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Vesicles, cross-linked

Figure 2. Graphic representation of vesicle cross-linking (A) complete cross -linking (B) partial cross-linking (C) destructive cross-linking to vesicle structure. (See page 9 of color inserts.)... Figure 2. Graphic representation of vesicle cross-linking (A) complete cross -linking (B) partial cross-linking (C) destructive cross-linking to vesicle structure. (See page 9 of color inserts.)...
Dephosphorylated synapsin inhibits axonal transport of MBOs in isolated axoplasm, while phosphorylated synapsin at similar concentrations has no effect [21]. When a synaptic vesicle passes through a region rich in dephosphorylated synapsin, it may be cross-linked to the available MF matrix by synapsin. Such cross-linked vesicles would be removed from fast axonal transport and are effectively targeted to a synapsin- and MF-rich domain, the presynaptic terminal. [Pg.493]

Figure 18.16 Hypothetical model for the metallobiology of AP in Alzheimer s disease. (From Bush, 2003. Copyright 2003, with permission from Elsevier.) The proposed sequence of events (1) concentration of iron and copper increase in the cortex with aging. There is an overproduction of APP and AP in an attempt to suppress cellular metal-ion levels. (2) Hyper-metallation of AP occurs which may facilitate H202 production. (3) Hyper-metallated AP reacts with H202 to generate oxidized and cross-linked forms, which are liberated from the membrane. (4) Soluble AP is released from the membrane and is precipitated by zinc which is released from the synaptic vesicles. Oxidized AP is the major component of the plaque deposits. (5) Oxidized AP initiates microglia activation. (6) H202 crosses cellular membranes to react with Cu and Fe, and generate hydroxyl radicals which oxidize a variety of proteins and lipids. Figure 18.16 Hypothetical model for the metallobiology of AP in Alzheimer s disease. (From Bush, 2003. Copyright 2003, with permission from Elsevier.) The proposed sequence of events (1) concentration of iron and copper increase in the cortex with aging. There is an overproduction of APP and AP in an attempt to suppress cellular metal-ion levels. (2) Hyper-metallation of AP occurs which may facilitate H202 production. (3) Hyper-metallated AP reacts with H202 to generate oxidized and cross-linked forms, which are liberated from the membrane. (4) Soluble AP is released from the membrane and is precipitated by zinc which is released from the synaptic vesicles. Oxidized AP is the major component of the plaque deposits. (5) Oxidized AP initiates microglia activation. (6) H202 crosses cellular membranes to react with Cu and Fe, and generate hydroxyl radicals which oxidize a variety of proteins and lipids.
The process utilizing supramolecular organization involves pore expansion in silicas. A schematic view of such micelles built from the pure surfactant and those involving in addition n-alkane is shown in Figure 4.9. Another example of pore creation provides a cross-linking polymerization of monomers within the surfactant bilayer [30]. As a result vesicle-templated hollow spheres are created. Dendrimers like that shown in Figure 4.10 exhibit some similarity to micellar structures and can host smaller molecules inside themselves [2c]. Divers functionalized dendrimers that are thought to present numerous prospective applications will be presented in Section 7.6. [Pg.77]

The so-called coated vesicles are an example of an enveloped membrane3). A phospholipid vesicle within a cell is coated by a polypeptide and resembles a foot-ball in a net. A comparable feature of membrane coating is found in cell walls of bacteria4 . These cell walls consist of polysaccharides which are cross-linked by oligopeptides. It is remarkable that this extreme stabilization by an exogenous support is found in bacteria. As parasites in foreign tissues, they have to be especially resistant. [Pg.3]

The down-regulation of receptors by endocytosis. The hormone-mediated loss of receptors is often referred to as down-regulation. Continuous activation of receptors by hormone often leads to patching, a clustering of receptors as if they were cross-linked. Endocytosis of the patches removes them from the cell surface. The endocytotic vesicles, sometimes called receptosomes, fuse with lysosomes, where the contents are degraded by the lysosomal enzymes. Receptosomes also may allow entry of receptors into other cell compartments, such as the nucleus, by fusing with these organelles. [Pg.589]

Hackett, C.S. Strittmatter, P. (1984). Covalent cross-linking of the active sites of vesicle-bound cytochrome b5 and NADH-cytochrome b5 reductase. Journal of Biological Chemistry 259, 3275-82. [Pg.72]


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See also in sourсe #XX -- [ Pg.53 ]




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