Relevant bibliographies by topics / LPS- binding proteins

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'LPS- binding proteins'

Author: Grafiati
Published: 9 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "LPS- binding proteins"

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Fenton, Matthew J., and Douglas T. Golenbock. "LPS-binding proteins and receptors." Journal of Leukocyte Biology 64, no. 1 (1998): 25–32. http://dx.doi.org/10.1002/jlb.64.1.25.

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Hailman, E., H. S. Lichenstein, M. M. Wurfel, et al. "Lipopolysaccharide (LPS)-binding protein accelerates the binding of LPS to CD14." Journal of Experimental Medicine 179, no. 1 (1994): 269–77. http://dx.doi.org/10.1084/jem.179.1.269.

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CD14 is a 55-kD protein found as a glycosylphosphatidylinositol (GPI)-anchored protein on the surface of monocytes, macrophages, and polymorphonuclear leukocytes, and as a soluble protein in the blood. Both forms of CD14 participate in the serum-dependent responses of cells to bacterial lipopolysaccharide (LPS). While CD14 has been described as a receptor for complexes of LPS with LPS-binding protein (LBP), there has been no direct evidence showing whether a ternary complex of LPS, LBP, and CD14 is formed, or whether CD14 binds LPS directly. Using nondenaturing polyacrylamide gel electrophores
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Schumann, R. R., N. Lamping, and A. Hoess. "Interchangeable endotoxin-binding domains in proteins with opposite lipopolysaccharide-dependent activities." Journal of Immunology 159, no. 11 (1997): 5599–605. http://dx.doi.org/10.4049/jimmunol.159.11.5599.

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Abstract Host defense against microorganisms involves proteins that bind specifically to bacterial endotoxins (LPS), causing different cellular effects. Although LPS-binding protein (LBP) can enhance LPS activities, while bactericidal/permeability-increasing protein (BPI) and Limulus anti-LPS factor (LALF) neutralize LPS, it has been proposed that their LPS-binding domains possess a similar structure. Here, we provide evidence that the LBP/LPS-binding domain is, as in the LALF structure, solvent exposed and therefore available for LPS binding. Our investigations into the activity of LPS-bindin
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Qureshi, N., P. Y. Perera, J. Shen, et al. "NOVEL LPS-BINDING PROTEINS IN MURINE MACROPHAGES." Shock 17, Supplement (2002): 28. http://dx.doi.org/10.1097/00024382-200206001-00082.

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Lei, M. G., and D. C. Morrison. "Specific endotoxic lipopolysaccharide-binding proteins on murine splenocytes. II. Membrane localization and binding characteristics." Journal of Immunology 141, no. 3 (1988): 1006–11. http://dx.doi.org/10.4049/jimmunol.141.3.1006.

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Abstract We have characterized the binding of LPS to an 80-kDa LPS-binding protein detected by an LPS photoaffinity probe to be present on murine splenocytes. Specific binding of LPS to the 80-kDa protein is directly proportional to LPS concentration at low concentrations of LPS and is saturable at high concentrations of LPS. Binding is inhibited by both homologous and heterologous underivatized LPS as well as by polysaccharide-free lipid A, indicating a specificity for the biologically active component of LPS. Analysis of the kinetics of binding indicate a time-dependent increase over the fir
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Naberezhnykh, G., V. Davydova, and T. Soloveva. "INTERACTION OF LIPOPOLYSACCHARIDE-BINDING PROTEINS WITH VARIOUS FORMS OF LIPOPOLYSACCHARIDES." Russian Journal of Biological Physics and Chemisrty 8, no. 2 (2024): 178–84. http://dx.doi.org/10.29039/rusjbpc.2023.0606.

