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1.
Nature ; 455(7217): 1216-9, 2008 Oct 30.
Article in English | MEDLINE | ID: mdl-18830245

ABSTRACT

Entanglement, a key feature of quantum mechanics, is a resource that allows the improvement of precision measurements beyond the conventional bound attainable by classical means. This results in the standard quantum limit, which is reached in today's best available sensors of various quantities such as time and position. Many of these sensors are interferometers in which the standard quantum limit can be overcome by using quantum-entangled states (in particular spin squeezed states) at the two input ports. Bose-Einstein condensates of ultracold atoms are considered good candidates to provide such states involving a large number of particles. Here we demonstrate spin squeezed states suitable for atomic interferometry by splitting a condensate into a few parts using a lattice potential. Site-resolved detection of the atoms allows the measurement of the atom number difference and relative phase, which are conjugate variables. The observed fluctuations imply entanglement between the particles, a resource that would allow a precision gain of 3.8 dB over the standard quantum limit for interferometric measurements.

2.
Phys Rev Lett ; 95(15): 150406, 2005 Oct 07.
Article in English | MEDLINE | ID: mdl-16241705

ABSTRACT

We have investigated the expansion of a Bose-Einstein condensate of strongly magnetic chromium atoms. The long-range and anisotropic magnetic dipole-dipole interaction leads to an anisotropic deformation of the expanding chromium condensate which depends on the orientation of the atomic dipole moments. Our measurements are consistent with the theory of dipolar quantum gases and show that a chromium condensate is an excellent model system to study dipolar interactions in such gases.

3.
Phys Rev Lett ; 94(6): 061302, 2005 Feb 18.
Article in English | MEDLINE | ID: mdl-15783717

ABSTRACT

I present a microscopic description of Hawking radiation in sonic black holes. A one-dimensional Fermi-degenerate liquid squeezed by a smooth barrier forms a transonic flow, a sonic analog of a black hole. The quantum treatment of the noninteracting case establishes a close relationship between sonic Hawking radiation and quantum tunneling through the barrier. Quasiparticle excitations appear at the barrier and are then radiated with a thermal distribution in exact agreement with Hawking's formula. The signature of the radiation can be found in the dynamic structure factor, which can be measured in a scattering experiment. The possibility for experimental verification of this new transport phenomenon for ultracold atoms is discussed.

4.
Phys Rev Lett ; 90(11): 110402, 2003 Mar 21.
Article in English | MEDLINE | ID: mdl-12688918

ABSTRACT

A gaseous Bose-Einstein condensate irradiated by a far off-resonance laser has long-range interatomic correlations caused by laser-induced dipole-dipole interactions. These correlations, which are tunable via the laser intensity and frequency, can produce a "roton" minimum in the excitation spectrum--behavior reminiscent of the strongly correlated superfluid liquid He II.

5.
Phys Rev Lett ; 88(13): 130402, 2002 Apr 01.
Article in English | MEDLINE | ID: mdl-11955085

ABSTRACT

We show that the dipole-dipole interatomic forces induced by an off-resonant running laser beam can lead to a self-bound pencil-shaped Bose condensate, even if the laser beam is a plane wave. For an appropriate laser intensity the ground state has a quasi-one-dimensional density modulation-a Bose-Einstein "supersolid."

6.
Cancer Epidemiol Biomarkers Prev ; 10(1): 59-64, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11205490

ABSTRACT

Repeated measurement of ovarian steroids in saliva could provide an advantage in studies estimating long-term sex steroid exposure in premenopausal women, by reducing the measurement error associated with collection of serum or urine samples. We previously reported on characteristics of ultrasensitive RIAs adapted for extraction-free measurement of estradiol (E2) and progesterone (PG) in saliva. The purpose of the present study was to evaluate the consistency of E2 and PG levels in saliva in the same women across menstrual cycles, and to compare this with the variation observed between women. We also evaluated the effect of altering the number of consecutive daily samples considered and the method for locating a particular cycle day in relation to ovulation (day 0). Study participants included 12 healthy women who provided daily saliva samples for two consecutive, ovulatory menstrual cycles. A single midluteal serum sample was collected 7-8 days after detection of a luteinizing hormone (LH) peak in urine. We plotted individual cycle profiles and computed intraclass correlation coefficients (ICC) for various definitions of peak and cumulative daily hormone level. For peak PG, determined as the maximal running 3-day mean, ICC was 0.68. For cumulative PG, based on 8 consecutive cycle days (+2 to +9), ICCs were 0.72-0.76 when reverse dating LH peak or rise in salivary PG determined day 0. For E2, ICCs ranged from 0.74 to 0.79 by various dating methods for the 5 preovulatory days (-4-0), and from 0.85 to 0.92 for the 15 days about the center of the cycle (-6 to +8). With exclusion of just the first 5 days of the cycle, the ICC for E2 was 0.91. For both E2 and PG, selection of 5 or 7 days for the estimation of the midluteal mean level provided separation of within and between subject variance that was comparable with a LH-timed serum sample. These results indicate that daily saliva samples can be combined to clarify the interindividual differences in E2 and PG levels in premenopausal women, and that these interindividual differences may be greater than previously imagined.


