667 research outputs found
Langerin-Heparin Interaction: Two Binding Sites for Small and Large Ligands as revealed by a combination of NMR Spectroscopy and Cross-Linking Mapping Experiments
Langerin is a C-type lectin present on Langerhans cells that mediates capture of pathogens in a carbohydrate-dependent manner, leading to subsequent internalization and elimination in the cellular organelles called Birbeck granules. This mechanism mediated by langerin was shown to constitute a natural barrier for HIV-1 particle transmission. Besides interacting specifically with high mannose and fucosylated neutral carbohydrate structures, langerin has the ability to bind sulfated carbohydrate ligands as 6-sulfated galactosides in the Ca2+ dependent binding site. Very recently langerin was demonstrated to interact with sulfated glycosaminoglycans (GAGs), in a Ca2+ independent way, resulting in the proposal of a new binding site for GAGs. Based on those results, we have conducted a structural study of the interactions of small heparin (HEP) like oligosaccharides with langerin in solution. Heparin-bead cross-linking experiments, an approach specifically designed to identify HEP/HS binding sites in proteins were first carried out and experimentally validated the previously proposed model for the interaction of Lg ECD with 6 kDa HEP. High-resolution NMR studies of a set of 8 synthetic HEP-like trisaccharides harboring different sulfation patterns demonstrated that all of them bound to langerin in a Ca2+ dependent way. The binding epitopes were determined by STD NMR and the bound conformations by transferred NOESY experiments. These experimental data were combined with docking and molecular dynamics and resulted in the proposal of a binding mode characterized by the coordination of calcium by the two equatorial hydroxyl groups OH3 and OH4 at the non-reducing end. The binding also includes the carboxylate group at the adjacent iduronate residue. Such epitope is shared by all the 8 ligands, explaining the absence of any impact on binding from their differences in substitution pattern. Finally, in contrast to the small trisaccharides, we demonstrated that a longer HEP-like hexasaccharide, bearing an additional O-sulfate group at the non-reducing end, which precludes binding to the Ca2+ site, interacts with langerin in the previously identified Ca2+ independent binding site
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A Task-based Support Architecture for Developing Point-of-care Clinical Decision Support Systems for the Emergency Department
Objectives: The purpose of this study was to create a task-based support architecture for developing clinical decision support systems (CDSSs) that assist physicians in making decisions at the point-of-care in the emergency department (ED). The backbone of the proposed architecture was established by a task-based emergency workflow model for a patient-physician encounter.
Methods: The architecture was designed according to an agent-oriented paradigm. Specifically, we used the O-MaSE (Organization-based Multi-agent System Engineering) method that allows for iterative translation of functional requirements into architectural components (e.g., agents). The agent-oriented paradigm was extended with ontology-driven design to implement ontological models representing knowledge required by specific agents to operate.
Results: The task-based architecture allows for the creation of a CDSS that is aligned with the task-based emergency workflow model. It facilitates decoupling of executable components (agents) from embedded domain knowledge (ontological models), thus supporting their interoperability, sharing, and reuse. The generic architecture was implemented as a pilot system, MET3-AE â a CDSS to help with the management of pediatric asthma exacerbation in the ED. The system was evaluated in a hospital ED.
Conclusions: The architecture allows for the creation of a CDSS that integrates support for all tasks from the task-based emergency workflow model, and interacts with hospital information systems. Proposed architecture also allows for reusing and sharing system components and knowledge across disease-specific CDSSs
OA011-03. Clusterin, a natural ligand of DC-SIGN present in human semen inhibits HIV capture and transmission by dendritic cells
International audiencen.
The roles of transparency and trust in the relationship between corruption and citizen satisfaction
Reducing corruption and improving citizen satisfaction are important aims of government, yet the link between these two policy aims has rarely been explored. This article reports a study into the roles played by transparency and trust in the relationship between governmental corruption and citizen satisfaction with public services. The study was based on data gathered in South Korea to evaluate a specific initiative that had sought to reduce corruption and increase citizen satisfaction with public works programmes. The data indicated that the relationship between corruption and satisfaction was moderated by transparency and partially mediated by trust.
