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Mannose-terminal

M. K. Bijsterbosch, W. Donker, H. Van de Bilt, S. Van Weely, T. J. Van Berkel, and J. M. Aerts, Quantitative analysis of the targeting of mannose-terminal glucocerebrosidase. Predominant uptake by liver endothelial cells, Eur. J. Biochem., 237 (1996) 344-349. [Pg.386]

Grabowski, G.A., N.W. Barton, G. Pastores, J.M. Dambrosia, T.K. Banerjee, M.A. McKee, C. Parker, R. Schiffmann, S.C. HiU, and R.O. Brady, Enzyme therapy in type 1 Gaucher disease comparative efficacy of mannose-terminated glucocerebrosidase... [Pg.255]

R. W. Jansen, G. Molema, T. L. Ching, R. Oosting, G. Harms, F. Moolenaar, M. J. Hardonk, and D. K. F. Meijer, Hepatic endocytosis of various types of mannose-terminated albumins. What is important, sugar recognition, net charge or the combination of these features, J. Biol. Chem. 266 3343-3348 (1991). [Pg.240]

Figure 3 Bar graph showing uptake of glncocengbrosldase by hcpaiocytcs and non-panoichymfll cells isolated from rat liver alter inflnion of 5.7 U of native or 5.0 U of mannose-terminal enzyme. (Adapted from Ref. 22.)... Figure 3 Bar graph showing uptake of glncocengbrosldase by hcpaiocytcs and non-panoichymfll cells isolated from rat liver alter inflnion of 5.7 U of native or 5.0 U of mannose-terminal enzyme. (Adapted from Ref. 22.)...
Rgura 6 Effect of weekly intravenous infusions of mannose-terminal glncocerebrosi-dase on senim acid phosphatase activity. Enzyme was administered as described in Figure... [Pg.269]

Medicine in New York using glucocerebrosidase that had been produced lecont-binantly in Chinese hamster ovary cells. The enzyme obtained from these cells was modified by exposure to the- same these cxogtycosidases used previously to produce mannose-terminal placental glucoceiebrosidase (Kg, 2). The clinical effectiveness of the recombinant macrophage-targeted enzyme was found to be... [Pg.278]

Y. Sato and E Bcutler. Binding, intenvUizatlofi, and degradation of mannose terminated glucocwebtosidase by macrophages, /, Clin. Invest. 91 1909 (1993). [Pg.281]

G. J. Murray, K. L, Oliver, F. 5. Jin, and R. O. Brady. Studies an the turnover of exogenous mannose-terminal glucocciebrosiJase in rat liver lymsomes. S. Cell... [Pg.281]

The clinical effects of mannose-terminal glucocerebrosidase were initially examined in eight patients with non-neuronopathic, type 1 Gaucher disease. Seven of the patients were either adolescents or adults, and one was a 4-year-old boy. A total dose of 190 U of enzyme was administered intravenously to each of these patients weekly over a 6-month period. A beneficial effect was clearly evident only in the youngest of the recipients [26]. A dramatic increase in... [Pg.265]

