Hasil untuk "physics.atom-ph"

Roy Eid, Alfred Hammond, Lucas Lavoine et al.

We realize textbook experiments on Bose-Einstein condensate tunnelling through thin repulsive potential barriers. In particular, we demonstrate atom tunnelling though a single optical barrier in the quantum scattering regime where the De Broglie wavelength of the atoms is larger than the barrier width. Such a beam splitter can be used for atom interferometry and we study the case of two barriers creating an atomic Fabry-P{é}rot cavity. Technically, the velocity of the atoms is reduced thanks to the use of a 39K Bose-Einstein condensate with no interactions. The potential barriers are created optically and their width is tunable thanks to the use of a digital micro-mirror device. In addition, our scattering experiments enable in-situ characterization of the optical aberrations of the barrier optical system.

J. Lawson, R. Veech

The observed equilibrium constants (Kobs) of the creatine kinase (EC 2.7.3.2), myokinase (EC 2.7.4.3), glucose-6-phosphatase (EC 3.1.3.9), and fructose-1,6-diphosphatase (EC 3.1.3.11) reactions have been determined at 38 degrees C, pH 7.0, ionic strength 0.25, and varying free magnesium concentrations. The equilibrium constant (KCK) for the creatine kinase reaction defined as: KCK = [sigma ATP] [sigma creatine] divided by ([sigma ADP] [sigma creatine-P] [H+]) was measured at 0.25 ionic strength and 38 degrees C and was shown to vary with free [Mg2+]. The value was found to be 3.78 x 10(8) M-1 at free [Mg2+] = 0 and 1.66 x 10(9) M-1 at free [Mg2+] = 10(-3) M. Therefore, at pH 7.0, the value of Kobs, defined as Kobs = KCK[H+] = [sigma ATP] [sigma creatine] divided by ([sigma ADP] [sigma creatine-P] was 37.8 at free [Mg2+] = 0 and 166 at free [Mg2+] = 10(-3) M. The Kobs value for the myokinase reaction, 2 sigma ADP equilibrium sigma AMP + sigma ATP, was found to vary with free [Mg2+], being 0.391 at free [Mg2+] = 0 and 1.05 at free [Mg2+] = 10(-3) M. Taking the standard state of water to have activity equal to 1, the Kobs of glucose-6-P hydrolysis, sigma glucose-6-P + H2O equilibrium sigma glucose + sigma Pi, was found not to vary with free [Mg2+], being 110 M at both free [Mg2+] = 0 and free [Mg2+] = 10(-3) M. The Kobs of fructose-1,6-P2 hydrolysis, sigma fructose-1,6-P2 equilibrium sigma fructose-6-P + sigma Pi, was found to vary with free [Mg2+], being 272 M at free [Mg2+] = 0 and 174 M at free [Mg2+] = 0.89 x 10(-3) M.

L. Tronstad, J. Andreasen, G. Hasselgren et al.

F. Maxfield

It has been shown that endocytic vesicles in BALB/c 3T3 cells have a pH of 5.0 (Tycko and Maxfield, Cell, 28:643-651). In this paper, a method for measuring the effect of various agents, including weak bases and ionophores, on the pH of endocytic vesicles is presented. The method is based on the increase in fluorescein fluorescence with 490-nm excitation as the pH is raised above 5.0. Intensities of cells were measured using a microscope spectrofluorometer after internalization of fluorescein-labeled alpha 2-macroglobulin by receptor-mediated endocytosis. The increase in endocytic vesicle pH was determined from the increase in fluorescence after addition of various concentrations of the test agents. The following agents increased endocytic vesicle pH above 6.0 at the indicated concentrations: monensin (6 microM), FCCP (10 microM), chloroquine (140 microM), ammonia (5 mM), methylamine (10 mM). The ability of many of these agents to raise endocytic vesicle pH may account for many of their effects on receptor-mediated endocytosis. Dansylcadaverine caused no effect on vesicle pH at 1 mM. The observed increases in vesicle pH were rapid (1-2 min) and could be reversed by removal of the perturbant. This reversibility indicates that the vesicles themselves contain a mechanism for acidification. The increase in vesicle pH due to these treatments can be observed visually using an SIT video camera. Using this method, it is shown that endocytic vesicles become acidic at very early times (i.e., within 5-7 min of continuous uptake at 37 degrees C).

G. Wiener, J. Richter, J. Copper et al.

D. Comparat

We discuss the possibility to enhance the sensitivity of optical interferometric devices by increasing its open area using an external field gradient that act differently on the two arms of the interfer-ometers. The use of combined electric and magnetic field cancel non linear terms that dephases the interferometer. This is possible using well defined (typically with n $\sim$ 20 Rydberg) states, a magnetic field of few Tesla and an electric field gradient of $\sim$ 10V/cm 2. However this allows only for interaction times on the order of tens of $μ$s leading a reachable accuracy of only 1 or 2 order of magnitude higher than standard light-pulse atom interferometers. Furthermore, the control of fields and states and 3D trajectories puts severe limits to the reachable accuracy. This idea is therefore not suitable for precision measurement but might eventually be used for gravity or neutrality in antimatter studies.

Rosario Gonzalez-Ferez, Janine Shertzer, H. R. Sadeghpour

We predict that ultralong-range Rydberg bi-molecules form in collisions between polar molecules in cold and ultracold settings. The collision of $Λ$-doublet nitric oxide (NO) with long-lived Rydberg NO($nf$, $ng$) molecules forms ultralong-range Rydberg bi-molecules with GHz energies and kilo-Debye permanent electric dipole moments. The Hamiltonian includes both the anisotropic charge-molecular dipole interaction and the electron-NO scattering. The rotational constant for the Rydberg bi-molecules is in the MHz range, allowing for microwave spectroscopy of rotational transitions in Rydberg bi-molecules. Considerable orientation of NO dipole can be achieved. The Rydberg molecules described here hold promise for studies of a special class of long-range bi-molecular interactions.

