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GPI-anchor

AChE-E (in blue) GPI-anchored dimers to plasma membranes in mammalian muscles, erythrocytes and lymphocytes. [Pg.360]

GPI anchoring is a posttranslational modification occurring in the endoplasmic reticulum where preassembled GPI anchor precursors are transferred to proteins bearing a C-terminal GPI signal sequence. The GPI anchor precursors are synthesized in the endoplasmic reticulum by sequential addition of sugar and other components to phosphatidylinositol. Protein GPI anchors are ubiquitous in eukaryotic cells. In mammalian cells, GPI anchored proteins are often found in lipid rafts which are subdomains of the plasma membrane, containing various signaling components. [Pg.557]

Lipidation -acylation TV -myristoylation Myristoy-lation S-prenylation Prenylation Palmitoylation Isoprenylation GPI anchors Glypiation... [Pg.691]

GPI anchor Complex structure includes Carboxyl-term in us... [Pg.691]

GPI-anchored proteins constitute a quite diverse family of cell-surface molecules that participate in such processes as nutrient uptake, cell adhesion, and membrane signaling events [3]. All GPI-linked proteins are destined for the cell surface via trafficking through the secretory pathway, where they acquire the... [Pg.692]

Paroxysmal nocturnal hemoglobinuria (MIM 311770) Mutation resulting in deficient attachment of the GPI anchor to certain proteins of the red cell membrane... [Pg.432]

Paroxysmal nocturnal hemoglobinemia (MIM 311770) Mutations in the PIG-A gene, affecting synthesis of GPI-anchored proteins... [Pg.610]

Of the integral membrane proteins referred to above, Hll has a distinct transmembrane region (Smith et al, 1997), the GA1 proteins are anchored via a glycosylinositolphospholipid (GPI) membrane anchor on p52, with p46 being held in place by as yet undefined interactions (Jasmer et al., 1996). The P150 complex is anchored by a membrane (GPI) anchor on the 53 kDa component which forms non-covalent associations with the 45 and 53 kDa components (Rocha and Munn, 1997). The means by which... [Pg.270]

Kenworthy, A. K., Petranova, N. and Edidin, M. (2000). High resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes. Mol. Biol. Cell 11, 1645-55. [Pg.70]

Add an aliquot of the DSS or BS3 solution to the reaction medium to obtain a final concentration of 0.5-5mM. Note Simons et al. (1999) successfully used a concentration of 0.5 mM BS3 with Madin-Darby canine kidney (MDCK) cells permanently expressing a GPI-anchored form of growth hormone decay accelerating factor (GH-DAF) to crosslink the protein interaction complexes on the cell surfaces. [Pg.1007]

Friedrichson, T., and Kurzchalia, T.V. (1998) Microdomains of GPI-anchored proteins in living cells revealed by crosslinking. Nature 394(6695), 802-805. [Pg.1064]

Much of the plasma membrane cholesterol is removed by incubating cells with P-methylcyclodextrin for several hours. Cells remain viable after this treatment but the raft fraction is reduced and it is inferred that the depleted proteins are normally associated with cholesterol-dependent lipid rafts. Some, but not all, glycosylphosphatidylinositol (GPI)-anchored proteins are recovered in the fractions defined by this procedure. [Pg.28]

GPI-anchored proteins (GP-APs) are synthesized in the cytoplasm and their transport into the ER occurs during the process of acquiring a GPI anchor, which is ultimately sorted into the outer leaflet of plasma membranes [24], A FRET study of fluorophore-labeled GPI-APs in cultured... [Pg.28]

Sharma, P., Varma, R., Sarasij, R. C., Gousset, K., Krishnamoorthy, G. and Rao M, Mayor S. Nanoscale organization of multiple GPI-anchored proteins in living cell membranes. Cell 116 577-589, 2004. [Pg.32]

