141 research outputs found
Measurement of the electric dipole moments for transitions to rubidium Rydberg states via Autler-Townes splitting
We present the direct measurements of electric-dipole moments for
transitions with for Rubidium atoms. The
measurements were performed in an ultracold sample via observation of the
Autler-Townes splitting in a three-level ladder scheme, commonly used for
2-photon excitation of Rydberg states. To the best of our knowledge, this is
the first systematic measurement of the electric dipole moments for transitions
from low excited states of rubidium to Rydberg states. Due to its simplicity
and versatility, this method can be easily extended to other transitions and
other atomic species with little constraints. Good agreement of the
experimental results with theory proves the reliability of the measurement
method.Comment: 12 pages, 6 figures; figure 6 replaced with correct versio
Electronic temperatures, densities and plasma X-ray emission of a 14.5 GHz Electron-Cyclotron Resonance Ion Source
We have performed a systematic study of the Bremsstrahlung emission from the
electrons in the plasma of a commercial 14.5 GHz Electron-Cyclotron Resonance
Ion Source. The electronic spectral temperature and the product of ionic and
electronic densities of the plasma are measured by analyzing the Bremsstrahlung
spectra recorded for several rare gases (Ar, Kr, Xe) as a function of the
injected power. Within our uncertainty, we find an average temperature of ? 48
keV above 100W, with a weak dependency on the injected power and gas
composition. Charge state distributions of extracted ion beams have been
determined as well, providing a way to disentangle the ionic density from the
electronic density. Moreover X-ray emission from highly charged argon ions in
the plasma has been observed with a high-resolution mosaic crystal
spectrometer, demonstrating the feasibility for high-precision measurements of
transition energies of highly charged ions, in particular of the magnetic
dipole (M1) transition of He-like of argon ions
Observation of coherent many-body Rabi oscillations
A two-level quantum system coherently driven by a resonant electromagnetic
field oscillates sinusoidally between the two levels at frequency
which is proportional to the field amplitude [1]. This phenomenon, known as the
Rabi oscillation, has been at the heart of atomic, molecular and optical
physics since the seminal work of its namesake and coauthors [2]. Notably, Rabi
oscillations in isolated single atoms or dilute gases form the basis for
metrological applications such as atomic clocks and precision measurements of
physical constants [3]. Both inhomogeneous distribution of coupling strength to
the field and interactions between individual atoms reduce the visibility of
the oscillation and may even suppress it completely. A remarkable
transformation takes place in the limit where only a single excitation can be
present in the sample due to either initial conditions or atomic interactions:
there arises a collective, many-body Rabi oscillation at a frequency
involving all N >> 1 atoms in the sample [4]. This is true even
for inhomogeneous atom-field coupling distributions, where single-atom Rabi
oscillations may be invisible. When one of the two levels is a strongly
interacting Rydberg level, many-body Rabi oscillations emerge as a consequence
of the Rydberg excitation blockade. Lukin and coauthors outlined an approach to
quantum information processing based on this effect [5]. Here we report initial
observations of coherent many-body Rabi oscillations between the ground level
and a Rydberg level using several hundred cold rubidium atoms. The strongly
pronounced oscillations indicate a nearly complete excitation blockade of the
entire mesoscopic ensemble by a single excited atom. The results pave the way
towards quantum computation and simulation using ensembles of atoms
Observation of mesoscopic crystalline structures in a two-dimensional Rydberg gas
The ability to control and tune interactions in ultracold atomic gases has
paved the way towards the realization of new phases of matter. Whereas
experiments have so far achieved a high degree of control over short-ranged
interactions, the realization of long-range interactions would open up a whole
new realm of many-body physics and has become a central focus of research.
Rydberg atoms are very well-suited to achieve this goal, as the van der Waals
forces between them are many orders of magnitude larger than for ground state
atoms. Consequently, the mere laser excitation of ultracold gases can cause
strongly correlated many-body states to emerge directly when atoms are
transferred to Rydberg states. A key example are quantum crystals, composed of
coherent superpositions of different spatially ordered configurations of
collective excitations. Here we report on the direct measurement of strong
correlations in a laser excited two-dimensional atomic Mott insulator using
high-resolution, in-situ Rydberg atom imaging. The observations reveal the
emergence of spatially ordered excitation patterns in the high-density
components of the prepared many-body state. They have random orientation, but
well defined geometry, forming mesoscopic crystals of collective excitations
delocalised throughout the gas. Our experiment demonstrates the potential of
Rydberg gases to realise exotic phases of matter, thereby laying the basis for
quantum simulations of long-range interacting quantum magnets.Comment: 10 pages, 7 figure
The Prion Protein Ligand, Stress-Inducible Phosphoprotein 1, Regulates Amyloid-beta Oligomer Toxicity