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Lipopolysaccharide-binding proteins from two common jellyfish species Aurellia aurita and Ropelema asamushi were isolated and purified, and the interaction of lipopolysaccharides (LPS) of various structural types with LBP was studied. By inhibiting the interaction, it was found that both proteins specifically bind to the lipid and core fragments of the LPS molecule. There are two types of binding sites in LBP with Kd = 3,28 × 10-6 M and Kd = 0,13 × 10-6 M (for the protein from A. aurita) and Kd = 3,66 × 10-6 M and Kd = 0,27 × 10-6 M (for protein from R. asamushi). It has been shown by dynamic
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Elass-Rochard, Elisabeth, Dominique Legrand, Valerie Salmon, et al. "Lactoferrin Inhibits the Endotoxin Interaction with CD14 by Competition with the Lipopolysaccharide-Binding Protein." Infection and Immunity 66, no. 2 (1998): 486–91. http://dx.doi.org/10.1128/iai.66.2.486-491.1998.

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ABSTRACT Human lactoferrin (hLf), a glycoprotein released from neutrophil granules during inflammation, and the lipopolysaccharide (LPS)-binding protein (LBP), an acute-phase serum protein, are known to bind to the lipid A of LPS. The LPS-binding sites are located in the N-terminal regions of both proteins, at amino acid residues 28 to 34 of hLf and 91 to 108 of LBP. Both of these proteins modulate endotoxin activities, but they possess biologically antagonistic properties. In this study, we have investigated the competition between hLf and recombinant human LBP (rhLBP) for the binding of Esch
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Weersink, A. J., K. P. van Kessel, M. E. van den Tol, et al. "Human granulocytes express a 55-kDa lipopolysaccharide-binding protein on the cell surface that is identical to the bactericidal/permeability-increasing protein." Journal of Immunology 150, no. 1 (1993): 253–63. http://dx.doi.org/10.4049/jimmunol.150.1.253.

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Abstract Several LPS-binding proteins have been identified on the surface of human granulocytes (polymorphonuclear leukocyte (PMN)). We describe a plasma-membrane associated ca. 55-kDa LPS-binding protein of human PMN that is indistinguishable from the bactericidal/permeability-increasing protein (BPI). To detect LPS-binding proteins on the cell surface, PMN were biotinylated before detergent solubilization and incubation with LPS-coated beads. Several biotinylated proteins bound to LPS-coated beads but not to uncoated beads and were characterized after elution with detergent by SDS-PAGE and w
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Tobias, P. S., K. Soldau, L. Kline, et al. "Cross-linking of lipopolysaccharide (LPS) to CD14 on THP-1 cells mediated by LPS-binding protein." Journal of Immunology 150, no. 7 (1993): 3011–21. http://dx.doi.org/10.4049/jimmunol.150.7.3011.

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Abstract Recent work has established that bacterial endotoxin (LPS) binds to the plasma protein LPS-binding protein (LBP) forming high affinity complexes (LPS-LBP), that LBP is an opsonin for LPS-bearing particles, and that LPS-LBP complexes are potent agonists for monocytic cells (MO). mAb to the MO plasma membrane protein, CD14, inhibit LBP-dependent binding of LPS to MO, and LPS-LBP-dependent stimulation of cytokine release from MO. These data suggest that CD14 functions as a membrane receptor for LPS but do not demonstrate a direct association of LPS with CD14. Calcitriol was used to induc
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Amura, Claudia R., Takayuki Kamei, Noriko Ito, Michael J. Soares, and David C. Morrison. "Differential Regulation of Lipopolysaccharide (LPS) Activation Pathways in Mouse Macrophages by LPS-Binding Proteins." Journal of Immunology 161, no. 5 (1998): 2552–60. http://dx.doi.org/10.4049/jimmunol.161.5.2552.

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Abstract LPS binding to its receptor(s) on macrophages induces the synthesis of inflammatory mediators involved in septic shock. While the signaling mechanism(s) remains to be fully defined, the human LPS-binding protein (LBP) is known to regulate responses to LPS by facilitating its binding to CD14 on human monocytes. The structurally related bactericidal permeability increasing protein (BPI) differs from LBP by inhibiting LPS-induced human monocyte activation. We have demonstrated that, unlike the human monocyte response to LPS, both LBP and BPI inhibited LPS-stimulated TNF-α production in m
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Dissertations / Theses on the topic "LPS- binding proteins"

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SESTITO, STEFANIA ENZA. "LPS-binding proteins: interaction studies with natural and synthetic ligands." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2015. http://hdl.handle.net/10281/67756.

