548 research outputs found
Study of color suppressed modes
The color suppressed modes are
analyzed in perturbative QCD approach. We find that the dominant contribution
is from the non-factorizable diagrams. The branching ratios calculated in our
approach for agree with current experiments. By
neglecting the gluonic contribution, we predict the branching ratios of are at the comparable size of , but smaller than that of .Comment: revtex, 5 pages, axodraw.st
determination by
We investigate \ovar{B^0} \to D_s^- \pi^+ decay in perturbative QCD
approach which has recently been applied to meson decays. \ovar{B^0} \to
D_s^- \pi^+ decay (and its charge conjugated mode) can be one of the hopeful
modes to determine since it occurs through transition
only. We estimate both factorizable and non-factorizable contribution, and show
that the non-factorizable contribution is much less than the factorizable one.
Our calculation gives {BR}(\ovar{B^0} \to D_s^- \pi^+) = (50 \sim 70) \times
f_{Ds}^2|{V_{ub}}{V_{cs}}|^2.Comment: 12 pages, 3 figures, LaTeX2e with graphics packag
Semileptonic decays in the light-cone QCD sum rules
Semileptonic () decays are investigated systematically in the
light-cone QCD sum rules. Special emphasis is put on the LCSR calculation on
weak form factors with an adequate chiral current correlator, which turns out
to be particularly effective to control the pollution by higher twist
components of spectator mesons. The result for each channel depends on the
distribution amplitude of the the producing meson. The leading twist
distribution amplitudes of the related heavy mesons and charmonium are worked
out by a model approach in the reasonable way. A practical scenario is
suggested to understand the behavior of weak form factors in the whole
kinematically accessible ranges. The decay widths and branching ratios are
estimated for several () decay modes of current interest.Comment: 8 pages, talk given by the first arthur at 4th International
Conference on Flavor Physics (ICFP 2007), Beijing, China, Sept 24-28, 200
NMR and mutational identification of the collagen-binding site of the chaperone Hsp47.
Heat shock protein 47 (Hsp47) acts as a client-specific chaperone for collagen and plays a vital role in collagen maturation and the consequent embryonic development. In addition, this protein can be a potential target for the treatment of fibrosis. Despite its physiological and pathological importance, little is currently known about the collagen-binding mode of Hsp47 from a structural aspect. Here, we describe an NMR study that was conducted to identify the collagen-binding site of Hsp47. We used chicken Hsp47, which has higher solubility than its human counterpart, and applied a selective (15)N-labeling method targeting its tryptophan and histidine residues. Spectral assignments were made based on site-directed mutagenesis of the individual residues. By inspecting the spectral changes that were observed upon interaction with a trimeric collagen peptide and the mutational data, we successfully mapped the collagen-binding site in the B/C β-barrel domain and a nearby loop in a 3D-homology model based upon a serpin fold. This conclusion was confirmed by mutational analysis. Our findings provide a molecular basis for the design of compounds that target the interaction between Hsp47 and procollagen as therapeutics for fibrotic diseases
Possible Large Direct CP Violations in Charmless B-Decays
We discuss the perturbative QCD approach for the exclusive two body B-meson
decays to light mesons. We briefly review its ingredients and some important
theoretical issues on factorization approach. We show numerical results which
are compatible with present experimantal data for the charmless B-meson decays.
Specailly we predict the possibility of large direct CP violation effects in
and .
In the last section we investigate two methods to determine the weak phases
and from processes. We obtain bounds on
and from present experimental measurements.Comment: 18 pages, latex, 8 figures and 8 tables, typos corrected and added
more tables and references. Presented at the 3rd workshop on Higher
Luminosity B Factory, 6-7 August 2002, Kanagawa, Japan; Submitted to Phys.
Rev.
Branching ratios of decays in perturbative QCD approach
We study the rare decays , which can occur only via
annihilation type diagrams in the standard model. We calculate all of the four
modes, , in the framework of perturbative QCD approach
and give the branching ratios of the order about .Comment: 18 pages, 1 figure, Revte
Perturbative QCD analysis of decays
We study the first observed charmless modes, the
decays, in perturbative QCD formalism. The obtained branching ratios
are larger than
from QCD factorization. The comparison of the predicted magnitudes and phases
of the different helicity amplitudes, and branching ratios with experimental
data can test the power counting rules, the evaluation of annihilation
contributions, and the mechanism of dynamical penguin enhancement in
perturbative QCD, respectively.Comment: 14 pages, 2 tables, brief disscussion on hard sacle added, version to
appear in PR
Peptide exchange on MHC-I by TAPBPR is driven by a negative allostery release cycle.
Chaperones TAPBPR and tapasin associate with class I major histocompatibility complexes (MHC-I) to promote optimization (editing) of peptide cargo. Here, we use solution NMR to investigate the mechanism of peptide exchange. We identify TAPBPR-induced conformational changes on conserved MHC-I molecular surfaces, consistent with our independently determined X-ray structure of the complex. Dynamics present in the empty MHC-I are stabilized by TAPBPR and become progressively dampened with increasing peptide occupancy. Incoming peptides are recognized according to the global stability of the final pMHC-I product and anneal in a native-like conformation to be edited by TAPBPR. Our results demonstrate an inverse relationship between MHC-I peptide occupancy and TAPBPR binding affinity, wherein the lifetime and structural features of transiently bound peptides control the regulation of a conformational switch located near the TAPBPR binding site, which triggers TAPBPR release. These results suggest a similar mechanism for the function of tapasin in the peptide-loading complex
The transition form factors for semi-leptonic weak decays of in QCD sum rules
Within the Standard Model, we investigate the semi-leptonic weak decays of
. The various form factors of transiting to a single charmed
meson () are studied in the framework of the QCD sum rules.
These form factors fully determine the rates of the weak semi-leptonic decays
of and provide valuable information about the non-perturbative QCD
effects. Our results indicate that the decay rate of the semi-leptonic weak
decay mode is at order of .Comment: 28 pages, 6 figures, revised version to be published in Eur.Phys.J.
Study of Bc --> J/psi pi, etac pi decays with perturbative QCD approach
The Bc --> J/psi pi, etac pi decays are studied with the perturbative QCD
approach. It is found that form factors and branching ratios are sensitive to
the parameters w, v, f_J/psi and f_etac, where w and v are the parameters of
the charmonium wave functions for Coulomb potential and harmonic oscillator
potential, respectively, f_J/psi and f_etac are the decay constants of the
J/psi and etac mesons, respectively. The large branching ratios and the clear
signals of the final states make the Bc --> J/psi pi, etac pi decays to be the
prospective channels for measurements at the hadron collidersComment: 21 pages, revtex
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