Figure 2 Production of mannose-terminal glucocerebrosidase by sequential deglycosylation of the native placental enzyme with exoglycosidases. Abbreviations as in Figure 1. (From Ref. 10.)... Figure 2 Production of mannose-terminal glucocerebrosidase by sequential deglycosylation of the native placental enzyme with exoglycosidases. Abbreviations as in Figure 1. (From Ref. 10.)...
Figure 4 Immunogold localization of mannose-terminal glucocerebrosidase in rat liver Kupffer cells 30 minutes after enzyme infusion. Gold particles are concentrated in the lysosomes. Lys = Lysosome M = mitochondrion Nuc = nucleus PM = plasma membrane. Original magnifications (A) x10,000 (B) x33,000. Bars = 1 pm. (From Ref. 24.)... Figure 4 Immunogold localization of mannose-terminal glucocerebrosidase in rat liver Kupffer cells 30 minutes after enzyme infusion. Gold particles are concentrated in the lysosomes. Lys = Lysosome M = mitochondrion Nuc = nucleus PM = plasma membrane. Original magnifications (A) x10,000 (B) x33,000. Bars = 1 pm. (From Ref. 24.)...
Figure 5 Effect of weekly intravenous infusions of mannose-terminal glucocere-brosidase on hemoglobin concentration in a 4-year-old boy with type 1 Gaucher disease. Solid black bars along the abscissa represent periods of enzyme treatment. A low dose of enzyme (9-12 U/kg) was administered between weeks 1 and 105 dosage was increased to 30 U/kg between weeks 131 and 320. Shaded areas represent the mean pretreatment and apparent steady-state values observed during the periods of low- and high-dose enzyme supplementation ( 1 SD). Normal range 11-15 g/dL. (From Ref. 10.)... Figure 5 Effect of weekly intravenous infusions of mannose-terminal glucocere-brosidase on hemoglobin concentration in a 4-year-old boy with type 1 Gaucher disease. Solid black bars along the abscissa represent periods of enzyme treatment. A low dose of enzyme (9-12 U/kg) was administered between weeks 1 and 105 dosage was increased to 30 U/kg between weeks 131 and 320. Shaded areas represent the mean pretreatment and apparent steady-state values observed during the periods of low- and high-dose enzyme supplementation ( 1 SD). Normal range 11-15 g/dL. (From Ref. 10.)...
Figure 9 Effect of mannose-terminal glucocerebrosidase on the bone marrow. Right posterior iliac crest biopsy specimens were obtained before (Pre) and after (Post) 3-1/2 years of treatment with high-dose enzyme supplementation. Marked clearing of the Gaucher cell infiltrate is evident in the posttreatment specimen. Original magnification x8. (From Ref. 28.)... Figure 9 Effect of mannose-terminal glucocerebrosidase on the bone marrow. Right posterior iliac crest biopsy specimens were obtained before (Pre) and after (Post) 3-1/2 years of treatment with high-dose enzyme supplementation. Marked clearing of the Gaucher cell infiltrate is evident in the posttreatment specimen. Original magnification x8. (From Ref. 28.)...
Figure 11 Enzymatic activity profile of mannose-terminal glucocerebrosidase in plasma of a boy with Gaucher disease. Enzyme was infused over 4 hours at a constant rate of 12.25 U/kg. A steady-state value of 10.6 mU/mL was achieved during the first hour. When the infusion was terminated at 240 minutes, enzyme was cleared from the plasma by a first-oider process with an elimination half-life of 6.3 minutes. The dashed line represents the activity profile calculated from the observed kinetic constants. Figure 11 Enzymatic activity profile of mannose-terminal glucocerebrosidase in plasma of a boy with Gaucher disease. Enzyme was infused over 4 hours at a constant rate of 12.25 U/kg. A steady-state value of 10.6 mU/mL was achieved during the first hour. When the infusion was terminated at 240 minutes, enzyme was cleared from the plasma by a first-oider process with an elimination half-life of 6.3 minutes. The dashed line represents the activity profile calculated from the observed kinetic constants.
G. J. Murray and F. S. Jin. Immunoelectron microscopic localization of mannose-terminal glucocerebrosidase in lysosomes of rat liver Kupffer cells. J. Histochem. Cytochem. 43 149 (1995). [Pg.281]

Mannose-terminating compounds made in connection with glycoprotein work have the sugar either or linked through 0-4 of chitobiose. The first of these reports exemplifies the use of polymer-supported reactions. Chemical and enzymic methods were used in the production of the latter trimer. [Pg.63]

Mannose-terminating compounds to have been described ate 17, which is the Le determinant linked to a linear mannotriose, and 18 with two lactosamine... [Pg.73]

Another interesting application of specific interactions in SAMs is the use of ligand-derivatized thiols to build up complex biosupramolecular architectures via molecular recognition-driven processes. Typical examples include the use of biotin- and mannose-terminated SAMs to biorecognize and assemble streptavidin and concanavalin A protein layers, respectively, on metal surfaces with diverse purposes (Figure 12). " ... [Pg.2781]

Dechtrirat, D., et al. Hybrid material for protein sensing based on electiosynthesized mip on a mannose terminated self-assembled monolayer. Adv. Funct. Mater. 24(15), 2233-2239 (2014)... [Pg.537]


See other pages where Mannose-terminal is mentioned: [Pg.193]    [Pg.361]    [Pg.116]    [Pg.256]    [Pg.265]    [Pg.524]    [Pg.526]    [Pg.405]    [Pg.170]    [Pg.194]    [Pg.264]    [Pg.265]    [Pg.266]    [Pg.278]    [Pg.281]    [Pg.421]    [Pg.20]    [Pg.45]    [Pg.33]    [Pg.1223]    [Pg.1636]   


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Terminal mannose residue

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