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Relevant bibliographies by topics / Endoglycosidase

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Academic literature on the topic 'Endoglycosidase'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 January 2023

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Journal articles on the topic "Endoglycosidase"

1

Gallagher, J. T., A. Walker, M. Lyon, and W. H. Evans. "Heparan sulphate-degrading endoglycosidase in liver plasma membranes." Biochemical Journal 250, no. 3 (1988): 719–26. http://dx.doi.org/10.1042/bj2500719.

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An endoglycosidase is described in isolated liver plasma membranes that brings about a rapid and selective degradation of membrane-associated heparan sulphate, pre-labelled biosynthetically with Na2(35)SO4. The enzyme attacked mainly the polysaccharide chains of a hydrophobic membrane proteoglycan and it had little effect on a proteoglycan that could be displaced from the membranes with 1.0 M-NaCl. The highest activity was measured in the pH range 7.5-8.0, and the enzyme was almost completely inhibited below pH 5.5. Breakdown of susceptible polysaccharide chains was fast, being complete in 20-

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2

Majumder, S., K. Brown, F. H. Qiu, and P. Besmer. "c-kit protein, a transmembrane kinase: identification in tissues and characterization." Molecular and Cellular Biology 8, no. 11 (1988): 4896–903. http://dx.doi.org/10.1128/mcb.8.11.4896-4903.1988.

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The proto-oncogene c-kit encodes a transmembrane kinase which is related to the receptors for colony-stimulating factor type 1 and platelet-derived growth factor, as well as to the immunoglobulin superfamily. Antibodies specific for the kinase domain of the P80 gag-kit protein of the Hardy-Zuckerman 4 feline sarcoma virus were prepared. These kit-specific antibodies were used to identify and characterize the c-kit protein in cat brain tissue. The c-kit protein product displays an autophosphorylating activity in immune complex kinase assays, and, in turn, this activity was used to identify the

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Majumder, S., K. Brown, F. H. Qiu, and P. Besmer. "c-kit protein, a transmembrane kinase: identification in tissues and characterization." Molecular and Cellular Biology 8, no. 11 (1988): 4896–903. http://dx.doi.org/10.1128/mcb.8.11.4896.

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The proto-oncogene c-kit encodes a transmembrane kinase which is related to the receptors for colony-stimulating factor type 1 and platelet-derived growth factor, as well as to the immunoglobulin superfamily. Antibodies specific for the kinase domain of the P80 gag-kit protein of the Hardy-Zuckerman 4 feline sarcoma virus were prepared. These kit-specific antibodies were used to identify and characterize the c-kit protein in cat brain tissue. The c-kit protein product displays an autophosphorylating activity in immune complex kinase assays, and, in turn, this activity was used to identify the

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4

Swedlow, J. R., R. L. Matteri, and H. Papkoff. "Deglycosylation of Gonadotropins with an Endoglycosidase." Experimental Biology and Medicine 181, no. 3 (1986): 432–37. http://dx.doi.org/10.3181/00379727-181-42277.

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5

Paton, B. C., and A. Poulos. "Analysis of the multiple forms of Gaucher spleen sphingolipid activator protein 2." Biochemical Journal 254, no. 1 (1988): 77–84. http://dx.doi.org/10.1042/bj2540077.

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Gaucher spleen sphingolipid activator protein 2 was fractionated into concanavalin A binding- and non-binding fractions. These fractions each contained several bands on non-denaturing polyacrylamide gel electrophoresis (PAGE). The two fractions were further fractionated by electroblotting the proteins from preparative gels onto nitrocellulose, staining with Ponceau S to locate the bands of protein and then eluting the protein components from the nitrocellulose. A total of ten fractions, each containing only one or two major components, was collected. All of these subfractions activated beta-gl

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Lublin, D. M., J. Krsek-Staples, M. K. Pangburn, and J. P. Atkinson. "Biosynthesis and glycosylation of the human complement regulatory protein decay-accelerating factor." Journal of Immunology 137, no. 5 (1986): 1629–35. http://dx.doi.org/10.4049/jimmunol.137.5.1629.

