A specific method for measurement of equine active myeloperoxidase in biological samples and in in vitro testsFranck, Thierry ; Kohnen, Stephan ; et alin Journal of Veterinary Diagnostic Investigation (2006), 18(4), 326-334 An original method called SIEFED (specific immunological extraction followed by enzymatic detection) was developed for the specific detection of the activity of equine myeloperoxidase (MPO). The method ... [more ▼] An original method called SIEFED (specific immunological extraction followed by enzymatic detection) was developed for the specific detection of the activity of equine myeloperoxidase (MPO). The method consists of the extraction of MPO from aqueous solutions by immobilized anti-MPO antibodies followed by washing (to eliminate proteins and interfering molecules) and measurement of MPO activity using a detection system containing a fluorogenic substrate, hydrogen peroxide, and nitrite as reaction enhancer. The SIEFED technique was applied to study active MPO in horse biological fluids and the effects of 2 polyphenolic molecules, curcumin and resveratrol, on MPO activity. The detection limit of the SIEFED was 0.23 mU/ml. The SIEFED exhibited good precision with intra-assay and interassay coefficients of variation below 10% and 20%, respectively, for MPO activities ranging from 0.25 to 6.4 mU/ml. The activity of MPO was generally higher than 1 mU/ml in the fluids collected from horses with inflammatory diseases. Curcumin and resveratrol exerted a dose-dependent inhibition on MPO activity and, as they were removed before the enzymatic detection of MPO, the results suggest a direct drug-nzyme interaction or an enzyme structure modification by the drug. The SIEFED is a new tool that would be useful for specific detection of active MPO in complex media and for selection of MPO activity modulators. [less ▲] Detailed reference viewed: 38 (9 ULg) Specific Modulation Of The Fusogenic Properties Of The Alzheimer Beta-Amyloid Peptide By Apolipoprotein E Isoforms; ; et al in European Journal of Biochemistry (1997), 243(3), 650-9 C-terminal fragments of the Alzheimer amyloid peptide (amino acids 29-40 and 29-42) have physico-chemical properties related to those of the fusion peptides of viral proteins and they are able to induce ... [more ▼] C-terminal fragments of the Alzheimer amyloid peptide (amino acids 29-40 and 29-42) have physico-chemical properties related to those of the fusion peptides of viral proteins and they are able to induce the fusion of liposomes in vitro. We proposed that these properties could mediate a direct interaction of the amyloid peptide with cell membranes and account for part of the cytotoxicity of the amyloid peptide. In view of the epidemiologic and biochemical linkages between the pathology of Alzheimer's disease and apolipoprotein E (apoE) polymorphism, we examined the potential interaction between the three common apoE isoforms and the C-terminal fragments of the amyloid peptide. We show that, at low concentration, only apoE2 and apoE3 are potent inhibitors of the amyloid peptide fusogenic and aggregational properties, whereas the apoE4 isoform has no effect. We further show that the protective effect of apoE is mediated by the formation of stable apoE/amyloid peptide complexes, as determined by tryptophan emission fluorescence measurements and by gel electrophoresis. The interaction specificity between apoE2 and apoE3 and the amyloid fragments is demonstrated here, since other apolipoproteins (e.g. apolipoprotein A-I and A-II), with similar amphipathic structures, do not interact with the amyloid C-terminal fragments. Finally, we show that, reciprocally, the amyloid peptide can interact directly with the apoE2 and apoE3 isoforms to decrease or perturb their normal association with lipids. These data suggest that the 29-40 and 29-42 domains of the amyloid peptide could be critical for the amyloid-apoE interaction, and that apoE2 and apoE3 isoforms, but not apoE4, could play a protective role against the formation of amyloid aggregates and/or against their interaction with cellular membranes. [less ▲] Detailed reference viewed: 8 (3 