2,794 research outputs found
Ground-state clusters of two-, three- and four-dimensional +-J Ising spin glasses
A huge number of independent true ground-state configurations is calculated
for two-, three- and four-dimensional +- J spin-glass models. Using the genetic
cluster-exact approximation method, system sizes up to N=20^2,8^3,6^4 spins are
treated. A ``ballistic-search'' algorithm is applied which allows even for
large system sizes to identify clusters of ground states which are connected by
chains of zero-energy flips of spins. The number of clusters n_C diverges with
N going to infinity. For all dimensions considered here, an exponential
increase of n_C appears to be more likely than a growth with a power of N. The
number of different ground states is found to grow clearly exponentially with
N. A zero-temperature entropy per spin of s_0=0.078(5)k_B (2d), s_0=0.051(3)k_B
(3d) respectively s_0=0.027(5)k_B (4d) is obtained.Comment: large extensions, now 12 pages, 9 figures, 27 reference
Efficient Synthesis of Fluorescent Coumarins and Phosphorous-Containing Coumarin-Type Heterocycles via Palladium Catalyzed Cross-Coupling Reactions
Quantum-chemical calculations on the spectral properties of some aryl substituted 3-
phosphonocoumarins were performed, and the effect of the substituents in the aryl moiety was
evaluated. The structures possessing promising fluorescent properties were successfully synthesized via Suzuki and Sonogashira cross-coupling. The synthetic protocol was also applied for the
phosphorous chemoisomer of 3-phosphonocoumarin, 1,2-benzoxaphosphorin, and their carboxylate
analogues. The optical properties of the arylated and alkynylated products were experimentally
determined. The obtained quantum-chemical and experimental results give the possibility for a
fine tuning of the optical properties of phosphorous-containing coumarin systems by altering the
substituent at its C-6 position
Evolution of genes and repeats in the Nimrod superfamily
The recently identified Nimrod superfamily is characterized by the presence of a special type of EGF repeat, the NIM repeat, located right after a typical CCXGY/W amino acid motif. On the basis of structural features, nimrod genes can be divided into three types. The proteins encoded by Draper-type genes have an EMI domain at the N-terminal part and only one copy of the NIM motif, followed by a variable number of EGF-like repeats. The products of Nimrod B-type and Nimrod C-type genes (including the eater gene) have different kinds of N-terminal domains, and lack EGF-like repeats but contain a variable number of NIM repeats. Draper and Nimrod C-type (but not Nimrod B-type) proteins carry a transmembrane domain. Several members of the superfamily were claimed to function as receptors in phagocytosis and/or binding of bacteria, which indicates an important role in the cellular immunity and the elimination of apoptotic cells. In this paper, the evolution of the Nimrod superfamily is studied with various methods on the level of genes and repeats. A hypothesis is presented in which the NIM repeat, along with the EMI domain, emerged by structural reorganizations at the end of an EGF-like repeat chain, suggesting a mechanism for the formation of novel types of repeats. The analyses revealed diverse evolutionary patterns in the sequences containing multiple NIM repeats. Although in the Nimrod B and Nimrod C proteins show characteristics of independent evolution, many internal NIM repeats in Eater sequences seem to have undergone concerted evolution. An analysis of the nimrod genes has been performed using phylogenetic and other methods and an evolutionary scenario of the origin and diversification of the Nimrod superfamily is proposed. Our study presents an intriguing example how the evolution of multigene families may contribute to the complexity of the innate immune response
Dynamic Proteomics of Individual Cancer Cells in Response to a Drug
Why do seemingly identical cells respond differently to a drug? To address this, we studied the dynamics and variability of the protein response of human cancer cells to a chemotherapy drug, camptothecin. We present a dynamic-proteomics approach that measures the levels and locations of nearly 1000 different endogenously tagged proteins in individual living cells at high temporal resolution. All cells show rapid translocation of proteins specific to the drug mechanism, including the drug target (topoisomerase-1), and slower, wide-ranging temporal waves of protein degradation and accumulation. However, the cells differ in the behavior of a subset of proteins. We identify proteins whose dynamics differ widely between cells, in a way that corresponds to the outcomes—cell death or survival. This opens the way to understanding molecular responses to drugs in individual cells
The profile of a decaying crystalline cone
The decay of a crystalline cone below the roughening transition is studied.
We consider local mass transport through surface diffusion, focusing on the two
cases of diffusion limited and attachment-detachment limited step kinetics. In
both cases, we describe the decay kinetics in terms of step flow models.
