243 research outputs found
The FCC-ee study: Progress and challenges
The FCC (Future Circular Collider) study represents a vision for the next
large project in high energy physics, comprising an 80-100 km tunnel that can
house a future 100 TeV hadron collider. The study also includes a high
luminosity e+e- collider operating in the centre-of-mass energy range of 90-350
GeV as a possible intermediate step, the FCC-ee. The FCC-ee aims at definitive
electro-weak precision measurements of the Z, W, H and top particles, and
search for rare phenomena. Although FCC-ee is based on known technology, the
goal performance in luminosity and energy calibration make it quite
challenging. During 2014 the study went through an exploration phase. The study
has now entered its second year and the aim is to produce a conceptual design
report during the next three to four years. We here report on progress since
the last IPAC conference.Comment: Poster presented at IPAC15,Richmond, VA, USA, May 201
Status of the Super-B factory Design
The SuperB international team continues to optimize the design of an
electron-positron collider, which will allow the enhanced study of the origins
of flavor physics. The project combines the best features of a linear collider
(high single-collision luminosity) and a storage-ring collider (high repetition
rate), bringing together all accelerator physics aspects to make a very high
luminosity of 10 cm sec. This asymmetric-energy collider
with a polarized electron beam will produce hundreds of millions of B-mesons at
the (4S) resonance. The present design is based on extremely low
emittance beams colliding at a large Piwinski angle to allow very low
without the need for ultra short bunches. Use of crab-waist
sextupoles will enhance the luminosity, suppressing dangerous resonances and
allowing for a higher beam-beam parameter. The project has flexible beam
parameters, improved dynamic aperture, and spin-rotators in the Low Energy Ring
for longitudinal polarization of the electron beam at the Interaction Point.
Optimized for best colliding-beam performance, the facility may also provide
high-brightness photon beams for synchrotron radiation applications
Energetic Protons and Deuterons Emitted Following μ⁻ Capture by ³He Nuclei
Spectra of energetic protons and deuterons emitted following negative muon capture from rest in 3He have been measured for the first time. Significant capture strength is observed at high energy transfers (mμ- Ev \u3e60 MeV) for the two-body and three-body breakup channels, indicative of the importance of nucleon-nucleon correlations and meson exchange currents in the capture process. A simple plane wave impulse approximation calculation reproduces the proton spectrum reasonably well, but underpredicts the deuteron rate at the highest energies by a large factor
Sequential phosphorylation of SLP-76 at tyrosine 173 is required for activation of T and mast cells.
Cooperatively assembled signalling complexes, nucleated by adaptor proteins, integrate information from surface receptors to determine cellular outcomes. In T and mast cells, antigen receptor signalling is nucleated by three adaptors: SLP-76, Gads and LAT. Three well-characterized SLP-76 tyrosine phosphorylation sites recruit key components, including a Tec-family tyrosine kinase, Itk. We identified a fourth, evolutionarily conserved SLP-76 phosphorylation site, Y173, which was phosphorylated upon T-cell receptor stimulation in primary murine and Jurkat T cells. Y173 was required for antigen receptor-induced phosphorylation of phospholipase C-γ1 (PLC-γ1) in both T and mast cells, and for consequent downstream events, including activation of the IL-2 promoter in T cells, and degranulation and IL-6 production in mast cells. In intact cells, Y173 phosphorylation depended on three, ZAP-70-targeted tyrosines at the N-terminus of SLP-76 that recruit and activate Itk, a kinase that selectively phosphorylated Y173 in vitro. These data suggest a sequential mechanism whereby ZAP-70-dependent priming of SLP-76 at three N-terminal sites triggers reciprocal regulatory interactions between Itk and SLP-76, which are ultimately required to couple active Itk to its substrate, PLC-γ1
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