Points for practitioners:
The study sheds light on the roles of transparency and trust in the relationship between corruption and citizen satisfaction with public services, and thus provides insights for developing policy aimed at curtailing corruption and improving satisfaction
The E00-110 experiment in Jefferson Lab's Hall A: Deeply Virtual Compton Scattering off the Proton at 6 GeV
We present final results on the photon electroproduction
() cross section in the deeply virtual Compton
scattering (DVCS) regime and the valence quark region from Jefferson Lab
experiment E00-110. Results from an analysis of a subset of these data were
published before, but the analysis has been improved which is described here at
length, together with details on the experimental setup. Furthermore,
additional data have been analyzed resulting in photon electroproduction cross
sections at new kinematic settings, for a total of 588 experimental bins.
Results of the - and -dependences of both the helicity-dependent and
helicity-independent cross sections are discussed. The -dependence
illustrates the dominance of the twist-2 handbag amplitude in the kinematics of
the experiment, as previously noted. Thanks to the excellent accuracy of this
high luminosity experiment, it becomes clear that the unpolarized cross section
shows a significant deviation from the Bethe-Heitler process in our kinematics,
compatible with a large contribution from the leading twist-2 DVCS term to
the photon electroproduction cross section. The necessity to include
higher-twist corrections in order to fully reproduce the shape of the data is
also discussed. The DVCS cross sections in this paper represent the final set
of experimental results from E00-110, superseding the previous publication.Comment: 48 pages, 32 figure
Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease
The transcription factor signal transducer and activator of transcription-1 (STAT1) plays a key role in immunity against mycobacterial and viral infections. Here, we characterize three human STAT1 germline alleles from otherwise healthy patients with mycobacterial disease. The previously reported L706S, like the novel Q463H and E320Q alleles, are intrinsically deleterious for both interferon gamma (IFNG)âinduced gamma-activating factorâmediated immunity and interferon alpha (IFNA)âinduced interferon-stimulated genes factor 3âmediated immunity, as shown in STAT1-deficient cells transfected with the corresponding alleles. Their phenotypic effects are however mediated by different molecular mechanisms, L706S affecting STAT1 phosphorylation and Q463H and E320Q affecting STAT1 DNA-binding activity. Heterozygous patients display specifically impaired IFNG-induced gamma-activating factorâmediated immunity, resulting in susceptibility to mycobacteria. Indeed, IFNA-induced interferon-stimulated genes factor 3âmediated immunity is not affected, and these patients are not particularly susceptible to viral disease, unlike patients homozygous for other, equally deleterious STAT1 mutations recessive for both phenotypes. The three STAT1 alleles are therefore dominant for IFNG-mediated antimycobacterial immunity but recessive for IFNA-mediated antiviral immunity at the cellular and clinical levels. These STAT1 alleles define two forms of dominant STAT1 deficiency, depending on whether the mutations impair STAT1 phosphorylation or DNA binding
Deeply Virtual Compton Scattering off the neutron
The present experiment exploits the interference between the Deeply Virtual
Compton Scattering (DVCS) and the Bethe-Heitler processes to extract the
imaginary part of DVCS amplitudes on the neutron and on the deuteron from the
helicity-dependent D cross section measured at =1.9
GeV and =0.36. We extract a linear combination of generalized parton
distributions (GPDs) particularly sensitive to , the least constrained
GPD. A model dependent constraint on the contribution of the up and down quarks
to the nucleon spin is deduced.Comment: Published in Phys. Rev. Let
Exclusive Neutral Pion Electroproduction in the Deeply Virtual Regime
We present measurements of the ep->ep pi^0 cross section extracted at two
values of four-momentum transfer Q^2=1.9 GeV^2 and Q^2=2.3 GeV^2 at Jefferson
Lab Hall A. The kinematic range allows to study the evolution of the extracted
hadronic tensor as a function of Q^2 and W. Results will be confronted with
Regge inspired calculations and GPD predictions. An intepretation of our data
within the framework of semi-inclusive deep inelastic scattering has also been
attempted
Scaling Tests of the Cross Section for Deeply Virtual Compton Scattering
We present the first measurements of the \vec{e}p->epg cross section in the
deeply virtual Compton scattering (DVCS) regime and the valence quark region.
The Q^2 dependence (from 1.5 to 2.3 GeV^2) of the helicity-dependent cross
section indicates the twist-2 dominance of DVCS, proving that generalized
parton distributions (GPDs) are accessible to experiment at moderate Q^2. The
helicity-independent cross section is also measured at Q^2=2.3 GeV^2. We
present the first model-independent measurement of linear combinations of GPDs
and GPD integrals up to the twist-3 approximation.Comment: 5 pages, 4 figures, 2 tables. Text shortened for publication.
References added. One figure remove
Internet-based medical education: a realist review of what works, for whom and in what circumstances
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