Numerical simulations of the models indicate that in the attachment-detachment
limited case the system undergoes a step bunching instability if the repulsive
interactions between steps are weak. Such an instability does not occur in the
diffusion limited case. In stable cases the height profile, h(r,t), is flat at
radii r<R(t)\sim t^{1/4}. Outside this flat region the height profile obeys the
scaling scenario \partial h/\partial r = {\cal F}(r t^{-1/4}). A scaling ansatz
for the time-dependent profile of the cone yields analytical values for the
scaling exponents and a differential equation for the scaling function. In the
long time limit this equation provides an exact description of the discrete
step dynamics. It admits a family of solutions and the mechanism responsible
for the selection of a unique scaling function is discussed in detail. Finally
we generalize the model and consider permeable steps by allowing direct adatom
hops between neighboring terraces. We argue that step permeability does not
change the scaling behavior of the system, and its only effect is a
renormalization of some of the parameters.Comment: 25 pages, 18 postscript figure
Correlation functions in the two-dimensional random-field Ising model
Transfer-matrix methods are used to study the probability distributions of
spin-spin correlation functions in the two-dimensional random-field Ising
model, on long strips of width sites, for binary field
distributions at generic distance , temperature and field intensity
. For moderately high , and of the order of magnitude used in
most experiments, the distributions are singly-peaked, though rather
asymmetric. For low temperatures the single-peaked shape deteriorates, crossing
over towards a double- ground-state structure. A connection is obtained
between the probability distribution for correlation functions and the
underlying distribution of accumulated field fluctuations. Analytical
expressions are in good agreement with numerical results for ,
low , not too small, and near G=1. From a finite-size {\it ansatz} at
, , averaged correlation functions are predicted to
scale with , . From numerical data we estimate y=0.875 \pm
0.025WR/L=1W \sim h_0^{\kappa} f(L h_0^u)\kappa \simeq 0.45u \simeq 0.8f(x)x \to \inftyW \sim
h_0^{\kappa}d=2$.Comment: RevTeX code for 8 pages, 7 eps figures, to appear in Physical Review
E (1999
Measurement of the Proton and Deuteron Spin Structure Function g_1 in the Resonance Region
We have measured the proton and deuteron spin structure functions g_1^p and
g_1^d in the region of the nucleon resonances for W^2 < 5 GeV^2 and and GeV^2 by inelastically scattering 9.7 GeV polarized
electrons off polarized and targets. We observe
significant structure in g_1^p in the resonance region. We have used the
present results, together with the deep-inelastic data at higher W^2, to
extract . This is the first
information on the low-Q^2 evolution of Gamma toward the Gerasimov-Drell-Hearn
limit at Q^2 = 0.Comment: 7 pages, 2 figure
Search for direct stau production in events with two hadronic tau-leptons in root s=13 TeV pp collisions with the ATLAS detector
A search for the direct production of the supersymmetric partners ofτ-leptons (staus) in final stateswith two hadronically decayingτ-leptons is presented. The analysis uses a dataset of pp collisions corresponding to an integrated luminosity of139fb−1, recorded with the ATLAS detector at the LargeHadron Collider at a center-of-mass energy of 13 TeV. No significant deviation from the expected StandardModel background is observed. Limits are derived in scenarios of direct production of stau pairs with eachstau decaying into the stable lightest neutralino and oneτ-lepton in simplified models where the two staumass eigenstates are degenerate. Stau masses from 120 GeV to 390 GeV are excluded at 95% confidencelevel for a massless lightest neutralino
Single hadron response measurement and calorimeter jet energy scale uncertainty with the ATLAS detector at the LHC
The uncertainty on the calorimeter energy response to jets of particles is
derived for the ATLAS experiment at the Large Hadron Collider (LHC). First, the
calorimeter response to single isolated charged hadrons is measured and
compared to the Monte Carlo simulation using proton-proton collisions at
centre-of-mass energies of sqrt(s) = 900 GeV and 7 TeV collected during 2009
and 2010. Then, using the decay of K_s and Lambda particles, the calorimeter
response to specific types of particles (positively and negatively charged
pions, protons, and anti-protons) is measured and compared to the Monte Carlo
predictions. Finally, the jet energy scale uncertainty is determined by
propagating the response uncertainty for single charged and neutral particles
to jets. The response uncertainty is 2-5% for central isolated hadrons and 1-3%
for the final calorimeter jet energy scale.Comment: 24 pages plus author list (36 pages total), 23 figures, 1 table,
submitted to European Physical Journal
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