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Abstract The biosynthesis and oligosaccharide structure of the human complement regulatory glycoprotein decay-accelerating factor (DAF) were studied in erythrocytes and cell lines. Initial information relative to carbohydrate moieties of DAF was obtained by enzymatic digestions. The 74,000 Mr erythrocyte DAF was lowered 3000 by endoglycosidase F, whereas endoglycosidase H had no effect, indicating one N-linked complex-type unit. Treatment with endo-alpha-N-acetylgalactosaminidase to remove O-linked oligosaccharides resulted in a 48,000 Mr molecule (67% of the Mr shift being due to sialic acid)

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Torok, Rebeka, Felicia Auer, Robert Farsang, Eszter Jona, Gabor Jarvas, and Andras Guttman. "The Effect of Sample Glucose Content on PNGase F-Mediated N-Glycan Release Analyzed by Capillary Electrophoresis." Molecules 27, no. 23 (2022): 8192. http://dx.doi.org/10.3390/molecules27238192.

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Protein therapeutics have recently gained high importance in general health care along with applied clinical research. Therefore, it is important to understand the structure–function relationship of these new generation drugs. Asparagine-bound carbohydrates represent an important critical quality attribute of therapeutic glycoproteins, reportedly impacting the efficacy, immunogenicity, clearance rate, stability, solubility, pharmacokinetics and mode of action of the product. In most instances, these linked N-glycans are analyzed in their unconjugated form after endoglycosidase-mediated release

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Sugano, Wataru, Ryukichi Ryo, Nobuo Yamaguchi, and Yoichi Shibata. "Endoglycosidase H digestion of Yukb(Pena) alloantigen." Thrombosis Research 67, no. 2 (1992): 167–77. http://dx.doi.org/10.1016/0049-3848(92)90136-x.

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Tarentino, A. L., G. Quinones, L. M. Changchien, and T. H. Plummer. "Multiple endoglycosidase F activities expressed by Flavobacterium meningosepticum endoglycosidases F2 and F3. Molecular cloning, primary sequence, and enzyme expression." Journal of Biological Chemistry 268, no. 13 (1993): 9702–8. http://dx.doi.org/10.1016/s0021-9258(18)98405-x.

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10

Du, Jonathan J., Erik H. Klontz, Marcelo E. Guerin, Beatriz Trastoy, and Eric J. Sundberg. "Structural insights into the mechanisms and specificities of IgG-active endoglycosidases." Glycobiology 30, no. 4 (2019): 268–79. http://dx.doi.org/10.1093/glycob/cwz042.

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Abstract The conserved N-glycan on Asn297 of immunoglobulin G (IgG) has significant impacts on antibody effector functions, and is a frequent target for antibody engineering. Chemoenzymatic synthesis has emerged as a strategy for producing antibodies with homogenous glycosylation and improved effector functions. Central to this strategy is the use of enzymes with activity on the Asn297 glycan. EndoS and EndoS2, produced by Streptococcus pyogenes, are endoglycosidases with remarkable specificity for Asn297 glycosylation, making them ideal tools for chemoenzymatic synthesis. Although both enzyme

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Dissertations / Theses on the topic "Endoglycosidase"

1

Saskiawan, Iwan. "Studies on Syntheses of Glycosylated Bioactive Peptides Using Mold Endoglycosidase and Analyses of Their Bioactivities." 京都大学 (Kyoto University), 2004. http://hdl.handle.net/2433/147902.

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Baruah, Kavitha. "Structural biology of IgG Fc glycoforms." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:def683d3-aa06-41d9-9f28-29d21258bebe.

