688 research outputs found
Semileptonic and Rare -meson transitions in a QCD relativistic potential model
Using a QCD relativistic potential model, previously applied to the
calculation of the heavy meson leptonic constants, we evaluate the form factors
governing the exclusive decays , and . In our approach the heavy meson is described as a
bound state, whose wave function is solution of the relativistic Salpeter
equation, with an instantaneous potential displaying Coulombic behaviour at
small distances and linear behaviour at large distances. The light vector meson
is described by using a vector current interpolating field, according to the
Vector Meson Dominance assumption. A Pauli-Villars regularized propagator is
assumed for the quarks not constituting the heavy meson. Our procedure allows
to avoid the description of the light meson in terms of wave function and
constituent quarks, and consequently the problem of boosting the light meson
wave function.
Assuming as an input the experimental results on , we
evaluate all the form factors describing the semileptonic and
rare transitions. The overall comparison with the data, whenever available, is
satisfactory.Comment: Latex, 19 pages, 3 figure
Phenomenological Bounds on B to Light Semileptonic Form Factors
The form factors for the weak currents between B and light mesons are studied
by relating them to the corresponding D form factors at q^2_{max} according to
HQET, by evaluating them at q^2=0 by QCD sum rules, and by assuming a polar q^2
dependence. The results found are consistent with the information obtained from
exclusive non-leptonic two-body decays and, with the only exception of A_1,
with lattice calculations.Comment: 8 LaTeX pages + 2 figures. Will appear in Mod. Phys. Lett.
Tackling dysfunction of mitochondrial bioenergetics in the brain
Oxidative phosphorylation (OxPhos) is the basic function of mitochondria, although the landscape of mitochondrial functions is continuously growing to include more aspects of cellular homeostasis. Thanks to the application of -omics technologies to the study of the OxPhos system, novel features emerge from the cataloging of novel proteins as mitochondrial thus adding details to the mitochondrial proteome and defining novel metabolic cellular interrelations, especially in the human brain. We focussed on the diversity of bioenergetics demand and different aspects of mitochondrial structure, functions, and dysfunction in the brain. Definition such as âmitoexomeâ, âmitoproteomeâ and âmitointeractomeâ have entered the field of âmitochondrial medicineâ. In this context, we reviewed several genetic defects that hamper the last step of aerobic metabolism, mostly involving the nervous tissue as one of the most prominent energy-dependent tissues and, as consequence, as a primary target of mitochondrial dysfunction. The dual genetic origin of the OxPhos complexes is one of the reasons for the complexity of the genotype-phenotype correlation when facing human diseases associated with mitochondrial defects. Such complexity clinically manifests with extremely heterogeneous symptoms, ranging from organ-specific to multisystemic dysfunction with different clinical courses. Finally, we briefly discuss the future directions of the multi-omics study of human brain disorders
Integrative organelle-based functional proteomics: in silico prediction of impaired functional annotations in SACS KO cell model
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an inherited neurodegenerative disease characterized by early-onset spasticity in the lower limbs, axonal-demyelinating sensorimotor peripheral neuropathy, and cerebellar ataxia. Our understanding of ARSACS (genetic basis, protein function, and disease mechanisms) remains partial. The integrative use of organelle-based quantitative proteomics and whole-genome analysis proposed in the present study allowed identifying the affected disease-specific pathways, upstream regulators, and biological functions related to ARSACS, which exemplify a rationale for the development of improved early diagnostic strategies and alternative treatment options in this rare condition that currently lacks a cure. Our integrated results strengthen the evidence for disease-specific defects related to bioenergetics and protein quality control systems and reinforce the role of dysregulated cytoskeletal organization in the pathogenesis of ARSACS
Nonleptonic Cabibbo Favoured -Decays and -Asymmetries for Charmed Final Hadron States in Isgur and Wise Theory
The Cabibbo allowed non-leptonic -decays in two hadrons are studied,
within the factorization hypothesis, in the framework of Isgur and Wise theory
for the matrix elements of the weak currents. The
symmetry relates to currents, which
have been measured in the semileptonic strange decays of charmed particles. By
assuming colour screening and allowing for invariant contributions from
the annihilation terms with charmed final states one is able to comply with the
present experimental knowledge.\\ The violating asymmetries in neutral
decays are given for charmed final states in terms of the angles. With
the central values found for the annihilation parameters there is a destructive
(constructive) interference between the direct and annihilation terms in the
Cabibbo allowed (doubly forbidden) amplitudes for the decays into
and so that they may be of the same order.