ULg) Specific Passive Immunity Reduces the Excretion of Glycoprotein E-Negative Bovine Herpesvirus Type 1 Vaccine Strain in Calves; ; et al in Vaccine (2000), 19(9-10), 1013-7 We investigated the excretion of either a glycoprotein E (gE)-negative bovine herpesvirus type 1 (BHV1) vaccine strain or a conventional modified-live vaccine strain in both naive and passively immunised ... [more ▼] We investigated the excretion of either a glycoprotein E (gE)-negative bovine herpesvirus type 1 (BHV1) vaccine strain or a conventional modified-live vaccine strain in both naive and passively immunised calves. The replication of gE-negative strain was considerably reduced in the maternally immunised calves, in comparison with the non-immune calves. On the other hand, the excretion of the gE-positive conventional vaccine strain was not reduced and even seemed to be prolonged in the presence of maternal antibodies. These results suggest that BHV1 gE may play a role in virus survival in the presence of antibodies. [less ▲] Detailed reference viewed: 14 (0 ULg) A Specific Pcr to Differentiate between Ge Negative Vaccine and Wildtype Bovine Herpesvirus Type 1 Strains; ; et al in Veterinary Microbiology (1999), 66(3), 187-95 In the context of infectious bovine rhinotracheitis (IBR) control programmes using glycoprotein E (gE) deleted marker vaccines, a PCR assay was developed to allow the genotypic differentiation between ... [more ▼] In the context of infectious bovine rhinotracheitis (IBR) control programmes using glycoprotein E (gE) deleted marker vaccines, a PCR assay was developed to allow the genotypic differentiation between wildtype bovine herpesvirus type 1 (BoHV-1) and gE negative strains. This assay is based on the PCR amplification of a 281 bp DNA fragment within the gE gene. The specificity of the amplification was confirmed by restriction endonuclease analysis and nucleotide sequencing of the PCR product. Its ability to determine the gE genotype of BoHV-1 strains was demonstrated on isolates coming from 20 experimental calves infected with four different BoHV-1 strains. This PCR assay may be a useful tool for monitoring the spread of live marker vaccine and the gE genotype of viral field isolates. [less ▲] Detailed reference viewed: 6 (0 ULg) Specific phosphorylation of Torpedo 43 rapsyn by endogenous kinase(s) with thiamine triphosphate as the phosphate donor; Bettendorff, Lucien ; in FASEB Journal (2000), 14 Detailed reference viewed: 5 (3 ULg) Specific repertoire of olfactory receptor genes in the male germ cells of several mammalian species; Schurmans, Stéphane ; et alin Genomics (1997), 39 Olfactory receptors constitute the largest family among G protein-coupled receptors, with up to 1000 members expected. We have previously shown that genes belonging to this family were expressed in the ... [more ▼] Olfactory receptors constitute the largest family among G protein-coupled receptors, with up to 1000 members expected. We have previously shown that genes belonging to this family were expressed in the male germ line from both dog and human. We have subsequently demonstrated the presence of one of the corresponding olfactory receptor proteins during dog spermatogenesis and in mature sperm cells. In this study, we investigated whether the unexpected pattern of expression of olfactory receptors in the male germ line was conserved in other mammalian species. Using reverse transcription-PCR with primers specific for the olfactory receptor gene family, about 20 olfactory receptor cDNA fragments were cloned from the testis of each mammalian species tested. As a whole, they displayed no sequence specificity compared to other olfactory receptors, but highly homologous, possibly orthologous, genes were amplified from different species. Finally, their pattern of expression, as determined by RNase protection assay, revealed that many but not all of these receptors were expressed predominantly in testis. The male germ line from each mammalian species tested ins thus characterized by a specific repertoire of olfactory receptors, which display a pattern of expression suggestive of their potential implication