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L’obiettivo di questa tesi è elucidare alcuni aspetti dell’interazione tra proteine che legano il lipopolisaccaride (LPS) batterico e il loro ligando naturale o ligandi di sintesi. LptC (Lipopolysaccharide transport C) è una proteina batterica che appartiene al sistema di trasporto Lpt, un sistema di 7 proteine essenziali che trasportano l’LPS sulla membrana esterna dei batteri Gram negativi dopo la sua biosintesi. Sebbene molti elementi della biosintesi dell’LPS siano stati elucidati, il preciso meccanismo di trasporto è ancora poco chiaro. Poiché LptC può essere considerata come proteina m
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CIARAMELLI, CARLOTTA. "Synthesis and characterization of new small-molecule ligands of LPS binding proteins." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2015. http://hdl.handle.net/10281/77016.

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Lo scopo del presente lavoro è la progettazione, la sintesi e la caratterizzazione di nuove small molecules, attive come ligandi di LPS (lipopolisaccaridi)-binding proteins. Gli LPS, o endotossine batteriche, sono macromolecole anfifiliche ubiquitarie sulla membrana esterna dei batteri Gram-negativi. Le proteine che legano gli LPS studiate nel corso di questo progetto di tesi di dottorato appartengono a due categorie: le proteine batteriche di trasporto Lpt e il sistema recettoriale TLR4, che comprende anche i co-recettori LBP, CD14, MD2. Le proteine Lpt, e in particolare la proteina LptC, so
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Eckert, Jana Kristin. "Funktionelle Analyse von Mutanten des LPS-bindenden Proteins (LBP)." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2009. http://dx.doi.org/10.18452/15955.

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LBP vermittelt im Wirtsorganismus die direkte Immunantwort auf bakterielle Liganden wie das Lipopolysaccharid (LPS) von Gram-negativen oder Lipopeptide von Gram-positiven Bakterien. In dieser Arbeit wurde die Funktionsweise von LBP weiter aufgeklärt. Im ersten Teil der Arbeit wurde eine natürlich vorkommende Mutation des LBP (c998t), die an Position 333 zu einem Austausch der Aminosäure Prolin zu Leucin führt, hinsichtlich ihrer Auswirkungen auf Struktur und Funktionalität des Proteins untersucht. Westernblot-Analysen des rekombinant hergestellten Proteins und humaner Seren von Mutationsträger
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Szpryngiel, Scarlett. "Structure and lipid interactions of membrane-associated glycosyltransferases : Cationic patches and anionic lipids regulate biomembrane binding of both GT-A and GT-B enzymes." Doctoral thesis, Stockholms universitet, Institutionen för biokemi och biofysik, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-131084.

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This thesis concerns work on structure and membrane interactions of enzymes involved in lipid synthesis, biomembrane and cell wall regulation and cell defense processes. These proteins, known as glycosyltransferases (GTs), are involved in the transfer of sugar moieties from nucleotide sugars to lipids or chitin polymers. Glycosyltransferases from three types of organisms have been investigated; one is responsible for vital lipid synthesis in Arabidopsis thaliana (atDGD2) and adjusts the lipid content in biomembranes if the plant experiences stressful growth conditions. This enzyme shares many
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Hallatschek, Werner. "Die Regulation des humanen Lipopolysaccharid bindenden Proteins (hLBP)." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2005. http://dx.doi.org/10.18452/15202.

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Das Lipopolysaccharid Bindende Protein (LBP) ist ein überwiegend in der Leber synthetisiertes Akutphaseprotein. Es bindet den Zellwandbestandteil Lipopolysaccharid (LPS) Gram-negativer Bakterien und transportiert es zu zellulären Rezeptoren, wodurch das angeborene Immunsystem aktiviert wird. In dieser Arbeit wird die Regulation der LBP-Expression in Interleukin (IL)-1, IL-6 und Dexamethason (Dex) stimulierten humanen Hepatomzelllinien HuH-7 und HepG2 untersucht. Der wichtigste Stimulator ist dabei IL-6, dessen Wirkung über die Transkriptionsfaktoren (TF) Stat-3, C/EBP-beta und AP-1 vermittel
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ZAFFARONI, LENNY. "Production of recombinant human MD-2 and development of protein-ligand binding assays for the characterization of new TLR4 modulators." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2018. http://hdl.handle.net/10281/207343.