A bacterial phosphatidylinositol specific phospholipase C (PI-PLC) had been available for many years before it was demonstrated to strip a number of membrane-bound proteins from eukaryotic cell surfaces [1], Such proteins are anchored by a PI moiety in which the 6 position of inositol is glycosidically linked to glucosamine, which in turn is bonded to a polymannan backbone (Fig. 3-10). The polysaccharide chain is joined to the carboxyl terminal of the anchored protein via amide linkage to ethanolamine phosphate. The presence of a free NH2 group in the glucosamine residue makes the structure labile to nitrous acid. Bacterial PI-PLC hydrolyzes the bond between DAG and phosphati-dylinositols, releasing the water-soluble protein polysac charide-inositol phosphate moiety. These proteins are tethered by glycosylphosphatidylinositol (GPI) anchors. [Pg.47]

Medof, M. E., Nagargian, S. and Tykocinski, M. L. Cell-surface engineering with GPI-anchored proteins. FASEB J. 10 574-586,1996. [Pg.49]

Members of this family of molecules may have only one Ig-like domain, as is the case for the myelin protein P0, or, as for most of the family, have many Ig domains. In addition to the subclassification of Ig domains into V-, C- and C2-like domains, Ig family members can be broadly divided into three general classes [8] (a) those that have only Ig-like domains (b) those that have Ig domains and additional domains that resemble regions of the ECM component fibronectin, termed FN-like domains and (c) those that have Ig domains and motifs other than FN-like domains. Moreover, any one Ig family member may have many isoforms, which may differ in the length of the cytoplasmic domain, in their post-translational modifications and whether they are membrane-spanning or glycosylphos-phatidylinositol (GPI)-anchored proteins (see Box 3-1). Also, additional amino acid sequences inserted in the extracellular domain may distinguish isoforms of a particular IgCAM. While it is not known how the majority... [Pg.112]

Other pinocytotic pathways also exist that do not depend on either caveolae or clathrin, although these are not as well defined [55]. Specific receptors continue to be internalized in the absence of clathrin or caveolin and these pathways can be monitored by following glycosyl phos-phatidylinositol (GPI (-anchored proteins. Nonclathrin, noncaveolin pathways may also be responsible for the reuptake of membrane in neuroendocrine cells after stimulated secretion. Some, but not all, of these pathways appear to require dynamin. [Pg.153]


See other pages where GPI-anchor is mentioned: [Pg.279]    [Pg.359]    [Pg.557]    [Pg.559]    [Pg.693]    [Pg.693]    [Pg.844]    [Pg.986]    [Pg.1493]    [Pg.1493]    [Pg.512]    [Pg.518]    [Pg.522]    [Pg.528]    [Pg.358]    [Pg.271]    [Pg.294]    [Pg.237]    [Pg.47]    [Pg.47]    [Pg.49]    [Pg.49]    [Pg.49]    [Pg.428]    [Pg.576]    [Pg.792]    [Pg.796]    [Pg.796]   
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See also in sourсe #XX -- [ Pg.213 , Pg.214 , Pg.222 ]

See also in sourсe #XX -- [ Pg.206 ]

See also in sourсe #XX -- [ Pg.213 , Pg.214 , Pg.222 ]




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Analysis of the GPI Anchor

Anchors, membrane for proteins glycosylphosphatidylinositol (GPI

Biosynthesis of GPI-anchored

Biosynthesis of GPI-anchored proteins

GPI anchored protein

GPI anchors attachment

GPI anchors biosynthesis

GPI-anchored mannoproteins

Glycophosphatidylinositol (GPI) Anchors

Synthesis of Plasmodium falciparum GPI Anchor

Synthesis of Trypanosoma cruzi GPI Anchor

Synthesis of a Human Lymphocyte CD52 Antigen GPI Anchor

Synthesis of a Human Sperm CD52 Antigen GPI Anchor

Synthesis of the Rat Brain Thy-1 GPI Anchor

Synthesis of the Yeast GPI Anchor

The Biosynthesis of GPI Anchors

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