Closed-flavor pi + J/psi and pi + Upsilon Cross Sections at Low Energies from Dipion Decays

The scale of low energy c-cbar and b-bbar cross sections on light hadrons is of great importance to searches for the quark gluon plasma using the heavy-quarkonium suppression signature. Unfortunately, little is known about these near-threshold cross sections at present, and recent theoretical estimates span many orders of magnitude. Here we use experimental data on the four observed closed-flavor heavy quarkonium hadronic decays psi' -> pi pi J/psi, Upsilon' -> pi pi Upsilon, Upsilon'' -> pi pi Upsilon and Upsilon'' -> pi pi Upsilon', combined with simple models of the transition amplitudes, to estimate the pion scattering cross sections of c-cbar and b-bbar mesons near threshold. Specifically we consider the closed-flavor reactions pi J/psi -> pi psi', pi Upsilon -> pi Upsilon', pi Upsilon -> pi Upsilon'' and pi Upsilon' -> pi Upsilon'' and their time-reversed analogues. Our results may be useful in constraining theoretical models of the strong interactions of heavy quarkonia, and can be systematically improved through future detailed studies of dipion decays, notably psi' -> pi pi J/psi and Upsilon'' -> pi pi Upsilon.Comment: 6 pages, 6 figure

Di-Pion Decays of Heavy Quarkonium in the Field Correlator Method

Mechanism of di-pion transitions $nS\to n'S\pi\pi(n=3,2; n'=2,1)$ in bottomonium and charmonium is studied with the use of the chiral string-breaking Lagrangian allowing for the emission of any number of $\pi(K,\eta),$ and not containing fitting parameters. The transition amplitude contains two terms, $M=a-b$, where first term (a) refers to subsequent one-pion emission: $\Upsilon(nS)\to\pi B\bar B^*\to\pi\Upsilon(n'S)\pi$ and second term (b) refers to two-pion emission: $\Upsilon(nS)\to\pi\pi B\bar B\to\pi\pi\Upsilon(n'S)$. The one-parameter formula for the di-pion mass distribution is derived, $\frac{dw}{dq}\sim$(phase space) $|\eta-x|^2$, where $x=\frac{q^2-4m^2_\pi}{q^2_{max}-4m^2_\pi},$ $q^2\equiv M^2_{\pi\pi}$. The parameter $\eta$ dependent on the process is calculated, using SHO wave functions and imposing PCAC restrictions (Adler zero) on amplitudes a,b. The resulting di-pion mass distributions are in agreement with experimental data.Comment: 62 pages,8 tables,7 figure

Ukupno harmoničko izobličenje i brzina prostorne modalne informacije za analizu haptičkog paralelnog gibanja

In this paper, two kinds of evaluation index for the haptic motion analysis in parallel multiple degrees–of–freedom (MDOF) system are proposed. At first, the spatial modal decomposition method based on discrete Fourier series expansion (DFS) is presented. Spatial modal information expresses a motion element that corresponds to a specific physical action. The spatial modal information can mathematically be defined by the Fourier coefficients. Then, this paper proposes the total harmonic distortion (THD) and the content rate of the haptic modal information as motion evaluation indexes. THD of the spatial modal information can evaluate the complexity of the human motion and/or the deformability of the contact environment. Content rate of the spatial modal information can evaluate the priority of motion element. Some experimental results on the bilateral motion control of a parallel five DOF haptic system are shown, in order to confirm the utility of the proposed indexes.U ovom radu predložena su dva indikatora vrednovanja haptičkog gibanja u paralelnom sustavu s više stupnjeva slobode. Prikazana je metoda prostorne modalne dekompozicije zasnovana na proširenom diskretnom Fourierovom redu. Prostorna modalna informacija predstavlja element koji odgovara specifičnoj fizikalnoj radnji. Prostorna modalna informacija matematički se može opisati koristeći Fourierove koeficijente. U ovom se radu kao indikatori za evaluaciju gibanja predlažu ukupno harmoničko izobličenje i brzina haptičke modalne informacije. Ukupnim harmoničkim izobličenjem prostorne modalne informacije može se ocijeniti kompleksnost ljudskog gibanja i/ili deformabilnost kontaktne okoline. Przina prostorne modalne informacije ocjenjuje prioritet elementa u gibanju. Kako bi se potvrdila korisnost predloženih indikatora vrednovanja prikazani su eksperimentalni rezultati dobiveni dvoosnim prostornim upravljanjem paralelnim haptičkim sustavom s pet stupnjeva slobode