Subject(s)
Estradiol/analysis , Progesterone/analysis , Saliva/chemistry , Adult , Female , Humans , Menstrual Cycle , Premenopause , Reference Values , Sensitivity and Specificity
7.
Phys Rev Lett ; 84(20): 4521-4, 2000 May 15.
Article in English | MEDLINE | ID: mdl-10990730

ABSTRACT

We propose an experiment that would demonstrate the dc and ac Josephson effects in two weakly linked Bose-Einstein condensates. We consider a time-dependent barrier, moving adiabatically across the trapping potential. The phase dynamics are governed by a "driven-pendulum" equation, as in current-driven superconducting Josephson junctions. At a critical velocity of the barrier (proportional to the critical tunneling current), there is a sharp transition between the dc and ac regimes. The signature is a sudden jump of a large fraction of the relative condensate population. Analytical results are compared with a numerical integration of the Gross-Pitaevskii equation, in an experimentally realistic situation.

8.
Phys Rev Lett ; 84(25): 5687-90, 2000 Jun 19.
Article in English | MEDLINE | ID: mdl-10991032

ABSTRACT

We show that particular configurations of intense off-resonant laser beams can give rise to an attractive 1/r interatomic potential between atoms located well within the laser wavelength. Such a "gravitational-like" interaction is shown to give stable Bose-Einstein condensates that are self-bound (without an additional trap) with unique scaling properties and measurably distinct signatures.

9.
Biochem J ; 325 ( Pt 1): 71-7, 1997 Jul 01.
Article in English | MEDLINE | ID: mdl-9224631

ABSTRACT

The internalization of [3H]iloprost, a prostacyclin analogue, was studied in human platelets by binding studies. After incubation with [3H]iloprost at 37 degrees C, addition of unlabelled ligand at either 37 degrees C or 4 degrees C caused dissociation of 74% and 52% of the bound ligand respectively, suggesting that a portion had been internalized. The percentage of [3H]iloprost bound at equilibrium to the surface (evaluated by acid treatment) at either 37 degrees C or 4 degrees C was markedly different (80% versus 25%). Internalization was dependent on time and on the ligand nature and concentration. Energy-depleting agents (dinitrophenol and 2-deoxyglucose) completely inhibited internalization, whereas probenecid (inhibitor of organic anion transporters) did not affect it significantly. Subcellular fractionation indicated that, at 4 degrees C or in the absence of ligand, most of the receptor was present in membrane fractions (pellet at 27000 or 105000 g), whereas, when platelets were preincubated at 37 degrees C with iloprost, the receptor was found mainly in the cytosolic fraction. In platelets preincubated with iloprost at 4 degrees C, two classes of binding sites were present, whereas after preincubation at 37 degrees C only the lower-affinity sites were detected. After exposure to the agonist, iloprost-induced inhibition of platelet aggregation and activation of adenylate cyclase and cAMP production were significantly lower. Taken together, these data demonstrate that human platelets can internalize a high-affinity binding site for iloprost, presumably the prostacyclin receptor.


Subject(s)
Blood Platelets/metabolism , Receptors, Prostaglandin/metabolism , Adenylyl Cyclases/blood , Binding, Competitive , Cell Membrane/metabolism , Down-Regulation , Epoprostenol/blood , Humans , Iloprost/blood , Iloprost/pharmacology , In Vitro Techniques , Infant, Newborn , Kinetics , Platelet Aggregation , Receptors, Epoprostenol , Receptors, Prostaglandin/biosynthesis , Subcellular Fractions/metabolism
10.
Gene ; 180(1-2): 145-50, 1996 Nov 21.
Article in English | MEDLINE | ID: mdl-8973359

ABSTRACT

The in vitro amplification method for heterologous gene expression in mammalian cells is based on the stable transfection of cells with long, linear DNA molecules having several copies of complete expression units, coding for the gene of interest, linked to one terminal unit, coding for the selectable marker. DNA concatenamers containing additional expression units can also be prepared: we exploited this feature by co-polymerizing expression units coding for granulocyte colony-stimulating factor (G-CSF) with cassettes for dihydrofolate reductase (DHFR) and for neomycin (Nm) resistance, as selectable markers. We were thus able to obtain high level production of G-CSF in chinese hamster ovary (CHO) dhfr- cells by combining in vitro amplification to just one step of in vivo amplification. This approach required a considerably shorter time than the classical, stepwise amplification by methotrexate.


