557 research outputs found
First Performance Results of a New Field-Widened Spatial Heterodyne Spectrometer for Geocoronal Hα Research
A new, high-resolution ïŹeld-widened spatial heterodyne spectrometer (FW-SHS) designed to observe geocoronal Balmer α (Hα, 6563 Ă
) emission was installed at Pine Bluff Observatory (PBO) near Madison, Wisconsin. FW-SHS observations were compared with an already well-characterized dual-etalon Fabry-Perot Interferometer (PBO FPI) optimized for Hα, also at PBO. The FW-SHS is a robust Fourier transform instrument that combines a large throughput advantage with high spectral resolution and a relatively long spectral baseline (~10 times that of the PBO FPI) in a compact, versatile instrument with no moving parts.Coincident Hα observations by FW-SHS and PBO FPI were obtained over similar integration times, resolving powers (~67,000 and 80,000 at Hα) and ïŹelds of view (1.8° and 1.4°, respectively). First light FW-SHS observations of Hα intensity and temperature (Doppler width) versus viewing geometry (shadow altitude) show excellent relative agreement with the geocoronal observations previously obtained at PBO by FPI. The FW-SHS has a 640 km/s (14 Ă
) spectral band pass and is capable of determining geocoronal Hα Doppler shifts on the order of 100 m/s with a temporal resolution on the order of minutes. These characteristics make the FW-SHS well suited for spectroscopic studies of relatively faint (~12â2 R), diffuse-source geocoronal Hα emission from EarthËs upper thermosphere and exosphere and the interstellar medium in our Galaxy. Current and future FW-SHS observations extend long-term geocoronal hydrogen observation data sets already spanning three solar minima. This paper describes the FW-SHS ïŹrst light performance and Hα observational results collected from observing nights across 2013 and 2014
Capacitance fluctuations causing channel noise reduction in stochastic Hodgkin-Huxley systems
Voltage-dependent ion channels determine the electric properties of axonal
cell membranes. They not only allow the passage of ions through the cell
membrane but also contribute to an additional charging of the cell membrane
resulting in the so-called capacitance loading. The switching of the channel
gates between an open and a closed configuration is intrinsically related to
the movement of gating charge within the cell membrane. At the beginning of an
action potential the transient gating current is opposite to the direction of
the current of sodium ions through the membrane. Therefore, the excitability is
expected to become reduced due to the influence of a gating current. Our
stochastic Hodgkin-Huxley like modeling takes into account both the channel
noise -- i.e. the fluctuations of the number of open ion channels -- and the
capacitance fluctuations that result from the dynamics of the gating charge. We
investigate the spiking dynamics of membrane patches of variable size and
analyze the statistics of the spontaneous spiking. As a main result, we find
that the gating currents yield a drastic reduction of the spontaneous spiking
rate for sufficiently large ion channel clusters. Consequently, this
demonstrates a prominent mechanism for channel noise reduction.Comment: 18 page
Co-Evolution of quasispecies: B-cell mutation rates maximize viral error catastrophes
Co-evolution of two coupled quasispecies is studied, motivated by the
competition between viral evolution and adapting immune response. In this
co-adaptive model, besides the classical error catastrophe for high virus
mutation rates, a second ``adaptation-'' catastrophe occurs, when virus
mutation rates are too small to escape immune attack. Maximizing both regimes
of viral error catastrophes is a possible strategy for an optimal immune
response, reducing the range of allowed viral mutation rates to a minimum. From
this requirement one obtains constraints on B-cell mutation rates and receptor
lengths, yielding an estimate of somatic hypermutation rates in the germinal
center in accordance with observation.Comment: 4 pages RevTeX including 2 figure
Tilt Texture Domains on a Membrane and Chirality induced Budding
We study the equilibrium conformations of a lipid domain on a planar fluid
membrane where the domain is decorated by a vector field representing the tilt
of the stiff fatty acid chains of the lipid molecules, while the surrounding
membrane is fluid and structureless. The inclusion of chirality in the bulk of
the domain induces a novel budding of the membrane, which preempts the budding
induced by a decrease in interfacial tension.Comment: 5 pages, 3 figure
String-like Clusters and Cooperative Motion in a Model Glass-Forming Liquid
A large-scale molecular dynamics simulation is performed on a glass-forming
Lennard-Jones mixture to determine the nature of dynamical heterogeneities
which arise in this model fragile liquid. We observe that the most mobile
particles exhibit a cooperative motion in the form of string-like paths
(``strings'') whose mean length and radius of gyration increase as the liquid
is cooled. The length distribution of the strings is found to be similar to
that expected for the equilibrium polymerization of linear polymer chains.Comment: 6 pages of RevTex, 6 postscript figures, uses epsf.st
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Overview of mathematical approaches used to model bacterial chemotaxis II: bacterial populations
We review the application of mathematical modeling to understanding the behavior of populations of chemotactic bacteria. The application of continuum mathematical models, in particular generalized KellerâSegel models, is discussed along with attempts to incorporate the microscale (individual) behavior on the macroscale, modeling the interaction between different species of bacteria, the interaction of bacteria with their environment, and methods used to obtain experimentally verified parameter values. We allude briefly to the role of modeling pattern formation in understanding collective behavior within bacterial populations. Various aspects of each model are discussed and areas for possible future research are postulated