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The conserved N-linked glycosylation site on the Fc domain of IgG1 antibodies is essential for maintaining a functionally active conformation of the antibody. Different glycoforms of the Fc exhibit widely different effector functions. Similarly, therapeutic antibodies, with engineered glycosylation, exhibit altered binding to cellular Fc receptors (FcRs). Here, X-ray crystallographic structures were obtained for biosynthetic intermediate glycoforms of human IgG1 Fc bearing: unprocessed oligomannose-type, intermediate hybrid-type, and mature complex-type glycans. The fully processed Fc protein

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Bourgerie, Sylvain. "Evaluation des activités endoglycosidases : caractérisation d'une endo-N-acétyl-B-D-glucosaminidase de Stigmatella aurantiaca DW4." Limoges, 1993. http://www.theses.fr/1993LIMO0233.

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Le travail entrepris a pour but de comprendre le role biologique des endoglycosidases en tant que marqueurs d'evenements cellulaires. L'introduction vise a preciser les caracteristiques des endo-beta-n-acetylglucosaminidases qui constituent de precieux outils d'investigation de la structure et des fonctions des n-glycosylproteines. Peu de donnees sont disponibles sur le role biologique de ces enzymes. Dans le premier chapitre est rappele les methodes generalement employees pour determiner l'activite des endoglycosidases, les limites de ces methodes et le choix d'un glycopeptide commercial marq

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Nielsen, Timothy Clement. "Identification and characterisation of endoglycosidase activities towards dermatan sulphate by tandem mass spectrometry." 2009. http://hdl.handle.net/2440/54629.

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Dermatan sulphate (DS) is a sulphated glycosaminoglycan (GAG) that is widely distributed as proteoglycan throughout the extracellular matrix and at cell surfaces where it plays an important role in many key biological processes. The intra-cellular catabolism of DS commences with endohydrolysis of the polysaccharide chains to oligosaccharides, which are then sequentially degraded from the non-reducing terminus by lysosomal exoenzymes to monosaccharides and inorganic sulphate for transport out of the lysosome and re-utilisation by the cell. Both endo-β-N-acetylhexosaminidase (Hyal-1 hyaluronidas

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Nielsen, Timothy Clement. "Identification and characterisation of endoglycosidase activities towards dermatan sulphate by tandem mass spectrometry." Thesis, 2009. http://hdl.handle.net/2440/54629.

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Dermatan sulphate (DS) is a sulphated glycosaminoglycan (GAG) that is widely distributed as proteoglycan throughout the extracellular matrix and at cell surfaces where it plays an important role in many key biological processes. The intra-cellular catabolism of DS commences with endohydrolysis of the polysaccharide chains to oligosaccharides, which are then sequentially degraded from the non-reducing terminus by lysosomal exoenzymes to monosaccharides and inorganic sulphate for transport out of the lysosome and re-utilisation by the cell. Both endo-β-N-acetylhexosaminidase (Hyal-1 hyaluronidas

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Yu, Tao, and 喻韜. "Preparation of deglycosylated Hemagglutinin of Influenza A Virus through Soluble and Immobilized Endoglycosidases." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/00660122790370210761.

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碩士<br>國立清華大學<br>生物資訊與結構生物研究所<br>98<br>Glycosylation is one of the common modifications in eukaryotic cell and is important for protein structure and function. Therefore, scientists have been tring to figure out the connection between protein glycosylation and human diseases. However, for protein crystallography, the glycans on the protein make it more difficult to get glycoprotein crystals. Our goal is to utilize endoglycosidases to quickly and massively produce deglycosylated glycoprotein under native condition. Furthermore, a suitable method was applied to immobilize these endoglycosidases f

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Books on the topic "Endoglycosidase"

1

Roberts, David Alan. The purification and partial characterisation of human heparan sulphate endoglycosidase. University of Manchester, 1995.

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2

Endo, Masahiko, Sumihiro Hase, Kenji Yamamoto, and Keiichi Takagaki, eds. Endoglycosidases. Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/978-3-540-49752-3.

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1926-, Takahashi Noriko, and Muramatsu Takashi 1941-, eds. CRC handbook of endoglycosidases and glycoamidases. CRC Press, 1992.

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4

(Editor), Masahiko Endo, Kenji Yamamoto (Editor), Keiichi Takagaki (Editor), and Sumihiro Hase (Editor), eds. Endoglycosidases - Biochemistry, Biotechnology, Application. Springer, 2006.