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Il toll-like receptor 4 (TLR4) rappresenta un mediatore centrale dell’immunità innata ed adattativa in mammiferi. L’attivazione di TLR4 in risposta al lipopolisaccaride (LPS) batterico induce un rapido innesco di processi pro-infiammatori essenziali per una risposta immunitaria ottimale. L’attivazione di TLR4 mediata da LPS è un meccanismo che coinvolge la partecipazione di diverse proteine e culmina con la formazione del complesso attivato (TLR4/MD-2/LPS)2. MD-2 è il co-rettore di TLR4, e svolge un importante ruolo nell’interazione con LPS e la susseguente dimerizzazione del TLR4. MD-2 è la c
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Ghanim, Mustafa. "Les aspects génétiques des démences frontotemporales." Paris 6, 2010. http://www.theses.fr/2010PA066039.

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Agostini, Federico 1985. "Predictions of RNA-binding ability and aggregation propensity of proteins." Doctoral thesis, Universitat Pompeu Fabra, 2014. http://hdl.handle.net/10803/318159.

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RNA-binding proteins (RBPs) control the fate of a multitude of coding and non-coding transcripts. Formation of ribonucleoprotein (RNP) complexes fine-tunes regulation of post-transcriptional events and influences gene expression. Recently, it has been observed that non-canonical proteins with RNA-binding ability are enriched in structurally disordered and low-complexity regions that are generally involved in functional and dysfunctional associations. Therefore, it is possible that interactions with RNA protect unstructured protein domains from aberrant associations or aggregation. Nevertheless
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Ding, Peihui, and 丁佩惠. "Expression profile, molecular regulation and immuno-inflammatory function of LPS-binding protein in human oral keratinocytes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B49617795.

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Lipopolysaccharide (LPS)-binding protein (LBP) functions as a crucial molecule in innate immune responses to bacterial challenge. Our recent study shows the expression of LBP in human gingiva and its significant association with periodontal condition. Porphyromonas gingivalis is a keystone periodontopathogen with its LPS as a major virulence factor strongly involved in periodontal pathogenesis. Recent study has discovered that P. gingivalis LPS displays a significant lipid A structural heterogeneity. The present study investigated i) the expression profile of LBP in human oral keratinocytes (
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Gonzalez, Daniel. "Les "phosphate binding protein" : entre import du phosphate et inhibition de la transcription virale." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4019.

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Les « phosphate binding protein » (PBP) constituent une famille de protéines présentes de manière ubiquitaire chez les bactéries et plus marginalement chez les Eucaryotes. Impliquées dans l'import du phosphate extracellulaire chez les bactéries, les PBPs présentent un site de fixation du phosphate très bien caractérisé avec, notamment, une liaison hydrogène particulière nommée «low barrier hydrogen bond» (LBHB). Cette LBHB est impliquée dans la discrimination entre le phosphate et des anions proches chez les PBPs. Bien que cette discrimination semble nécessiter une haute conservation du site d
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Books on the topic "LPS- binding proteins"

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Wiklund, Olov, and Jan Borén. Pathogenesis of atherosclerosis: lipid metabolism. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755777.003.0011.

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Lipids are carried in plasma as microparticles, lipoproteins, composed of a core of hydrophobic lipids and a surface of amphipathic lipids. In addition, the particles carry proteins (i.e. apolipoproteins). The proteins have key functions in the metabolism as receptor ligands, enzymes or activators. Lipoproteins are classified based on density into: chylomicrons, VLDL, IDL, LDL, and HDL. Retention of apoB-containing lipoproteins (LDL, IDL, and VLDL) in the arterial intima is the initiating event in the development of atherosclerosis. Retention is mediated by binding of apoB to structural proteo
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Book chapters on the topic "LPS- binding proteins"

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Ohno, Naohito. "LPS Binding Proteins in Granulocyte Lysosomes." In Bacterial Endotoxic Lipopolysaccharides. CRC Press, 2024. https://doi.org/10.1201/9781003574859-19.