L. Brannon-Peppas, N. Peppas

Z. Wang, R. Delaune, W. H. Patrick et al.

Feng Xu

The electronic absorption spectrum, susceptibility to fluoride inhibition, redox potential, and substrate turnover of several fungal laccases have been explored as a function of pH. The laccases showed a single spectrally detectable acid-base transition at pH 6-9 and a fluoride inhibition that diminished by increased pH (indicating a competition with hydroxide inhibition). Relatively small changes in the redox potentials (≤0.1 V) of laccase were observed over the pH 2.7-11. Under the catalysis of laccase, the apparent oxidation rates (kcat and kcat/Km) of two nonphenolic substrates, potassium ferrocyanide and 2,2′-azinobis-(3-ethylbenzthiazoline-6-sulfonic acid),decreased monotonically as the pH increased. In contrast, the apparent oxidation rates (kcat and kcat/Km) of three 2,6-dimethoxyphenols (whose pKa values range from 7.0 to 8.7) exhibited bell-shaped pH profiles whose maxima were distinct for each laccase but independent of the substrate. By correlating these pH dependences, it is proposed that the balance of two opposing effects, one generated by the redox potential difference between a reducing substrate and the type 1 copper of laccase (which correlates to the electron transfer rate and is favored for a phenolic substrate by higher pH) and another generated by the binding of a hydroxide anion to the type 2/type 3 coppers of laccase (which inhibits the activity at higher pH), contributes to the pH activity profile of the fungal laccases.

I. J. Buerge, S. Hug

Wesley C. Campbell, Eric R. Hudson

The interaction between the electric dipole moment of a trapped molecular ion and the configuration of the confined Coulomb crystal couples the orientation of the molecule to its motion. We consider the practical feasibility of harnessing this interaction to initialize, process, and read out quantum information encoded in molecular ion qubits without optically illuminating the molecules. We present two schemes wherein a molecular ion can be entangled with a co-trapped atomic ion qubit, providing, among other things, a means for molecular state preparation and measurement. We also show that virtual phonon exchange can significantly boost range of the intermolecular dipole-dipole interaction, allowing strong coupling between widely-separated molecular ion qubits.

M. Dockal, D. Carter, F. Rüker

Human serum albumin (HSA) is a protein of 66.5 kDa that is composed of three homologous domains, each of which displays specific structural and functional characteristics. HSA is known to undergo different pH-dependent structural transitions, the N-F and F-E transitions in the acid pH region and the N-B transition at slightly alkaline pH. In order to elucidate the structural behavior of the recombinant HSA domains as stand-alone proteins and to investigate the molecular and structural origins of the pH-induced conformational changes of the intact molecule, we have employed fluorescence and circular dichroic methods. Here we provide evidence that the loosening of the HSA structure in the N-F transition takes place primarily in HSA-DOM III and that HSA-DOM I undergoes a structural rearrangement with only minor changes in secondary structure, whereas HSA-DOM II transforms to a molten globule-like state as the pH is reduced. In the pH region of the N-B transition of HSA, HSA-DOM I and HSA-DOM II experience a tertiary structural isomerization, whereas with HSA-DOM III no alterations in tertiary structure are observed, as judged from near-UV CD and fluorescence measurements.

Krystian Sycz, Adam M. Wojciechowski, Wojciech Gawlik

We report on the creation, observation and optimization of superposition states of cold atoms. In our experiments, rubidium atoms are prepared in a magneto-optical trap and later, after switching off the trapping fields, Faraday rotation of a weak probe beam is used to characterize atomic states prepared by application of appropriate light pulses and external magnetic fields. We discuss the signatures of polarization and alignment of atomic spin states and identify main factors responsible for deterioration of the atomic number and their coherence and present means for their optimization, like relaxation in the dark with the strobe probing. These results may be used for controlled preparation of cold atom samples and in situ magnetometry of static and transient fields

Nitzan Akerman, Roee Ozeri

Atomic clocks use atomic transitions as frequency references. The susceptibility of the atomic transition to external fields limits clock stability and introduces systematic frequency shifts. Here, we propose to realize an atomic clock that utilizes an entangled superposition of states of multiple atomic species, where the reference frequency is a sum of the individual transition frequencies. The superposition is selected such that the susceptibilities of the respective transitions, in individual species, destructively interfere leading to improved stability and reduced systematic shifts. We present and analyze two examples of such combinations. The first uses the optical quadrupole transitions in a $^{40}$Ca$^+$ - $^{174}$Yb$^+$ two-ion crystal. The second is a superposition of optical quadrupole transitions in one $^{88}$Sr$^+$ ion and three $^{202}$Hg$^+$ ions. These combinations have reduced susceptibility to external magnetic fields and blackbody radiation.

M. A. Almajid, M. Zabel, S. Skruszewicz et al.

Momentum-resolved photoelectron emission from xenon in colinearly polarized two-color laser fields at above-threshold ionization conditions is studied both experimentally and theoretically. We utilize phase-of-the-phase spectroscopy as recently introduced by Skruszewicz et al., Phys. Rev. Lett. 115, 043001 (2015) to analyze the dependence of the yields on the relative phase $\varphi$ between the fundamental and second harmonic laser fields. The resulting phase-of-phase spectra feature a characteristic checkerboard pattern, which can analytically be described within the strong-field approximation.

K. Loftin, C. Adams, M. Meyer et al.

P. Maiti, T. Çagin, Shiang‐Tai Lin et al.

P. J. Hansen

C. Hsiao, C. Chiou, J. Yang