10,341 research outputs found

    Do mixtures of bosonic and fermionic atoms adiabatically heat up in optical lattices?

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    Mixtures of bosonic and fermionic atoms in optical lattices provide a promising arena to study strongly correlated systems. In experiments realizing such mixtures in the quantum degenerate regime the temperature is a key parameter. In this work, we investigate the intrinsic heating and cooling effects due to an entropy-preserving raising of the optical lattice potential. We analyze this process, identify the generic behavior valid for a wide range of parameters, and discuss it quantitatively for the recent experiments with 87Rb and 40K atoms. In the absence of a lattice, we treat the bosons in the Hartree-Fock-Bogoliubov-Popov-approximation, including the fermions in a self-consistent mean field interaction. In the presence of the full three-dimensional lattice, we use a strong coupling expansion. As a result of the presence of the fermions, the temperature of the mixture after the lattice ramp-up is always higher than for the pure bosonic case. This sheds light onto a key point in the analysis of recent experiments.Comment: 5 pages, 3 figure

    Structural basis of transcription initiation by RNA polymerase II.

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    Transcription of eukaryotic protein-coding genes commences with the assembly of a conserved initiation complex, which consists of RNA polymerase II (Pol II) and the general transcription factors, at promoter DNA. After two decades of research, the structural basis of transcription initiation is emerging. Crystal structures of many components of the initiation complex have been resolved, and structural information on Pol II complexes with general transcription factors has recently been obtained. Although mechanistic details await elucidation, available data outline how Pol II cooperates with the general transcription factors to bind to and open promoter DNA, and how Pol II directs RNA synthesis and escapes from the promoter

    New CP-violation and preferred-frame tests with polarized electrons

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    We used a torsion pendulum containing 9×1022\sim 9 \times 10^{22} polarized electrons to search for CP-violating interactions between the pendulum's electrons and unpolarized matter in the laboratory's surroundings or the sun, and to test for preferred-frame effects that would precess the electrons about a direction fixed in inertial space. We find gPegSN/(c)<1.7×1036|g_{\rm P}^e g_{\rm S}^N|/(\hbar c)< 1.7 \times 10^{-36} and gAegVN/(c)<4.8×1056|g_{\rm A}^e g_{\rm V}^N|/(\hbar c) < 4.8 \times 10^{-56} for λ>1\lambda > 1AU. Our preferred-frame constraints, interpreted in the Kosteleck\'y framework, set an upper limit on the parameter b~e5.0×1021|\bm{\tilde {b}}^e| \leq 5.0 \times 10^{-21} eV that should be compared to the benchmark value me2/MPlanck=2×1017m_e^2/M_{\rm Planck}= 2 \times 10^{-17} eV.Comment: 4 figures, accepted for publication in Physical Review Letter

    Structure of an inactive RNA polymerase II dimer

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    Eukaryotic gene transcription is carried out by three RNA polymerases: Pol I, Pol II and Pol III. Although it has long been known that Pol I can form homodimers, it is unclear whether and how the two other RNA polymerases dimerize. Here we present the cryo-electron microscopy (cryo-EM) structure of a mammalian Pol II dimer at 3.5 Å resolution. The structure differs from the Pol I dimer and reveals that one Pol II copy uses its RPB4-RPB7 stalk to penetrate the active centre cleft of the other copy, and vice versa, giving rise to a molecular handshake. The polymerase clamp domain is displaced and mobile, and the RPB7 oligonucleotide-binding fold mimics the DNA–RNA hybrid that occupies the cleft during active transcription. The Pol II dimer is incompatible with nucleic acid binding as required for transcription and may represent an inactive storage form of the polymerase

    Parametric instabilities in magnetized multicomponent plasmas

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    This paper investigates the excitation of various natural modes in a magnetized bi-ion or dusty plasma. The excitation is provided by parametrically pumping the magnetic field. Here two ion-like species are allowed to be fully mobile. This generalizes our previous work where the second heavy species was taken to be stationary. Their collection of charge from the background neutral plasma modifies the dispersion properties of the pump and excited waves. The introduction of an extra mobile species adds extra modes to both these types of waves. We firstly investigate the pump wave in detail, in the case where the background magnetic field is perpendicular to the direction of propagation of the pump wave. Then we derive the dispersion equation relating the pump to the excited wave for modes propagating parallel to the background magnetic field. It is found that there are a total of twelve resonant interactions allowed, whose various growth rates are calculated and discussed.Comment: Published in May 2004; this is a late submission to the archive. 14 pages, 8 figure