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Hirata, M., M. Yoshida, K. Inada, and T. Kirikae. "Investigation of Endotoxin Binding Cationic Proteins from Granulocytes; Agglutination of Erythrocytes Sensitized with Re-LPS." In Endotoxin. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-5140-6_25.

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Lefèvre, G. "Le h-FABP (Heart Fatty Acid Binding Protein)." In Les biomarqueurs en médecine d’urgence. Springer Paris, 2012. http://dx.doi.org/10.1007/978-2-8178-0297-8_16.

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Taylor, A. H., M. Nedelman, D. Sherris, et al. "Structure-function analysis of LPS neutralizing synthetic peptides derived from human LPS binding protein." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_298.

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Zemene, Abebe. "The Employment of Polymerase Chain Reaction in Building Phage Displayed Antibody Libraries." In Polymerase Chain Reaction Research. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.110729.

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“The power of evolution is revealed through the diversity of life,” says the announcement for the 2018 Nobel Prize in chemistry, George Smith described phage display technology in 1985, and it has since been expanded to include the display of peptides, various recombinant antibody formats, enzymes, and fragmented proteomes. These phage libraries can display a wide range of ligands on coat proteins projecting from the surface of the bacteriophage particle, with the ligand-coat protein fusion encoded using either a phagemid or phage vector system. Most phages have a high affinity for host cell s
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BELAN, P., V. CHERKAS, O. MARKOVA, D. FITZGERALD, A. TEPIKIN, and R. D. BURGOYNE. "SPONTANEOUS HIPPOCALCIN TRANSLOCATION IN HIPPOCAMPAL NEURONS." In ESSAYS ON NEUROPHYSIOLOGY BY PLATON KOSTYUK AND HIS STUDENTS. AKADEMPERIODYKA, 2020. https://doi.org/10.15407/biph.books.essneur.299.

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Hippocalcin is a Ca2+-binding protein, which belongs to the family of neuronal Cahe brain have not been investigated in detail. the brain have not been investigated in detail. Th e molecular mechanism, by which hippocalcin operates, is thought to be a Ca2+/myristoyl switch (Burgoyne, 2007). Hippocalcin is N-terminally myristoylated and myristoyl group is sequestered in the Ca2+ free form of the protein and following Ca2+-binding a substantial conformational change allows extrusion of the lipophilic myristoyl group (Ames et al., 1997) resulting in the protein translocation from cytosol to membr
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Jaiswal, Anju, Asha Kumari, and Rashmi Singh. "Role of NLRP3 Inflammasome in Airway Inflammation and Fibrosis." In The NLRP3 Inflammasome: An Attentive Arbiter of Inflammatory Response. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223941124010003.

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The NLRP3 inflammasome is a critical component of the innate immune system that mediates caspase-1 activation and the secretion of proinflammatory cytokines IL-1β/IL-18 in response to microbial infection and cellular damage. Nucleotide-binding oligomerization domain (NOD)-like receptor family pyrin domain 3 (NLRP3), one of the members of the NLR family, consists of NLRP3, the adaptor molecule, apoptosis-associated speck-like protein containing a caspase and recruitment domain (ASC) and an inflammatory caspase-1 that causes excessive inflammasome activation in respiratory diseases like asthma a
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Janero, David R., Anisha Korde, and Alexandros Makriyannis. "Ligand-Assisted Protein Structure (LAPS): An Experimental Paradigm for Characterizing Cannabinoid-Receptor Ligand-Binding Domains." In Methods in Enzymology. Elsevier, 2017. http://dx.doi.org/10.1016/bs.mie.2017.06.022.

