2,455 research outputs found
Critical voltage of a mesoscopic superconductor
We study the role of the quasiparticle distribution function f on the
properties of a superconducting nanowire. We employ a numerical calculation
based upon the Usadel equation. Going beyond linear response, we find a
non-thermal distribution for f caused by an applied bias voltage. We
demonstrate that the even part of f (the energy mode f_L) drives a first order
transition from the superconducting state to the normal state irrespective of
the current
Highly Non-linear Excitonic Zeeman Spin-Splitting in Composition-Engineered Artificial Atoms
Non-linear Zeeman splitting of neutral excitons is observed in composition
engineered In(x)Ga(1-x)As self-assembled quantum dots and its microscopic
origin is explained. Eight-band k.p simulations, performed using realistic dot
parameters extracted from cross-sectional scanning tunneling microscopy, reveal
that a quadratic contribution to the Zeeman energy originates from a spin
dependent mixing of heavy and light hole orbital states in the dot. The dilute
In-composition (x<0.35) and large lateral size (40-50 nm) of the quantum dots
investigated is shown to strongly enhance the non-linear excitonic Zeeman gap,
providing a blueprint to enhance such magnetic non-linearities via growth
engineering
Strong electrically tunable exciton g-factors in an individual quantum dots due to hole orbital angular momentum quenching
Strong electrically tunable exciton g-factors are observed in individual
(Ga)InAs self-assembled quantum dots and the microscopic origin of the effect
is explained. Realistic eight band k.p simulations quantitatively account for
our observations, simultaneously reproducing the exciton transition energy, DC
Stark shift, diamagnetic shift and g-factor tunability for model dots with the
measured size and a comparatively low In-composition of x(In)~35% near the dot
apex. We show that the observed g-factor tunability is dominated by the hole,
the electron contributing only weakly. The electric field induced perturbation
of the hole wavefunction is shown to impact upon the g-factor via orbital
angular momentum quenching, the change of the In:Ga composition inside the
envelope function playing only a minor role. Our results provide design rules
for growing self-assembled quantum dots for electrical spin manipulation via
electrical g-factor modulation
Accumulation of properly folded human type III procollagen molecules in specific intracellular membranous compartments in the yeast Pichia pastoris
It was recently reported that co-expression of the proal(III) chain of human type III procollagen with the subunits of human prolyl 4-hydroxylase in Pichia pastoris produces fully hydroxylated and properly folded recombinant type III procollagen molecules (Vuorela, A., Myllyharju, J., Nissi, R., Pihlajaniemi, T., Kivirikko, K.I., 1997. Assembly of human prolyl 4-hydroxylase and type III collagen in the yeast Pichia pastoris: formation of a stable enzyme tetramer requires coexpression with collagen and assembly of a stable collagen requires coexpression with prolyl 4-hydroxylase. EMBO J, 16, 6702-6712). These properly folded molecules accumulated inside the yeast cell, however, only similar to 10% were found in the culture medium. We report here that replacement of the authentic signal sequence of the human pro alpha 1(III) with the Saccharomyces cerevisiae alpha mating factor prepro sequence led only to a minor increase in the amount secreted. Immunoelectron microscopy studies indicated that the procollagen molecules accumulate in specific membranous vesicular compartments that are closely associated with the nuclear membrane. Prolyl 4-hydroxylase, an endoplasmic reticulum (ER) lumenal enzyme, was found to be located in the same compartments. Non-helical pro alpha 1(III) chains produced by expression without recombinant prolyl 4-hydroxylase likewise accumulated within these compartments, The data indicate that properly folded recombinant procollagen molecules accumulate within the ER and do not proceed further in the secretory pathway. This may be related to the large size of the procollagen molecule. (C) 2000 Elsevier Science B.V./International Society of Matrix Biology. All rights reserved
Efficient Reactive Brownian Dynamics
We develop a Split Reactive Brownian Dynamics (SRBD) algorithm for particle
simulations of reaction-diffusion systems based on the Doi or volume reactivity
model, in which pairs of particles react with a specified Poisson rate if they
are closer than a chosen reactive distance. In our Doi model, we ensure that
the microscopic reaction rules for various association and disassociation
reactions are consistent with detailed balance (time reversibility) at
thermodynamic equilibrium. The SRBD algorithm uses Strang splitting in time to
separate reaction and diffusion, and solves both the diffusion-only and
reaction-only subproblems exactly, even at high packing densities. To
efficiently process reactions without uncontrolled approximations, SRBD employs
an event-driven algorithm that processes reactions in a time-ordered sequence
over the duration of the time step. A grid of cells with size larger than all
of the reactive distances is used to schedule and process the reactions, but
unlike traditional grid-based methods such as Reaction-Diffusion Master
Equation (RDME) algorithms, the results of SRBD are statistically independent
of the size of the grid used to accelerate the processing of reactions. We use
the SRBD algorithm to compute the effective macroscopic reaction rate for both
reaction- and diffusion-limited irreversible association in three dimensions.
