9,434 research outputs found
Generalized pairwise z-complementary codes
An approach to generate generalized pairwise Z-complementary (GPZ) codes, which works in pairs in order to offer a zero correlation zone (ZCZ) in the vicinity of zero phase shift and fit extremely well in power efficient quadrature carrier modems, is introduced in this letter. Each GPZ code has MK sequences, each of length 4NK, whereMis the number of Z-complementary mates,
K is a factor to perform Walsh–Hadamard expansions, and N is the sequence length of the Z-complementary code. The proposed GPZ codes include the generalized pairwise complementary (GPC)codes as special cases
Observation of the Presuperfluid Regime in a Two-Dimensional Bose Gas
In complementary images of coordinate-space and momentum-space density in a
trapped 2D Bose gas, we observe the emergence of pre-superfluid behavior. As
phase-space density increases toward degenerate values, we observe a
gradual divergence of the compressibility from the value predicted by
a bare-atom model, . grows to 1.7 before
reaches the value for which we observe the sudden emergence of a spike
at in momentum space. Momentum-space images are acquired by means of a 2D
focusing technique. Our data represent the first observation of non-meanfield
physics in the pre-superfluid but degenerate 2D Bose gas.Comment: Replace with the version appeared in PR
Tailored design of NKT-stimulatory glycolipids for polarization of immune responses.
Natural killer T (NKT) cell is a distinct population of T lymphocytes that can rapidly release massive amount of Th1 and Th2 cytokines upon the engagement of their T cell receptor with glycolipids presented by CD1d. The secreted cytokines can promote cell-mediated immunity to kill tumor cells and intracellular pathogens, or suppress autoreactive immune cells in autoimmune diseases. Thus, NKT cell is an attractive target for developing new therapeutics to manipulate immune system. The best-known glycolipid to activate NKT cells is α-galactosylceramide (α-GalCer), which has been used as a prototype for designing new NKT stimulatory glycolipids. Many analogues have been generated by modification of the galactosyl moiety, the acyl chain or the phytosphingosine chain of α-GalCer. Some of the analogues showed greater abilities than α-GalCer in polarizing immune responses toward Th1 or Th2 dominance. Among them, several analogues containing phenyl groups in the lipid tails were more potent in inducing Th1-skewed cytokines and exhibited greater anticancer efficacy than α-GalCer. Analyses of the correlation between structure and activity of various α-GalCer analogues on the activation of iNKT cell revealed that CD1d-glycolipid complexes interacted with the same population of iNKT cell expressing similar T-cell receptor Vβ as α-GalCer. On the other hand, those phenyl glycolipids with propensity for Th1 dominant responses showed greater binding avidity and stability than α-GalCer for iNKT T-cell receptor when complexed with CD1d. Thus, it is the avidity and stability of the ternary complexes of CD1d-glycolipid-iNKT TCR that dictate the polarity and potency of immune responses. These findings provide a key to the rationale design of immune modulating glycolipids with desirable Th1/Th2 polarity for clinical application. In addition, elucidation of α-GalCer-induced anergy, liver damage and accumulation of myeloid derived suppressor cells has offered explanation for its lacklustre anti-cancer activities in clinical trials. On other hand, the lack of such drawbacks in glycolipid analogues containing phenyl groups in the lipid tails of α-GalCer coupled with the greater binding avidity and stability of CD1d-glycolipid complex for iNKT T-cell receptor, account for their superior anti-cancer efficacy in tumor bearing mice. Further clinical development of these phenyl glycolipids is warranted
Design of multivariable feedback control systems via spectral assignment
The applicability of spectral assignment techniques to the design of multivariable feedback control systems was investigated. A fractional representation design procedure for unstable plants is presented and illustrated with an example. A computer aided design software package implementing eigenvalue/eigenvector design procedures is described. A design example which illustrates the use of the program is explained
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