1,940 research outputs found
Fluctuation Bounds For Interface Free Energies in Spin Glasses
We consider the free energy difference restricted to a finite volume for
certain pairs of incongruent thermodynamic states (if they exist) in the
Edwards-Anderson Ising spin glass at nonzero temperature. We prove that the
variance of this quantity with respect to the couplings grows proportionally to
the volume in any dimension greater than or equal to two. As an illustration of
potential applications, we use this result to restrict the possible structure
of Gibbs states in two dimensions.Comment: 19 pages, 0 figure
Analysis of transient phosphorylation-dependent protein-protein interactions in living mammalian cells using split-TEV
Abstract Background Regulated protein-protein interactions (PPIs) are pivotal molecular switches that are important for the regulation of signaling processes within eukaryotic cells. Cellular signaling is altered in various disease conditions and offers interesting options for pharmacological interventions. Constitutive PPIs are usually mediated by large interaction domains. In contrast, stimulus-regulated PPIs often depend on small post-translational modifications and are thus better suited targets for drug development. However, the detection of modification-dependent PPIs with biochemical methods still remains a labour- and material-intensive task, and many pivotal PPIs that are potentially suited for pharmacological intervention most likely remain to be identified. The availability of methods to easily identify and quantify stimulus-dependent, potentially also transient interaction events, is therefore essential. The assays should be applicable to intact mammalian cells, optimally also to primary cells in culture. Results In this study, we adapted the split-TEV system to quantify phosphorylation-dependent and transient PPIs that occur at the membrane and in the cytosol of living mammalian cells. Split-TEV is based on a PPI-induced functional complementation of two inactive TEV protease fragments fused to interaction partners of choice. Genetically encoded transcription-coupled and proteolysis-only TEV reporter systems were used to convert the TEV activity into an easily quantifiable readout. We measured the phosphorylation-dependent interaction between the pro-apoptotic protein Bad and the adapter proteins 14-3-3ε and ζ in NIH-3T3 fibroblasts and in primary cultured neurons. Using split-TEV assays, we show that Bad specifically interacts with 14-3-3 isoforms when phosphorylated by protein kinase Akt-1/PKB at Ser136. We also measured the phosphorylation-dependent Bad/14-3-3 interactions mediated by endogenous and transient Akt-1 activity. We furthermore applied split-TEV assays to measure the phosphorylation-dependent interactions of Neuregulin-1-stimulated ErbB4 receptors with several adapter proteins. Conclusion Split-TEV assays are well suited to measure phosphorylation-dependent and transient PPIs that occur specifically at the membrane and in the cytosol of heterologous and primary cultured mammalian cells. Given the high sensitivity of the split-TEV system, all assays were performed in multi-plate formats and could be adapted for higher throughput to screen for pharmacologically active substances.</p
Enhancement of Entanglement Percolation in Quantum Networks via Lattice Transformations
We study strategies for establishing long-distance entanglement in quantum
networks. Specifically, we consider networks consisting of regular lattices of
nodes, in which the nearest neighbors share a pure, but non-maximally entangled
pair of qubits. We look for strategies that use local operations and classical
communication. We compare the classical entanglement percolation protocol, in
which every network connection is converted with a certain probability to a
singlet, with protocols in which classical entanglement percolation is preceded
by measurements designed to transform the lattice structure in a way that
enhances entanglement percolation. We analyze five examples of such comparisons
between protocols and point out certain rules and regularities in their
performance as a function of degree of entanglement and choice of operations.Comment: 12 pages, 17 figures, revtex4. changes from v3: minor stylistic
changes for journal reviewer, minor changes to figures for journal edito
Linearity of cortical receptive fields measured with natural sounds
How do cortical neurons represent the acoustic environment? This question is often addressed by probing with simple stimuli such as clicks or tone pips. Such stimuli have the advantage of yielding easily interpreted answers, but have the disadvantage that they may fail to uncover complex or higher-order neuronal response properties. Here, we adopt an alternative approach, probing neuronal responses with complex acoustic stimuli, including animal vocalizations. We used in vivo whole-cell methods in the rat auditory cortex to record subthreshold membrane potential fluctuations elicited by these stimuli. Most neurons responded robustly and reliably to the complex stimuli in our ensemble. Using regularization techniques, we estimated the linear component, the spectrotemporal receptive field (STRF), of the transformation from the sound (as represented by its time-varying spectrogram) to the membrane potential of the neuron. We find that the STRF has a rich dynamical structure, including excitatory regions positioned in general accord with the prediction of the classical tuning curve. However, whereas the STRF successfully predicts the responses to some of the natural stimuli, it surprisingly fails completely to predict the responses to others; on average, only 11% of the response power could be predicted by the STRF. Therefore, most of the response of the neuron cannot be predicted by the linear component, although the response is deterministically related to the stimulus. Analysis of the systematic errors of the STRF model shows that this failure cannot be attributed to simple nonlinearities such as adaptation to mean intensity, rectification, or saturation. Rather, the highly nonlinear response properties of auditory cortical neurons must be attributable to nonlinear interactions between sound frequencies and time-varying properties of the neural encoder
Disorder-Induced Order in Quantum XY Chains
We observe signatures of disorder-induced order in 1D XY spin chains with an
external, site-dependent uni-axial random field within the XY plane. We
numerically investigate signatures of a quantum phase transition at T=0, in
particular an upsurge of the magnetization in the direction orthogonal to the
external magnetic field, and the scaling of the block-entropy with the
amplitude of this field. Also, we discuss possible realizations of this effect
in ultra-cold atom experiments
Primary gas thermometry by means of laser-absorption spectroscopy: Determination of the Boltzmann constant
We report on a new optical implementation of primary gas thermometry based on
laser absorption spectrometry in the near infrared. The method consists in
retrieving the Doppler broadening from highly accurate observations of the line
shape of the R(12) transition in
CO gas at thermodynamic equilibrium. Doppler width measurements as a
function of gas temperature, ranging between the triple point of water and the
gallium melting point, allowed for a spectroscopic determination of the
Boltzmann constant with a relative accuracy of .Comment: Submitted to Physical Review Letter
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