    Chosen-ciphertext security from subset sum

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    We construct a public-key encryption (PKE) scheme whose security is polynomial-time equivalent to the hardness of the Subset Sum problem. Our scheme achieves the standard notion of indistinguishability against chosen-ciphertext attacks (IND-CCA) and can be used to encrypt messages of arbitrary polynomial length, improving upon a previous construction by Lyubashevsky, Palacio, and Segev (TCC 2010) which achieved only the weaker notion of semantic security (IND-CPA) and whose concrete security decreases with the length of the message being encrypted. At the core of our construction is a trapdoor technique which originates in the work of Micciancio and Peikert (Eurocrypt 2012

    Learning to perform a new movement with robotic assistance: comparison of haptic guidance and visual demonstration

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    BACKGROUND: Mechanical guidance with a robotic device is a candidate technique for teaching people desired movement patterns during motor rehabilitation, surgery, and sports training, but it is unclear how effective this approach is as compared to visual demonstration alone. Further, little is known about motor learning and retention involved with either robot-mediated mechanical guidance or visual demonstration alone. METHODS: Healthy subjects (n = 20) attempted to reproduce a novel three-dimensional path after practicing it with mechanical guidance from a robot. Subjects viewed their arm as the robot guided it, so this "haptic guidance" training condition provided both somatosensory and visual input. Learning was compared to reproducing the movement following only visual observation of the robot moving along the path, with the hand in the lap (the "visual demonstration" training condition). Retention was assessed periodically by instructing the subjects to reproduce the path without robotic demonstration. RESULTS: Subjects improved in ability to reproduce the path following practice in the haptic guidance or visual demonstration training conditions, as evidenced by a 30–40% decrease in spatial error across 126 movement attempts in each condition. Performance gains were not significantly different between the two techniques, but there was a nearly significant trend for the visual demonstration condition to be better than the haptic guidance condition (p = 0.09). The 95% confidence interval of the mean difference between the techniques was at most 25% of the absolute error in the last cycle. When asked to reproduce the path repeatedly following either training condition, the subjects' performance degraded significantly over the course of a few trials. The tracing errors were not random, but instead were consistent with a systematic evolution toward another path, as if being drawn to an "attractor path". CONCLUSION: These results indicate that both forms of robotic demonstration can improve short-term performance of a novel desired path. The availability of both haptic and visual input during the haptic guidance condition did not significantly improve performance compared to visual input alone in the visual demonstration condition. Further, the motor system is inclined to repeat its previous mistakes following just a few movements without robotic demonstration, but these systematic errors can be reduced with periodic training

    The thermal and two-particle stress-energy must be ill-defined on the 2-d Misner space chronology horizon

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    We show that an analogue of the (four dimensional) image sum method can be used to reproduce the results, due to Krasnikov, that for the model of a real massless scalar field on the initial globally hyperbolic region IGH of two-dimensional Misner space there exist two-particle and thermal Hadamard states (built on the conformal vacuum) such that the (expectation value of the renormalised) stress-energy tensor in these states vanishes on IGH. However, we shall prove that the conclusions of a general theorem by Kay, Radzikowski and Wald still apply for these states. That is, in any of these states, for any point b on the Cauchy horizon and any neighbourhood N of b, there exists at least one pair of non-null related points (x,x'), with x and x' in the intersection of IGH with N, such that (a suitably differentiated form of) its two-point function is singular. (We prove this by showing that the two-point functions of these states share the same singularities as the conformal vacuum on which they are built.) In other words, the stress-energy tensor in any of these states is necessarily ill-defined on the Cauchy horizon.Comment: 6 pages, LaTeX, RevTeX, no figure

    Structure of the human Mediator-RNA polymerase II pre-initiation complex

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    Mediator is a conserved coactivator that enables regulated transcription initiation at eukaryotic genes1–3. Mediator is recruited by transcriptional activators and binds the pre-initiation complex (PIC) to stimulate RNA polymerase II (Pol II) phosphorylation and promoter escape1–6. Here we prepare a recombinant human Mediator, reconstitute a 50-subunit Mediator-PIC complex, and determine the structure of the complex by cryo-EM. Mediator uses its head module to contact the Pol II stalk and the general transcription factors TFIIB and TFIIE, resembling the Mediator-PIC interactions in the corresponding yeast complex7–9. The metazoan subunits MED27-MED30 associate with exposed regions in MED14 and MED17 to form the proximal part of the Mediator tail module that binds activators. Mediator positions the flexibly linked CDK-activating kinase (CAK) of the general transcription factor TFIIH near the linker to the C-terminal repeat domain (CTD) of Pol II. The Mediator shoulder domain holds the CAK subunit CDK7, whereas the hook domain contacts a CDK7 element that flanks the kinase active site. The shoulder and hook reside in the Mediator head and middle modules, respectively, which can move relative to each other and may induce an active conformation of the CDK7 kinase to allosterically stimulate CTD phosphorylation
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