Observation of the Hadronic Transitions Chi_{b 1,2}(2P) -> omega Upsilon(1S)

The CLEO Collaboration has observed the first hadronic transition among bottomonium (b bbar) states other than the dipion transitions among vector states, Upsilon(nS) -> pi pi Upsilon(mS). In our study of Upsilon(3S) decays, we find a significant signal for Upsilon(3S) -> gamma omega Upsilon(1S) that is consistent with radiative decays Upsilon(3S) -> gamma chi_{b 1,2}(2P), followed by chi_{b 1,2} -> omega Upsilon(1S). The branching ratios we obtain are Br(chi_{b1} -> omega Upsilon(1S) = 1.63 (+0.35 -0.31) (+0.16 -0.15) % and Br(chi_{b2} -> omega Upsilon(1S) = 1.10 (+0.32 -0.28) (+0.11 - 0.10)%, in which the first error is statistical and the second is systematic.Comment: submitted to XXI Intern'l Symp on Lepton and Photon Interact'ns at High Energies, August 2003, Fermila

The role of ubiquitination and hepatocyte growth factor-regulated tyrosine kinase substrate in the degradation of the adrenomedullin type I receptor

Calcitonin receptor-like receptor (CLR) and the receptor activity-modifying protein 2 (RAMP2) comprise a receptor for adrenomedullin (AM). Although it is known that AM induces internalization of CLR•RAMP2, little is known about the molecular mechanisms that regulate the trafficking of CLR•RAMP2. Using HEK and HMEC-1 cells, we observed that AM-induced activation of CLR•RAMP2 promoted ubiquitination of CLR. A mutant (CLRΔ9KR), lacking all intracellular lysine residues was functional and trafficked similar to the wild-type receptor, but was not ubiquitinated. Degradation of CLR•RAMP2 and CLRΔ9KR•RAMP2 was not dependent on the duration of AM stimulation or ubiquitination and occurred via a mechanism that was partially prevented by peptidase inhibitors. Degradation of CLR•RAMP2 was sensitive to overexpression of hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), but not to HRS knockdown, whereas CLRΔ9KR•RAMP2 degradation was unaffected. Overexpression, but not knockdown of HRS, promoted hyperubiquitination of CLR under basal conditions. Thus, we propose a role for ubiquitin and HRS in the regulation of AM-induced degradation of CLR•RAMP2

In-Cell Biochemistry Using NMR Spectroscopy

Biochemistry and structural biology are undergoing a dramatic revolution. Until now, mostly in vitro techniques have been used to study subtle and complex biological processes under conditions usually remote from those existing in the cell. We developed a novel in-cell methodology to post-translationally modify interactor proteins and identify the amino acids that comprise the interaction surface of a target protein when bound to the post-translationally modified interactors. Modifying the interactor proteins causes structural changes that manifest themselves on the interacting surface of the target protein and these changes are monitored using in-cell NMR. We show how Ubiquitin interacts with phosphorylated and non-phosphorylated components of the receptor tyrosine kinase (RTK) endocytic sorting machinery: STAM2 (Signal-transducing adaptor molecule), Hrs (Hepatocyte growth factor regulated substrate) and the STAM2-Hrs heterodimer. Ubiquitin binding mediates the processivity of a large network of interactions required for proper functioning of the RTK sorting machinery. The results are consistent with a weakening of the network of interactions when the interactor proteins are phosphorylated. The methodology can be applied to any stable target molecule and may be extended to include other post-translational modifications such as ubiquitination or sumoylation, thus providing a long-awaited leap to high resolution in cell biochemistry