate suggesting important extrahepatic roles for the vitamin K cycle. Interestingly, VKORC1L1 showed highest transcription levels in brain. Due to the absence of detectable NQO1 transcription in liver, we assume this enzyme has no bypass function with respect to activation of VKD coagulation proteins. Our data strongly suggest diverse functions for the vitamin K cycle in extrahepatic biological pathways
A quantum version of free energy - irreversible work relations
We give a quantum version of the Jarzynski relation between the distribution
of work done over a certain time-interval on a system and the difference of
equilibrium free energies. The main new ingredient is the identification of
work depending on the quantum history of the system and the proper definition
of various quantum ensembles over which the averages should be made. We also
discuss a number of different regimes that have been considered by other
authors and which are unified in the present set-up. In all cases, and quantum
or classical, it is a general relation between heat and time-reversal that
makes the Jarzynski relation so universally valid
Probing complex RNA structures by mechanical force
RNA secondary structures of increasing complexity are probed combining single
molecule stretching experiments and stochastic unfolding/refolding simulations.
We find that force-induced unfolding pathways cannot usually be interpretated
by solely invoking successive openings of native helices. Indeed, typical
force-extension responses of complex RNA molecules are largely shaped by
stretching-induced, long-lived intermediates including non-native helices. This
is first shown for a set of generic structural motifs found in larger RNA
structures, and then for Escherichia coli's 1540-base long 16S ribosomal RNA,
which exhibits a surprisingly well-structured and reproducible unfolding
pathway under mechanical stretching. Using out-of-equilibrium stochastic
simulations, we demonstrate that these experimental results reflect the slow
relaxation of RNA structural rearrangements. Hence, micromanipulations of
single RNA molecules probe both their native structures and long-lived
intermediates, so-called "kinetic traps", thereby capturing -at the single
molecular level- the hallmark of RNA folding/unfolding dynamics.Comment: 9 pages, 9 figure
Nanowire assembly, e.g. for optical probes, comprises optically trapping high aspect ratio semiconductor nanowire with infrared single-beam optical trap and attaching nanowire to organic or inorganic structure
NOVELTY - A nanowire assembly method comprises optically trapping a semiconductor nanowire with an infrared single-beam optical trap and attaching the nanowire to an organic or inorganic structure by laser fusing. The nanowire is further trapped in a fluid environment. The optical trap has a beam wavelength of 1064 nm. The nanowire has an aspect ratio greater than 100 and a diameter less than 100 (preferably less than 80) nm. The nanowire and the organic or inorganic structure form a heterostructure. USE - For fabricating a nanowire assembly for use as e.g. active photonic devices, passive photonic devices, optical probes, subwavelength microscopy. ADVANTAGE - Nanowires with diameters as small as 20 nm and aspect ratios of above one hundred can be trapped and transported in three dimensions, enabling the construction of nanowire architectures which may function in various capacities. Nanowire structures can now be assembled in physiological environments, offering new forms of chemical, mechanical and optical stimulation of living cells. DETAILED DESCRIPTION - An INDEPENDENT CLAIM is included for a nanowire assembly comprising a nanowire and an organic or inorganic structure or an arbitrary structure. DESCRIPTION OF DRAWING(S) - The figure shows a schematic diagram of an optical tweezers instrument for nanowire trapping
Extracting Structural Information of a Heteropolymer from Force-Extension Curves
We present a theory for the reverse analysis on the sequence information of a
single H/P two-letter random hetero-polymer (RHP) from its force-extension(f-z)
curves during quasi static stretching. Upon stretching of a self-assembled RHP,
it undergoes several structural transitions. The typical elastic response of a
hetero-polymeric globule is a set of overlapping saw-tooth patterns. With
consideration of the height and the position of the overlapping saw-tooth
shape, we analyze the possibility of extracting the binding energies of the
internal domains and the corresponding block sizes of the contributing
conformations.Comment: 5 figures 7 page
Fabrication of 10 nm diameter hydrocarbon nanopores
The addition of carbon to samples, during transmission electron microscope imaging, presents a barrier to accurate analysis; the controlled deposition of hydrocarbons by a focused electron beam can be a useful technique for local nanometer-scale sculpting of material. Here we use hydrocarbon deposition to form nanopores from larger focused ion beam holes in silicon nitride membranes. Using this method, we close 100–200 nm diameter holes to diameters of 10 nm and below, with deposition rates of 0.6 nm/min. I-V characteristics of electrolytic flow through these nanopores agree quantitatively with a one dimensional model at all examined salt concentrations
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