1,277 research outputs found
Simulator evaluation of optimal thrust management/fuel conservation strategies for airbus aircraft on short haul routes
The feasibility of incorporating optimal concepts into a practical system was determined. Various earlier theoretical analyses were confirmed, and insight was gained into the sensitivity of fuel conservation strategies to nonlinear and second order aerodynamic and engine characteristics. In addition to the investigation of optimal trajectories the study ascertained combined fuel savings by utilizing various procedure-oriented improvements such as delayed flap/decelerating approaches and great circle navigation
Modulation of Natural Killer Cell Cytotoxicity in Human Cytomegalovirus Infection: The Role of Endogenous Class I Major Histocompatibility Complex and a Viral Class I Homolog
Natural killer (NK) cells have been implicated in early immune responses against certain viruses, including cytomegalovirus (CMV). CMV causes downregulation of class I major histocompatibility complex (MHC) expression in infected cells; however, it has been proposed that a class I MHC homolog encoded by CMV, UL18, may act as a surrogate ligand to prevent NK cell lysis of CMV-infected cells. In this study, we examined the role of UL18 in NK cell recognition and lysis using fibroblasts infected with either wild-type or UL18 knockout CMV virus, and by using cell lines transfected with the UL18 gene. In both systems, the expression of UL18 resulted in the enhanced killing of target cells. We also show that the enhanced killing is due to both UL18-dependent and -independent mechanisms, and that the killer cell inhibitory receptors (KIRs) and CD94/NKG2A inhibitory receptors for MHC class I do not play a role in affecting susceptibility of CMV-infected fibroblasts to NK cell–mediated cytotoxicity
Recommended from our members
Hypoimmunogenic Derivatives of Induced Pluripotent Stem Cells Evade Immune Rejection in Fully Immunocompetent Allogeneic Recipients
Atomic-scale structure of the SrTiO3(001)-c(6x2) reconstruction: Experiments and first-principles calculations
The c(6x2) is a reconstruction of the SrTiO3(001) surface that is formed
between 1050-1100oC in oxidizing annealing conditions. This work proposes a
model for the atomic structure for the c(6x2) obtained through a combination of
results from transmission electron diffraction, surface x-ray diffraction,
direct methods analysis, computational combinational screening, and density
functional theory. As it is formed at high temperatures, the surface is complex
and can be described as a short-range ordered phase featuring microscopic
domains composed of four main structural motifs. Additionally, non-periodic
TiO2 units are present on the surface. Simulated scanning tunneling microscopy
images based on the electronic structure calculations are consistent with
experimental images
Ly49H signaling through DAP10 is essential for optimal natural killer cell responses to mouse cytomegalovirus infection
The activating natural killer (NK) cell receptor Ly49H recognizes the mouse cytomegalovirus (MCMV) m157 glycoprotein expressed on the surface of infected cells and is required for protection against MCMV. Although Ly49H has previously been shown to signal via DAP12, we now show that Ly49H must also associate with and signal via DAP10 for optimal function. In the absence of DAP12, DAP10 enables Ly49H-mediated killing of m157-bearing target cells, proliferation in response to MCMV infection, and partial protection against MCMV. DAP10-deficient Ly49H+ NK cells, expressing only Ly49H–DAP12 receptor complexes, are partially impaired in their ability to proliferate during MCMV infection, display diminished ERK1/2 activation, produce less IFN-γ upon Ly49H engagement, and demonstrate reduced control of MCMV infection. Deletion of both DAP10 and DAP12 completely abrogates Ly49H surface expression and control of MCMV infection. Thus, optimal NK cell–mediated immunity to MCMV depends on Ly49H signaling through both DAP10 and DAP12
Activation of Prp28 ATPase by Phosphorylated Npl3 at a Critical Step of Spliceosome Remodeling
Splicing, a key step in the eukaryotic gene-expression pathway, converts precursor messenger RNA (pre-mRNA) into mRNA by excising introns and ligating exons. This task is accomplished by the spliceosome, a macromolecular machine that must undergo sequential conformational changes to establish its active site. Each of these major changes requires a dedicated DExD/H-box ATPase, but how these enzymes are activated remain obscure. Here we show that Prp28, a yeast DEAD-box ATPase, transiently interacts with the conserved 5\u27 splice-site (5\u27SS) GU dinucleotide and makes splicing-dependent contacts with the U1 snRNP protein U1C, and U4/U6.U5 tri-snRNP proteins, Prp8, Brr2, and Snu114. We further show that Prp28\u27s ATPase activity is potentiated by the phosphorylated Npl3, but not the unphosphorylated Npl3, thus suggesting a strategy for regulating DExD/H-box ATPases. We propose that Npl3 is a functional counterpart of the metazoan-specific Prp28 N-terminal region, which can be phosphorylated and serves as an anchor to human spliceosome
A Surface Reconstruction with a Fractional Hole: LaAlO (001)
The structure of the reconstruction of
LaAlO (001) has been determined using transmission electron diffraction
combined with direct methods. The structure is relatively simple, consisting of
a lanthanum oxide termination with one lanthanum cation vacancy per surface
unit cell. The electronic structure is unusual since a fractional number of
holes or atomic occupancies per surface unit cell are required to achieve
charge neutrality. Density functional calculations indicate that the charge
compensation mechanism occurs by means of highly delocalized holes. The surface
contains no oxygen vacancies and with a better than 99% confidence level, the
holes are not filled with hydrogen. The reconstruction can be understood in
terms of expulsion of the more electropositive cation from the surface followed
by an increased covalency between the remaining surface lanthanum atoms and
adjacent oxygen atoms.Comment: 4 Pages, 3 Figure
1938: Abilene Christian College Bible Lectures - Full Text
Delivered in the Auditorium of Abilene Christian College, February, 1938 Abilene, Texas.
Published October, 1939
PRICE, $1.00
FIRM FOUNDATION PUBLISHING HOUSE
Austin, Texas
- …