272 research outputs found
Generalized quasi-Banach sequence spaces and measures of noncompactness
Given 0 < s ≤ 1 and ψ an s-convex function, s – ψ -sequence spaces are introduced. Several quasi-Banach sequence spaces are thus characterized as a particular case of s – ψ -spaces. For these spaces, new measures of noncompactness are also defined, related to the Hausdorff measure of noncompactness. As an application, compact sets in s – ψ -interpolation spaces of a quasi-Banach couple are studied.Dado 0 < s ? 1 e uma função s-convexa ?, os espaços de sequencias s – ? são introduzidos. Vários espaços quase-Banach de sequencias são assim caracterizados como um caso particular dos espaços s – ?. Para esses espaços novas medidas de não compacidade são também definidas, relacionadas a medida de não compacidade de Hausdorff. Como uma aplicação, conjuntos compactos nos espa, cos de interpolação s – ?, de um par quase-Banach são estudados.44345
Fine Mapping of the Interaction between C4b-Binding Protein and Outer Membrane Proteins LigA and LigB of Pathogenic Leptospira interrogans.
The complement system consists of more than 40 proteins that participate in the inflammatory response and in pathogen killing. Complement inhibitors are necessary to avoid the excessive consumption and activation of this system on host cells. Leptospirosis is a worldwide zoonosis caused by spirochetes from the genus Leptospira. Pathogenic leptospires are able to escape from complement activation by binding to host complement inhibitors Factor H [FH] and C4b-binding protein (C4BP) while non-pathogenic leptospires are rapidly killed in the presence of fresh serum. In this study, we demonstrate that complement control protein domains (CCP) 7 and 8 of C4BP α-chain interact with the outer membrane proteins LcpA, LigA and LigB from the pathogenic leptospire L. interrogans. The interaction between C4BP and LcpA, LigA and LigB is sensitive to ionic strength and inhibited by heparin. We fine mapped the LigA and LigB domains involved in its binding to C4BP and heparin and found that both interactions are mediated through the bacterial immunoglobulin-like (Big) domains 7 and 8 (LigA7-8 and LigB7-8) of both LigA and LigB and also through LigB9-10. Therefore, C4BP and heparin may share the same binding sites on Lig proteins
Fine Mapping of the Interaction between C4b-Binding Protein and Outer Membrane Proteins LigA and LigB of Pathogenic Leptospira interrogans.
The complement system consists of more than 40 proteins that participate in the inflammatory response and in pathogen killing. Complement inhibitors are necessary to avoid the excessive consumption and activation of this system on host cells. Leptospirosis is a worldwide zoonosis caused by spirochetes from the genus Leptospira. Pathogenic leptospires are able to escape from complement activation by binding to host complement inhibitors Factor H [FH] and C4b-binding protein (C4BP) while non-pathogenic leptospires are rapidly killed in the presence of fresh serum. In this study, we demonstrate that complement control protein domains (CCP) 7 and 8 of C4BP α-chain interact with the outer membrane proteins LcpA, LigA and LigB from the pathogenic leptospire L. interrogans. The interaction between C4BP and LcpA, LigA and LigB is sensitive to ionic strength and inhibited by heparin. We fine mapped the LigA and LigB domains involved in its binding to C4BP and heparin and found that both interactions are mediated through the bacterial immunoglobulin-like (Big) domains 7 and 8 (LigA7-8 and LigB7-8) of both LigA and LigB and also through LigB9-10. Therefore, C4BP and heparin may share the same binding sites on Lig proteins
Relação entre os níveis de aflatoxina detectados em fígados e valores de AST e CK nos sorsos de frangos de corte
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Experimental study of negative photoconductivity in n-PbTe(Ga) epitaxial films
We report on low-temperature photoconductivity (PC) in n-PbTe(Ga) epitaxial
films prepared by the hot-wall technique on -BaF_2 substrates. Variation
of the substrate temperature allowed us to change the resistivity of the films
from 10^8 down to 10_{-2} Ohm x cm at 4.2 K. The resistivity reduction is
associated with a slight excess of Ga concentration, disturbing the Fermi level
pinning within the energy gap of n-PbTe(Ga). PC has been measured under
continuous and pulse illumination in the temperature range 4.2-300 K. For films