Subject(s)
Cloning, Molecular/methods , Granulocyte Colony-Stimulating Factor/genetics , Nucleic Acid Amplification Techniques , Animals , CHO Cells , Cricetinae , DNA, Complementary , Granulocyte Colony-Stimulating Factor/biosynthesis , Humans , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/genetics , Simian virus 40/genetics , Tetrahydrofolate Dehydrogenase/genetics
13.
Hum Mol Genet ; 3(11): 1957-64, 1994 Nov.
Article in English | MEDLINE | ID: mdl-7874112

ABSTRACT

We describe the cloning and characterization of a new human Xq13 gene (XH2), extending over a 220 kb genomic stretch between MNK and DXS56. The gene, which undergoes X-inactivation, contains a 4 kb open reading frame and encodes a putative NTP-binding nuclear protein homologous to several members of the helicase II superfamily. The murine homologue maps to the syntenic genetic interval, between Pgk1 and Xist. In situ hybridization studies in mouse reveal precocious, widespread expression of the murine homologue of XH2 at early stages of embryogenesis, and more restricted expression during late developmental stages and at birth. XH2 is a new member of an expanding family of proven and putative helicases, sharing six conserved, collinear domains. In particular, the XH2 protein shows homology with yeast RAD54. Type II helicases have been implicated in nucleotide excision repair and the initiation of transcription. This new gene, represents a potential candidate for several genetic disorders mapped to human Xq13.


Subject(s)
Cloning, Molecular , DNA Helicases/genetics , Nuclear Proteins/genetics , X Chromosome , Amino Acid Sequence , Animals , Base Sequence , Chromosome Mapping , Humans , Hybrid Cells , In Situ Hybridization , Mice , Molecular Sequence Data , Polymerase Chain Reaction , X-linked Nuclear Protein
14.
Phys Rev Lett ; 72(20): 3230-3233, 1994 May 16.
Article in English | MEDLINE | ID: mdl-10056140
15.
J Pharmacol Exp Ther ; 268(1): 159-66, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8301553

ABSTRACT

The role of Ca++ as an intracellular messenger in leukotriene (LT)D4-induced muscle contraction was investigated by measuring force development and elevation in cytosolic Ca++ concentration simultaneously in strips of guinea pig ileal longitudinal muscle loaded with the fluorescent calcium indicator Fura 2. Upon addition of LTD4, a simultaneous increase in tension and cytosolic calcium concentration, [Ca++]i, was observed. Cumulative applications of LTD4 induced concentration-dependent increases in both muscle tension and [Ca++]i, being the half-maximal effect reached at approximately 6 to 9 nM. A statistically significant positive correlation (r = 0.993, P < .001) exists between the two parameters examined. Removal of calcium in the bathing solution, accompanied by addition of 7.5 mM EGTA, completely prevented any increase in either calcium levels or force development, thus indicating a role for Ca++ influx, rather than a release from intracellular stores. All of the LTD4 antagonists tested were able to counteract the effect of the leukotriene on both [Ca++]i and tension increase. However, although LY171883 shifted both of the LTD4 curves to the right in a parallel fashion, FPL 55712 and ICI 198,615 behaved as non-competitive antagonists in reversing the effect of LTD4 on [Ca++]i and tension. Thus, these results strongly suggest that changes in muscle tension induced by LTD4 are attributable to changes in cytosolic free Ca++ concentrations in guinea pig ileum.


Subject(s)
Calcium/metabolism , Leukotriene D4/pharmacology , Muscle Contraction , Muscle, Smooth/drug effects , Animals , Cytosol/drug effects , Cytosol/metabolism , Guinea Pigs , Histamine/pharmacology , Ileum , In Vitro Techniques , Male , Muscle Contraction/drug effects , Muscle, Smooth/physiology , Second Messenger Systems
16.
Biochem Pharmacol ; 44(7): 1411-5, 1992 Oct 06.
Article in English | MEDLINE | ID: mdl-1329767