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Conference papers on the topic "LPS- binding proteins"

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Tokunaga, F., T. Miyata, T. Nakamura, T. Morita, and S. Iwanaga. "LIPOPOLYSACCHARIDE-SENSITIVE SERINE-PROTEASE ZYMOGEN (FACTOR C) OF LIMULUS HEMOCYTES: IDENTIFICATION AND ALIGNMENT OF PROTEOLYTIC FRAGMENTS PRODUCED DURING THE ACTIVATION SHOW THAT IT IS A NOVEL TYPE OF SERINE-PROTEASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644609.

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Limulus clotting factor, factor C, is a lipopolysaccharide (LPS)-sensitive serine-protease zymogen present in the hemocytes. It is a two-chain glycoprotein (M.W. = 123,000) composed of a heavy chain (M.W. = 80,000) and a light chain (M.W. = 43,000) T. Nakamura et al. (1986) Eur. J. Biochem. 154, 511-521 .On further studies of this zymogen, a single-chain factor C (M.W. = 123,000) was identified by Western blotting technique. The heavy chain had an NH2-terminal sequence of Ser-Gly-Val-Asp-, which was consistent with the NH2-terminal sequence of the single-chain factor C, indicating that the hea
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Steiner, Robert F., and Lynn Norris. "Fluorescence Dynamics Of Calcium-Binding Proteins." In OE LASE'87 and EO Imaging Symp (January 1987, Los Angeles), edited by E. R. Menzel. SPIE, 1987. http://dx.doi.org/10.1117/12.966939.

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Morozkina, Svetlana N., Petr P. Snetkov, and Mayya V. Uspenskaya. "Docking of Small Molecules with in Vivo Cardiovascular Activity into The Proteins – The Relationship with Side-Effects." In International Medicine and Health Sciences Congress. ECER, 2024. https://doi.org/10.53375/imhsc.2024.35.

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Cardiac amyloidosis is a clinical pathology, usually of a genetically mediated nature, initiated by the formation of amyloid fibrils, that lead to death. The number of clinically used molecules for the treatment of cardiac amyloidosis is very limited with strong side effects (for example, tafamidis and diflunisal). In this study, the methods of molecular modeling and computer docking of ligands using ICM-pro (Molsoft LLS, USA) were used to evaluate for the first time the level of side binding of small molecules possessing in vivo cardiovascular activity into the ligand-binding domains of 136 p
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Ye, Xiaobing, and Shu F. Liu. "LPS Differentially Regulates Specificity Protein (Sp1) DNA Binding Activity In Heart, Lungs And Liver." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a4951.

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Lan, Jianqing, and Robert F. Steiner. "Studies of the interactions between calcium-binding proteins and phosphofructokinase using fluorescent probes." In OE/LASE '90, 14-19 Jan., Los Angeles, CA, edited by Joseph R. Lakowicz. SPIE, 1990. http://dx.doi.org/10.1117/12.17749.

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Mao, Sun-Zhong, Xiaobing Ye, and Shu F. Liu. "LPS Down-Regulates Specificity Protein 1 DNA Binding Activity Through Nf-&kB Signaling Pathway In Endotoxemic Mice." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5772.

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Bein, Kiflai, and George Leikauf. "Macrophages Mediate LPS-Induced Increased CCAAT/enhancer Binding Protein (C/EBP), Beta (C/EBP-Beta) Transcripts In Lung Epithelial Cells." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5099.

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Pannekok, H., A. J. Van Zonneveid, C. J. M. de vries, M. E. MacDonald, H. Veerman, and F. Blasi. "FUNCTIONAL PROPERTIES OF DELETION-MUTANTS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643724.

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Over the past twenty-five years, genetic methods have generated a wealth of information on the regulation and the structure-function relationship of bacterial genes.These methods are based on the introduction of random mutations in a gene to alter its function. Subsequently, genetic techniques cure applied to localize the mutation, while the nature of the impairedfunction could be determined using biochemical methods. Classic examples of this approach is now considered to be the elucidation of the structure and function of genes, constituting the Escherichia coli lactose (lac) and tryptophan (
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