of low resistivity, the photoresponse is composed of negative and positive
parts. Recombination processes for both effects are characterized by
nonexponential kinetics depending on the illumination pulse duration and
intensity. Analysis of the PC transient proves that the negative
photoconductivity cannot be explained in terms of nonequilibrium charge
carriers spatial separation of due to band modulation. Experimental results are
interpreted assuming the mixed valence of Ga in lead telluride and the
formation of centers with a negative correlation energy. Specifics of the PC
process is determined by the energy levels attributed to donor Ga III, acceptor
Ga I, and neutral Ga II states with respect to the crystal surrounding. The
energy level corresponding to the metastable state Ga II is supposed to occur
above the conduction band bottom, providing fast recombination rates for the
negative PC. The superposition of negative and positive PC is considered to be
dependent on the ratio of the densities of states corresponding to the donor
and acceptor impurity centers.Comment: 7 pages, 4 figure
Effect of calcium salts of fatty acids on the nutritive value of diets, feeding behavior, and serum blood parameters of lactating Saanen goats grazing on stargrass
Aspectos morfológicos e de incubação em três espécies de Corbicula Mühlfeld, no lago Guaíba, Rio Grande do Sul, Brasil (Bivalvia, Corbiculidae)
Absence of Association between N-Acetyltransferase 2 Acetylator Status and Colorectal Cancer Susceptibility: Based on Evidence from 40 Studies
BACKGROUND AND OBJECTIVES: N-Acetyltransferase (NAT) 2 is an important enzyme involved in the metabolism of different xenobiotics, including potential carcinogens, whose phenotypes were reported to be related to individual susceptibility to colorectal cancer (CRC). However, the results remain conflicting. To assess the relationship between NAT2 phenotypes and CRC risk, we performed this meta-analysis. METHODS: A comprehensive literature search was conducted to identify all case-control or cohort studies of NAT2 acetylator status on the susceptibility of CRC by searching of PubMed and EMBASE, up to May 20, 2011. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the association. RESULTS: A total of over 40,000 subjects from 40 published literatures were identified by searching the databases. No significantly elevated CRC risk in individuals with NAT2 slow acetylators compared with fast acetylators was found when all studies pooled (OR = 0.95, 95% CI: 0.87-1.04, I(2) = 52.6%). While three studies contributed to the source of heterogeneity were removed, there was still null result observed (OR = 0.96, 95% CI: 0.90-1.03, P = 0.17 for heterogeneity, I(2) = 17.8%). In addition, we failed to detect any associations in the stratified analyses by race, sex, source of controls, smoking status, genotyping methods or tumor localization. No publication bias was observed in this study. CONCLUSIONS: This meta-analysis suggests that the NAT2 phenotypes may not be associated with colorectal cancer development
Reconstructing Native American Population History
The peopling of the Americas has been the subject of extensive genetic, archaeological and linguistic research; however, central questions remain unresolved1–5. One contentious issue is whether the settlement occurred via a single6–8 or multiple streams of migration from Siberia9–15. The pattern of dispersals within the Americas is also poorly understood. To address these questions at higher resolution than was previously possible, we assembled data from 52 Native American and 17 Siberian groups genotyped at 364,470 single nucleotide polymorphisms. We show that Native Americans descend from at least three streams of Asian gene flow. Most descend entirely from a single ancestral population that we call “First American”. However, speakers of Eskimo-Aleut languages from the Arctic inherit almost half their ancestry from a second stream of Asian gene flow, and the Na-Dene-speaking Chipewyan from Canada inherit roughly one-tenth of their ancestry from a third stream. We show that the initial peopling followed a southward expansion facilitated by the coast, with sequential population splits and little gene flow after divergence, especially in South America. A major exception is in Chibchan-speakers on both sides of the Panama Isthmus, who have ancestry from both North and South America
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