in the control of sperm maturation, migration, or fertilization [less ▲] Detailed reference viewed: 30 (2 ULg) Specific risks of anesthesia in patients with osteoarticular diseaseReginster, Jean-Yves ; Damas, Pierre ; in Acta Anaesthesiologica Belgica (1984), 35(2), 105-121 Anesthesia in patients with either treated or untreated osteoarttcular disorders poses a number of specific problems. The authors deal with risks resulting from mechanical deformities produced by these ... [more ▼] Anesthesia in patients with either treated or untreated osteoarttcular disorders poses a number of specific problems. The authors deal with risks resulting from mechanical deformities produced by these disorders, by the involvement of a large number of functional systems, by changes in the immune status of such patients and by alterations in the reactions of arthritic patients resulting from prior or concurrent treatments. The authors emphasise the crucial points which require evaluation and observation before and during anesthesia [less ▲] Detailed reference viewed: 8 (1 ULg) A specific role for spermidine in the initiation phase of somatic embryogenesis in Panax ginseng CA Meyer; Kevers, Claire ; Dommes, Jacques et alin Plant Cell, Tissue & Organ Culture (2002), 68(3), 225-232 Somatic embryogenesis of Panax ginseng CA Meyer was initiated from suspension aggregates of an embryogenic callus, in a liquid medium consisting of half strength Murashige and Skoog (1962) supplemented ... [more ▼] Somatic embryogenesis of Panax ginseng CA Meyer was initiated from suspension aggregates of an embryogenic callus, in a liquid medium consisting of half strength Murashige and Skoog (1962) supplemented with the synthetic auxin benzoselenienyl-3 acetic acid. The addition of spermidine to this initiation medium significantly increased the production of somatic embryos. In this case, the total polyamine content of the embryogenic mass was higher than that of cultures without spermidine. At day 6 of the culture, a transient accumulation of free polyamines, mainly spermidine, was observed. After this peak, free and conjugated polyamines levels did not show significant variation nor did the polyamine oxidase activity. The results clearly demonstrated that spermidine supplied to the medium was oxidised by polyamine oxidase and partially metabolised into putrescine. The role of spermidine and its interaction with auxin in the initiation of the embryogenic process in Panax ginseng are discussed in relation to embryogenic potential. [less ▲] Detailed reference viewed: 32 (2 ULg) Specific Structural Features of the N-Acetylmuramoyl-l-Alanine Amidase AmiD from Escherichia coli and Mechanistic Implications for Enzymes of This Family.Kerff, Frédéric ; ; Mercier, Frédéric et alin Journal of Molecular Biology (2010), 397 AmiD is the fifth identified N-acetylmuramoyl-l-alanine zinc amidase of Escherichia coli. This periplasmic lipoprotein is anchored in the outer membrane and has a broad specificity. AmiD is capable of ... [more ▼] AmiD is the fifth identified N-acetylmuramoyl-l-alanine zinc amidase of Escherichia coli. This periplasmic lipoprotein is anchored in the outer membrane and has a broad specificity. AmiD is capable of cleaving the intact peptidoglycan (PG) as well as soluble fragments containing N-acetylmuramic acid regardless of the presence of an anhydro form or not, unlike the four other amidases, AmiA, AmiB, AmiC, and AmpD, which have some specificity. AmiD function is, however, not clearly established but it could be part of the enzymatic machinery involved in the PG turnover in E. coli. We solved three structures of the E. coli zinc amidase AmiD devoid of its lipidic anchorage: the holoenzyme, the apoenzyme in complex with the substrate anhydro-N-acetylmuramic-acid-l-Ala-gamma-d-Glu-l-Lys, and the holoenzyme in complex with the l-Ala-gamma-d-Glu-l-Lys peptide, the product of the hydrolysis of this substrate by AmiD. The AmiD structure shows a relatively flexible N-terminal extension that allows an easy reach of the PG by the enzyme inserted into the outer membrane. The C-terminal domain provides a potential extended