This would imply large asymmetries, for which however our present knowledge on
the amplitudes does not allow to predict even their sign.\\ We have better
confidence in our predictions for the charged final states than the neutral
ones and can draw the conclusion that the detection of the corresponding
asymmetries requires, at least, tagged neutral -particles.Comment: CERNTEX, 17 pages, DSF-92/23, INFN-NA-IV-92/2
Quantum Effects in Friedmann-Robertson-Walker Cosmologies
Electrodynamics for self-interacting scalar fields in spatially flat
Friedmann-Robertson-Walker space-times is studied. The corresponding one-loop
field equation for the expectation value of the complex scalar field in the
conformal vacuum is derived. For exponentially expanding universes, the
equations for the Bogoliubov coefficients describing the coupling of the scalar
field to gravity are solved numerically. They yield a non-local correction to
the Coleman-Weinberg effective potential which does not modify the pattern of
minima found in static de Sitter space. Such a correction contains a
dissipative term which, accounting for the decay of the classical configuration
in scalar field quanta, may be relevant for the reheating stage. The physical
meaning of the non-local term in the semiclassical field equation is
investigated by evaluating this contribution for various background field
configurations.Comment: 17 pages, plain TeX + 5 uuencoded figure
"Double troubleâ or digenic disorder in Complex I deficiency
Complex I (CI) deficiency is a defect of OXPHOS caused by mutations in the mitochondrial or nuclear genomes. To date disease-causing mutations have been reported in all mitochondrial-encoded subunits and 22 nuclear genes. In about 50% of the patients no mutations are found, suggesting that undiscovered factors are an important cause of disease.
In this study we report a consanguineous family from Southern Portugal with three affected children presenting with CI deficiency and 3-methylglutaconic aciduria type IV
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction
Background: Charcot-Marie-Tooth disease (CMT) type 4B3 (CMT4B3) is a rare form of genetic neuropathy associated with variants in the MTMR5/SBF1 gene. MTMR5/SBF1 is a pseudophosphatase predicted to regulate endo-lysosomal trafficking in tandem with other MTMRs. Although almost ubiquitously expressed, pathogenic variants primarily impact on the peripheral nervous system, corroborating the involvement of MTMR5/SBF1 and its molecular partners in Schwann cells-mediated myelinization. Case presentation: We report a case of severe CMT4B3 characterized by early-onset motor and axonal polyneuropathy in an Italian child in absence of any evidence of brain and spine MRI abnormalities or intellectual disability and with a biochemical profile suggestive of mitochondrial disease. Using an integrated approach combining both NGS gene panels and WES analysis, we identified two novel compound heterozygous missense variants in MTMR5/SBF1 gene, p.R763H (c.2291G > A) and p.G1064E (c.3194G > A). Studies in muscle identified partial defects of oxidative metabolism. Conclusion: We describe the first case of an early onset severe polyneuropathy with motor and axonal involvement, due to recessive variants in the MTMR5/SBF1 gene, with no evidence of brain and spine MRI abnormalities, intellectual disability, no clinical and neurophysiological evidences of distal sensory impairment, and rapid neuromuscular deterioration. This report suggests that MTMR5/SBF1 should be considered in cases of infantile-onset CMT with secondary mitochondrial dysfunction
New Measurement of the Relative Scintillation Efficiency of Xenon Nuclear Recoils Below 10 keV
Liquid xenon is an important detection medium in direct dark matter
experiments, which search for low-energy nuclear recoils produced by the
elastic scattering of WIMPs with quarks. The two existing measurements of the
relative scintillation efficiency of nuclear recoils below 20 keV lead to
inconsistent extrapolations at lower energies. This results in a different
energy scale and thus sensitivity reach of liquid xenon dark matter detectors.
We report a new measurement of the relative scintillation efficiency below 10
keV performed with a liquid xenon scintillation detector, optimized for maximum
light collection. Greater than 95% of the interior surface of this detector was
instrumented with photomultiplier tubes, giving a scintillation yield of 19.6
photoelectrons/keV electron equivalent for 122 keV gamma rays. We find that the
relative scintillation efficiency for nuclear recoils of 5 keV is 0.14, staying
constant around this value up to 10 keV. For higher energy recoils we measure a
value around 20%, consistent with previously reported data. In light of this
new measurement, the XENON10 experiment's results on spin-independent
WIMP-nucleon cross section, which were calculated assuming a constant 0.19
relative scintillation efficiency, change from cm to
cm for WIMPs of mass 100 GeV/c, and from
cm to cm for WIMPs of mass 30
GeV/c.Comment: 8 pages, 8 figure
- âŠ