T Cell-Intrinsic and -Extrinsic Contributions of the IFNAR/STAT1-Axis to Thymocyte Survival
STAT1 is an essential part of interferon signaling, and STAT1-deficiency results in heightened susceptibility to infections or autoimmunity in both mice and humans. Here we report that mice lacking the IFNα/ÎČ-receptor (IFNAR1) or STAT1 display impaired deletion of autoreactive CD4+CD8+-T-cells. Strikingly, co-existence of WT T cells restored thymic elimination of self-reactive STAT1-deficient CD4+CD8+-T cells. Analysis of STAT1-deficient thymocytes further revealed reduced Bim expression, which was restored in the presence of WT T cells. These results indicate that type I interferons and STAT1 play an important role in the survival of MHC class I-restricted T cells in a T cell intrinsic and non-cell intrinsic manner that involves regulation of Bim expression through feedback provided by mature STAT1-competent T cells
Ribosome Display Selection of a Murine IgG1 Fab Binding Affibody Molecule Allowing Species Selective Recovery Of Monoclonal Antibodies
Affinity reagents recognizing constant parts of antibody molecules are invaluable tools in immunotechnology applications, including purification, immobilization, and detection of immunoglobulins. In this article, murine IgG1, the primary isotype of monoclonal antibodies (mAbs) was used as target for selection of novel binders from a combinatorial ribosome display (RD) library of 1011 affibody molecules. Four rounds of selection using three different mouse IgG1 mAbs as alternating targets resulted in the identification of binders with broad mIgG1 recognition and dissociation constants (KD) in the low nanomolar to low micromolar range. For one of the binders, denoted Zmab25, competition in binding to full length mIgG1 by a streptococcal protein G (SPG) fragment and selective affinity capture of mouse IgG1 Fab fragments after papain cleavage of a full mAb suggest that an epitope functionally overlapping with the SPG-binding site in the CH1 domain of mouse IgG1 had been addressed. Interestingly, biosensor-based binding experiments showed that neither human IgG1 nor bovine Ig, the latter present in fetal bovine serum (FBS) was recognized by Zmab25. This selective binding profile towards murine IgG1 was successfully exploited in species selective recovery of two different mouse mAbs from complex samples containing FBS, resembling a hybridoma culture supernatant
The Kinetics of Early T and B Cell Immune Recovery after Bone Marrow Transplantation in RAG-2-Deficient SCID Patients
The kinetics of T and B cell immune recovery after bone marrow transplantation (BMT) is affected by many pre- and post-transplant factors. Because of the profoundly depleted baseline T and B cell immunity in recombination activating gene 2 (RAG-2)-deficient severe combined immunodeficiency (SCID) patients, some of these factors are eliminated, and the immune recovery after BMT can then be clearly assessed. This process was followed in ten SCID patients in parallel to their associated transplant-related complications. Early peripheral presence of T and B cells was observed in 8 and 4 patients, respectively. The latter correlated with pre-transplant conditioning therapy. Cells from these patients carried mainly signal joint DNA episomes, indicative of newly derived B and T cells. They were present before the normalization of the T cell receptor (TCR) and the B cell receptor (BCR) repertoire. Early presentation of the ordered TCR gene rearrangements after BMT occurred simultaneously, but this pattern was heterogeneous over time, suggesting different and individual thymic recovery processes. Our findings early after transplant could suggest the long-term patients' clinical outcome. Early peripheral presence of newly produced B and T lymphocytes from their production and maturation sites after BMT suggests donor stem cell origin rather than peripheral expansion, and is indicative of successful outcome. Peripheral detection of TCR excision circles and kappa-deleting recombination excision circles in RAG-2-deficient SCID post-BMT are early markers of T and B cell reconstitution, and can be used to monitor outcome and tailor specific therapy for patients undergoing BMT
Phenotypic Characterization of Autoreactive B CellsâCheckpoints of B Cell Tolerance in Patients with Systemic Lupus Erythematosus
DNA-reactive B cells play a central role in systemic lupus erythematosus (SLE); DNA antibodies precede clinical disease and in established disease correlate with renal inflammation and contribute to dendritic cell activation and high levels of type 1 interferon. A number of central and peripheral B cell tolerance mechanisms designed to control the survival, differentiation and activation of autoreactive B cells are thought to be disturbed in patients with SLE. The characterization of DNA-reactive B cells has, however, been limited by their low frequency in peripheral blood. Using a tetrameric configuration of a peptide mimetope of DNA bound by pathogenic anti-DNA antibodies, we can identify B cells producing potentially pathogenic DNA-reactive antibodies. We, therefore, characterized the maturation and differentiation states of peptide, (ds) double stranded DNA cross-reactive B cells in the peripheral blood of lupus patients and correlated these with clinical disease activity. Flow cytometric analysis demonstrated a significantly higher frequency of tetramer-binding B cells in SLE patients compared to healthy controls. We demonstrated the existence of a novel tolerance checkpoint at the transition of antigen-naĂŻve to antigen-experienced. We further demonstrate that patients with moderately active disease have more autoreactive B cells in both the antigen-naĂŻve and antigen-experienced compartments consistent with greater impairment in B cell tolerance in both early and late checkpoints in these patients than in patients with quiescent disease. This methodology enables us to gain insight into the development and fate of DNA-reactive B cells in individual patients with SLE and paves the way ultimately to permit better and more customized therapies
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