We also study long-time tails in the time correlation functions for reversible
association at thermodynamic equilibrium. Finally, we compare different
particle and continuum methods on a model exhibiting a Turing-like instability
and pattern formation. We find that for models in which particles diffuse off
lattice, such as the Doi model, reactions lead to a spurious enhancement of the
effective diffusion coefficients.Comment: To appear in J. Chem. Phy
Shape control of QDs studied by cross-sectional scanning tunneling microscopy
In this cross-sectional scanning tunneling microscopy study we investigated
various techniques to control the shape of self-assembled quantum dots (QDs)
and wetting layers (WLs). The result shows that application of an indium flush
during the growth of strained InGaAs/GaAs QD layers results in flattened QDs
and a reduced WL. The height of the QDs and WLs could be controlled by varying
the thickness of the first capping layer. Concerning the technique of antimony
capping we show that the surfactant properties of Sb result in the preservation
of the shape of strained InAs/InP QDs during overgrowth. This could be achieved
by both a growth interrupt under Sb flux and capping with a thin GaAsSb layer
prior to overgrowth of the uncapped QDs. The technique of droplet epitaxy was
investigated by a structural analysis of strain free GaAs/AlGaAs QDs. We show
that the QDs have a Gaussian shape, that the WL is less than 1 bilayer thick,
and that minor intermixing of Al with the QDs takes place.Comment: 7 pages, 10 figure
Accumulation of properly folded human type III procollagen molecules in specific intracellular membranous compartments in the yeast Pichia pastoris
It was recently reported that co-expression of the proal(III) chain of human type III procollagen with the subunits of human prolyl 4-hydroxylase in Pichia pastoris produces fully hydroxylated and properly folded recombinant type III procollagen molecules (Vuorela, A., Myllyharju, J., Nissi, R., Pihlajaniemi, T., Kivirikko, K.I., 1997. Assembly of human prolyl 4-hydroxylase and type III collagen in the yeast Pichia pastoris: formation of a stable enzyme tetramer requires coexpression with collagen and assembly of a stable collagen requires coexpression with prolyl 4-hydroxylase. EMBO J, 16, 6702-6712). These properly folded molecules accumulated inside the yeast cell, however, only similar to 10% were found in the culture medium. We report here that replacement of the authentic signal sequence of the human pro alpha 1(III) with the Saccharomyces cerevisiae alpha mating factor prepro sequence led only to a minor increase in the amount secreted. Immunoelectron microscopy studies indicated that the procollagen molecules accumulate in specific membranous vesicular compartments that are closely associated with the nuclear membrane. Prolyl 4-hydroxylase, an endoplasmic reticulum (ER) lumenal enzyme, was found to be located in the same compartments. Non-helical pro alpha 1(III) chains produced by expression without recombinant prolyl 4-hydroxylase likewise accumulated within these compartments, The data indicate that properly folded recombinant procollagen molecules accumulate within the ER and do not proceed further in the secretory pathway. This may be related to the large size of the procollagen molecule. (C) 2000 Elsevier Science B.V./International Society of Matrix Biology. All rights reserved.</p
Shape control of QDs studied by cross-sectional scanning tunneling microscopy
In this cross-sectional scanning tunneling microscopy study we investigated
various techniques to control the shape of self-assembled quantum dots (QDs)
and wetting layers (WLs). The result shows that application of an indium flush
during the growth of strained InGaAs/GaAs QD layers results in flattened QDs
and a reduced WL. The height of the QDs and WLs could be controlled by varying
the thickness of the first capping layer. Concerning the technique of antimony
capping we show that the surfactant properties of Sb result in the preservation
of the shape of strained InAs/InP QDs during overgrowth. This could be achieved
by both a growth interrupt under Sb flux and capping with a thin GaAsSb layer
prior to overgrowth of the uncapped QDs. The technique of droplet epitaxy was
investigated by a structural analysis of strain free GaAs/AlGaAs QDs. We show
that the QDs have a Gaussian shape, that the WL is less than 1 bilayer thick,
and that minor intermixing of Al with the QDs takes place.Comment: 7 pages, 10 figure
The educational gradient of nonmarital childbearing in Europe:emergence of a pattern of disadvantage?
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