In Alzheimer\u27s disease (AD), soluble amyloid-beta oligomers (A beta Os) trigger neurotoxic signaling, at least partially, via the cellular prion protein (PrPC). However, it is unknown whether other ligands of PrPC can regulate this potentially toxic interaction. Stress-inducible phosphoprotein 1 (STI1), an Hsp90 cochaperone secreted by astrocytes, binds to PrPC in the vicinity of the A beta O binding site to protect neurons against toxic stimuli. Here, we investigated a potential role of STI1 in A beta O toxicity. We confirmed the specific binding of A beta Os and STI1 to the PrP and showed that STI1 efficiently inhibited A beta O binding to PrP in vitro (IC50 of similar to 70 nM) and also decreased A beta O binding to cultured mouse primary hippocampal neurons. Treatment with STI1 prevented A beta O-induced synaptic loss and neuronal death in mouse cultured neurons and long-term potentiation inhibition in mouse hippocampal slices. Interestingly, STI1-haploinsufficient neurons were more sensitive to A beta O-induced cell death and could be rescued by treatment with recombinant STI1. Noteworthy, both A beta O binding to PrPC and PrPC-dependent A beta O toxicity were inhibited by TPR2A, the PrPC-interacting domain of STI1. Additionally, PrPC-STI1 engagement activated alpha 7 nicotinic acetylcholine receptors, which participated in neuroprotection against A beta O-induced toxicity. We found an age-dependent upregulation of cortical STI1 in the APPswe/PS1dE9 mouse model of AD and in the brains of AD-affected individuals, suggesting a compensatory response. Our findings reveal a previously unrecognized role of the PrPC ligand STI1 in protecting neurons in AD and suggest a novel pathway that may help to offset A beta O-induced toxicity
TraR, a Homolog of a RNAP Secondary Channel Interactor, Modulates Transcription
Recent structural and biochemical studies have identified a novel control mechanism of gene expression mediated through the secondary channel of RNA Polymerase (RNAP) during transcription initiation. Specifically, the small nucleotide ppGpp, along with DksA, a RNAP secondary channel interacting factor, modifies the kinetics of transcription initiation, resulting in, among other events, down-regulation of ribosomal RNA synthesis and up-regulation of several amino acid biosynthetic and transport genes during nutritional stress. Until now, this mode of regulation of RNAP was primarily associated with ppGpp. Here, we identify TraR, a DksA homolog that mimics ppGpp/DksA effects on RNAP. First, expression of TraR compensates for dksA transcriptional repression and activation activities in vivo. Second, mutagenesis of a conserved amino acid of TraR known to be critical for DksA function abolishes its activity, implying both structural and functional similarity to DksA. Third, unlike DksA, TraR does not require ppGpp for repression of the rrnB P1 promoter in vivo and in vitro or activation of amino acid biosynthesis/transport genes in vivo. Implications for DksA/ppGpp mechanism and roles of TraR in horizontal gene transfer and virulence are discussed
The F0F1-ATP Synthase Complex Contains Novel Subunits and Is Essential for Procyclic Trypanosoma brucei
The mitochondrial F0F1 ATP synthase is an essential multi-subunit protein complex in the vast majority of eukaryotes but little is known about its composition and role in Trypanosoma brucei, an early diverged eukaryotic pathogen. We purified the F0F1 ATP synthase by a combination of affinity purification, immunoprecipitation and blue-native gel electrophoresis and characterized its composition and function. We identified 22 proteins of which five are related to F1 subunits, three to F0 subunits, and 14 which have no obvious homology to proteins outside the kinetoplastids. RNAi silencing of expression of the F1 α subunit or either of the two novel proteins showed that they are each essential for the viability of procyclic (insect stage) cells and are important for the structural integrity of the F0F1-ATP synthase complex. We also observed a dramatic decrease in ATP production by oxidative phosphorylation after silencing expression of each of these proteins while substrate phosphorylation was not severely affected. Our procyclic T. brucei cells were sensitive to the ATP synthase inhibitor oligomycin even in the presence of glucose contrary to earlier reports. Hence, the two novel proteins appear essential for the structural organization of the functional complex and regulation of mitochondrial energy generation in these organisms is more complicated than previously thought
Histone Deacetylase 3 Depletion in Osteo/Chondroprogenitor Cells Decreases Bone Density and Increases Marrow Fat
Histone deacetylase (Hdac)3 is a nuclear enzyme that contributes to epigenetic programming and is required for embryonic development. To determine the role of Hdac3 in bone formation, we crossed mice harboring loxP sites around exon 7 of Hdac3 with mice expressing Cre recombinase under the control of the osterix promoter. The resulting Hdac3 conditional knockout (CKO) mice were runted and had severe deficits in intramembranous and endochondral bone formation. Calvarial bones were significantly thinner and trabecular bone volume in the distal femur was decreased 75% in the Hdac3 CKO mice due to a substantial reduction in trabecular number. Hdac3-CKO mice had fewer osteoblasts and more bone marrow adipocytes as a proportion of tissue area than their wildtype or heterozygous littermates. Bone formation rates were depressed in both the cortical and trabecular regions of Hdac3 CKO femurs. Microarray analyses revealed that numerous developmental signaling pathways were affected by Hdac3-deficiency. Thus, Hdac3 depletion in osterix-expressing progenitor cells interferes with bone formation and promotes bone marrow adipocyte differentiation. These results demonstrate that Hdac3 inhibition is detrimental to skeletal health
Systems of Differential Algebraic Equations in Computational Electromagnetics
Starting from space-discretisation of Maxwell's equations, various classical
formulations are proposed for the simulation of electromagnetic fields. They
differ in the phenomena considered as well as in the variables chosen for
discretisation. This contribution presents a literature survey of the most
common approximations and formulations with a focus on their structural
properties. The differential-algebraic character is discussed and quantified by
the differential index concept
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