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5

Masahiko, Endo, ed. Endoglycosidases: Biochemistry, biotechnology, application. Kodansha, 2006.

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Takahashi, Noriko. Handbook of Endoglycosidases and Glycoamidases. CRC Press, 1992.

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Book chapters on the topic "Endoglycosidase"

1

Wang, Lai-Xi, Suddham Singh, and Jiahong Ni. "Synthesis of Bioactive Glycopeptides through Endoglycosidase-Catalyzed Transglycosylation." In ACS Symposium Series. American Chemical Society, 2004. http://dx.doi.org/10.1021/bk-2004-0873.ch006.

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2

Bernard, D., B. Méhul, and R. Schmidt. "Update on desquamation and first evidence for the presence of endoglycosidase heparanase 1 in the human stratum corneum." In The Essential Stratum Corneum. CRC Press, 2002. http://dx.doi.org/10.1201/b14296-4.

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3

Li, Chao, and Lai-Xi Wang. "Endoglycosidases for the Synthesis of Polysaccharides and Glycoconjugates." In Advances in Carbohydrate Chemistry and Biochemistry. Elsevier, 2016. http://dx.doi.org/10.1016/bs.accb.2016.07.001.

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4

Alexander, Stephen, and John H. Elder. "[43] Endoglycosidases from Flavobacterium meningosepticum application to biological problems." In Complex Carbohydrates Part F. Elsevier, 1989. http://dx.doi.org/10.1016/0076-6879(89)79151-5.

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5

Laine, Roger A., Jennifer W. C. Lo, and Betty C. R. Zhu. "Catalytically Inactive Endoglycosidases as Microbial Diagnostic Reagents: Chitinases and Lysozymes as Fungal and Bacterial Capture/Label Agents." In Lectins. Elsevier, 2007. http://dx.doi.org/10.1016/b978-044453077-6/50016-8.

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Conference papers on the topic "Endoglycosidase"

1

"Endoglycosidase expression in pubocervical fascia is up-regulated in menopause patients with severe pelvic organs prolapse." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-253.

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2

Fujita, Kiyotaka, Kazuo Kobayashi, Makoto Takeuchi, Hidehiko Kumagai, and Kenji Yamamoto. "ENZYMATIC SYNTHESIS OF NEO-GLYCOPROTEIN; A COMPLEX-TYPE OLIGOSACCHARIDE CONVERTING FROM HIGH MANNOSE-TYPE USING ENDOGLYCOSIDASE." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.734.

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3

Polack, B., A. Duperray, and R. Berthier. "PLATELET AND ENDOTHELIAL CELL CYTOADHESINS ARE BIOSYNTHESIZED AND PROCESSED VIA SIMILAR PATHWAYS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642815.

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The cytoadhesin family represents a group of heterodimeric adhesion receptors with common structural, fonctional and immunochemical properties. Platelet and endothelial cell (EC) GPIIbIII a related proteins exemplify two members of this family. In the present study the biosynthesis and processing of EC GPIIbIII a were examined and compared with that of platelet GPIIbIIIa to verify whether the diversity of these cytoadhesins was related to post translational events.Endothelial cells of human umbilical cord vein origin were metabolicaly labeled with 35S-methionine. The newly synthesized proteins

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Marquerie, G., A. Duperray, G. Uzan, and R. Berthier. "BIOSYNTHETIC PATHWAYS OF THE PLATELET FIBRINOGEN RECEPTOR IN HUMAN MEGAKARYOCYTES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642954.

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Interaction between cells and between cells and extracellular matrices are critical for a number of biological processes, including organ development, cell differenciation, cell motility, and the inimune' response. These interactions are mediated by a family of adhesion receptors that recognize short sequences such as Arg-Gly-Asp (RGD). These receptors share similar structural properties. They are heterodimers composed of a and B subunits and sometime express common epitopes. This suggests that the structural and functional relationship of these receptors may result from the transcription of r

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