geometrical complementarity to the substrate. AmiD shares a common fold with AmpD, the bacteriophage T7 lysozyme, and the PG recognition proteins, which are receptor proteins involved in the innate immune responses of a wide range of organisms. Analysis of the different structures reveals the similarity between the catalytic mechanism of zinc amidases of the AmiD family and the thermolysin-related zinc peptidases. [less ▲] Detailed reference viewed: 73 (16 ULg) Specific structural features of the N-acetylmuramyl-L-Alanine amidase AmiD from E.coli and general implication for the mechanism of action of this family of enzymeKerff, Frédéric ![]() Poster (2008, August) Detailed reference viewed: 4 (0 ULg) Specific topics on Bénard-Marangoni instabilitiesDesaive, Thomas ; Dauby, Pierre ; Lebon, Georgy et alin Henry, Daniel; Bergeon, Alain (Eds.) Proceedings of the ERCOFTAC and EUROMECH Colloquium 383 on Continuation Methods in Fluid Dynamics (2000) Detailed reference viewed: 16 (6 ULg) Specific transcription factors control the c-erbB2 gene expression in the mammary tumor BT-474 cells.; Pasleau, Françoise ; et alConference (1995, December) Detailed reference viewed: 17 (1 ULg) Specific transcription factors of the tumor BT-474 mammary cells regulate the c-erbB2 gene expression.; Pasleau, Françoise ; Conference (1994, December 22) Detailed reference viewed: 7 (0 ULg) Specific transcription factors of the tumor BT-474 mammary cells.; Pasleau, Françoise ; Conference (1995, January 21) Detailed reference viewed: 7 (0 ULg) Specific transcription factors regulate the c-erbB2 expression in the tumor BT-474 mammary cells.; Pasleau, Françoise ; Conference (1995, March 24) Detailed reference viewed: 3 (0 ULg) Specific uptake of N-isopropyl-p-I-123-iodomphetamine by the adrenal cortex.; Beckers, Albert ; et alin Nuclear Medicine Communications (1987) Detailed reference viewed: 3 (1 ULg) Specification and verification of a TTP protocol for the conditional access to servicesLeduc, Guy ; ; et alin Formal Methods and their Applications: Telecommunications, VLSI and Real-Time Computerized Control Systems (1996, October) We use the formal language LOTOS to specify the Equicrypt protocol and verify its robustness to attacks by an intruder. We use the model-based CADP verification tools from the Eucalyptus toolbox to ... [more ▼] We use the formal language LOTOS to specify the Equicrypt protocol and verify its robustness to attacks by an intruder. We use the model-based CADP verification tools from the Eucalyptus toolbox to discover some successful attacks against this protocol. [less ▲] Detailed reference viewed: 37 (2 ULg) Spécification formelle des mécanismes de support des qualités de service dans l'InternetLeduc, Guy ; in Ingénierie des protocoles et qualité de service (2001) Detailed reference viewed: 19 (3 ULg) Spécification géométrique des concepts architecturaux dans le cadre de la thermique du bâtimentJuchmes, Roland ; Delfosse, Vincent ; Safin, Stéphane et alin Tidafi, T.; Dorta, T. (Eds.) Joindre langages, cultures & visions (2009) Cette étude s’intéresse à l’assignation des propriétés technologiques des parois dans un modeleur architectural 3D. Nous proposons une méthode originale basée sur le principe de groupements sémantiques de ... [more ▼] Cette étude s’intéresse à l’assignation des propriétés technologiques des parois dans un modeleur architectural 3D. Nous proposons une méthode originale basée sur le principe de groupements sémantiques de faces par requêtes géométriques. Nous décrivons la méthode et les résultats d’entretiens menés auprès d’architectes pour identifier les groupements pertinents, listons les requêtes géométriques simples pour la sélection de ces groupements et rendons compte de l’efficacité de la méthode sur un cas. Nous concluons sur les avantages et limites de l’approche. [less ▲] Detailed reference viewed: 87 (10 ULg) Specification of an extensible and portable file format for electronic structure and crystallographic data; ; et al in Computational Materials Science (2008), 43 Detailed reference viewed: 10 (4 ULg) |
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