ABSTRACT

We have identified and characterized two different subclasses of binding site for the novel peptido-leukotriene (LT) antagonist, [3H]ICI 198,615, in membranes from human lung parenchyma using a receptor-ligand assay. This novel compound is representative of a new class of LT receptor antagonists and it has been demonstrated to be several orders of magnitude more potent and selective than most other LT antagonists described to date. The binding of [3H]ICI 198,615 is rapid, specific and saturable. Equilibrium was reached within 5-10 min. Non linear fitting of dissociation time courses has revealed the presence of two different components (K(off)1 = 8.3 +/- 6.8 x 10(-4) sec-1 and K(off)2 = 0.79 +/- 1.66 x 10(-3) sec-1) of the kinetic curves, suggesting heterogeneity of the binding sites. Computer analysis of equilibrium binding data obtained at 25 degrees results in a model with two classes of binding sites, a high affinity-low capacity class with Kd1 = 0.024 +/- 0.014 nM and Bmax1 = 0.015 +/- 0.004 pmol/mg protein and a low affinity-high capacity class with Kd2 = 6326 +/- 3859 nM and Bmax2 = 473 +/- 383 pmol/mg protein. In competition studies, LTD4 was also found to interact with two classes of binding site (Kd1 = 0.016 +/- 0.008 nM and Kd2 = 15195 +/- 8965 nM). On the contrary, LTE4 and LTC4 were found to interact with a homogeneous class of sites only with Kd = 7466 +/- 4629 nM and Kd = 428 +/- 73 nM, respectively. Furthermore, we have evaluated the effect of a number of LT antagonists on the binding of [3H]ICI 198,615. Ro 24-5913 (Kd = 3.0 +/- 2.1 nM), FPL55712 (Kd = 4945 +/- 2868 nM), LY171883 (Kd = 19628 +/- 12365 nM), SKF 104353 (Kd = 74.2 +/- 46 nM) and its enantiomer SKF 104373 (Kd = 13627 +/- 6813 nM) were found to interact with a single class of binding sites. The present studies indicate a heterogeneity of binding sites for ICI 198,615 in membranes from human lung parenchyma and that ICI 198,615 is a very potent and selective antagonist of LTD4 receptors in this tissue.


Subject(s)
Indazoles/metabolism , Lung/metabolism , SRS-A/metabolism , Asthma/drug therapy , Asthma/metabolism , Binding Sites , Chromones/pharmacology , Dicarboxylic Acids/pharmacology , Humans , Indazoles/antagonists & inhibitors , Indazoles/pharmacology , Kinetics , Receptors, Immunologic/drug effects , Receptors, Leukotriene , SRS-A/antagonists & inhibitors , Software , Thiazoles/pharmacology
17.
Neuroreport ; 3(7): 601-4, 1992 Jul.
Article in English | MEDLINE | ID: mdl-1384767

ABSTRACT

In order to investigate the effects of ageing on the cerebral receptors for calcitonin (CT), we used an in vitro autoradiographic method to study the distribution of the binding sites for eel CT (eCT) in young and old rat brain. The inhibitory action of eCT on adenylyl-cyclase (AC) activity upon isolated brain cell membranes was also evaluated. The results show area-specific reduction of binding particularly in the hypothalamus and pons medulla of the old rat. The inhibitory action of eCT on AC activity was significantly reduced in the same areas, whereas in the striatum and mesencephalon no changes were observed. The parallel decrease of binding of eCT and of the inhibitory action of eCT on AC in ageing may represent a functional decline of neuronal activities during ageing.


Subject(s)
Adenylyl Cyclases/metabolism , Aging/metabolism , Brain/metabolism , Calcitonin/metabolism , Receptors, Cell Surface/metabolism , 1-Methyl-3-isobutylxanthine/pharmacology , Animals , Autoradiography , Brain/growth & development , Calcitonin/pharmacology , Carbon Radioisotopes , Cyclic AMP/metabolism , Iodine Radioisotopes , Kinetics , Male , Organ Specificity , Rats , Rats, Wistar , Receptors, Calcitonin , Tritium
18.
Pharmacol Res ; 25(2): 195-202, 1992.
Article in English | MEDLINE | ID: mdl-1635897

ABSTRACT

The present study has investigated the effect of prostaglandins and PAF on the contractility of the bovine ciliary muscle, a tissue involved in the control of aqueous outflow. The results show that the prostaglandins tested (PGI2, its stable analogue Iloprost, PGE2, PGE1, and PGF2 alpha) as well as PAF, were able to contract the ciliary muscle, although with different potencies and efficacies. PGI2 and Iloprost displayed parallel dose-effect curves with upper plateaus that did not differ significantly; however, PGI2 was slightly more potent than Iloprost. This is at variance with what is observed at the level of the platelet prostacyclin receptor. PGF2 alpha was equipotent with the PGEs tested, with a maximal effect not different from either PGI2 or PGEs. PAF was the most efficacious of the compounds tested.


Subject(s)
Muscle Contraction/drug effects , Muscle, Smooth/drug effects , Platelet Activating Factor/pharmacology , Prostaglandins/pharmacology , Animals , Cattle , Ciliary Body/metabolism , Dose-Response Relationship, Drug , In Vitro Techniques
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