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Liposome glycolipids

Phospholipids are a major component of all biological membranes together with glycolipids and cholesterol. Due to their polar nature, i.e. hydrophilic head and hydrophobic tail, phospholipids form in water vesicles or liposomes. [Pg.970]

Figure 22.15 Glycolipid components included in liposome construction may be used to couple antibody molecules by using conjugates of lectins with the proper specificity for binding the sugar groups. Figure 22.15 Glycolipid components included in liposome construction may be used to couple antibody molecules by using conjugates of lectins with the proper specificity for binding the sugar groups.
Periodate-oxidize a liposome suspension containing glycolipid components according to Section 2 (this chapter). Adjust the concentration of total lipid to about 5mg/ml. [Pg.893]

Figure 22.25 Glycolipids incorporated into liposomes may be oxidized with periodate to produce aldehydes suitable for coupling proteins via reductive amination. Figure 22.25 Glycolipids incorporated into liposomes may be oxidized with periodate to produce aldehydes suitable for coupling proteins via reductive amination.
Glycolipid incorporated liposomes have found extensive use as sensors for the detection of Escherichia coli bacteria. Liposomes prepared using a diacetylene and a glucosyl lipid underwent a chromatic transition upon the addition of E. coli (Ma et al. 1998). The chromatic transition is sensitive to the diyne and glycolipid stmc-ture (Ma et al. 2000). An optimized vesicle assembly, consisting of a maltotriosyl lipid, phospholipid, and diyne, detected E. coli at a concentration of 2x10 cells/mL... [Pg.313]

Su et al. 2005). Mannosyl lipid containing liposomes have also been used for this purpose (Zhang et al. 2005). The glycolipids are presumed to interact with lectins present on the surface of the bacterial cells. [Pg.314]

Measurements of the quantities of glycolipids inserted into the membrane have also been reported by a technique based on the use of C-labeled lipid anchors. In this method, the carbohydrate (a-o-Man) was covalently coupled to the anchor at the surface of a pre-formed vesicle. Indeed, the liposome structure was shown to remain intact in the treatment. Nevertheless, the measurement of the incorporated mannose was performed after separation of bound and unbound material by centrifugation. The yields of coupling were shown to increase with the increase of the initial mannose/ C-anchor ratio, but non covalent insertions were displayed at high initial mannose concentrations. Therefore, the aforementioned method was not as accurate as could have been expected for the use of radioactive materials [142]. Radiolabeled phospholipids were also used for such determinations thus the amounts of glycosphingolipids incorporated into liposomes were quantified by the use of H-phospholipids whereas the amounts of glycolipids were determined by a sphingosine assay [143]. [Pg.297]

Prepare a 5 mg/ml liposome construction in 20 mM sodium phosphate, 0.15 M NaCl, pH 7.4, containing, on a molar ratio basis, a mixture of PC cholesterol PG other glycolipids of 8 10 1 2. The other glycolipids that can be incorporated include phosphatidyl inositol, lactosylceramide, galactose cerebroside, or various gangliosides. Other liposome compositions may be used, for example, recipes without cholesterol, as long as a periodate-oxidizable component... [Pg.561]


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See also in sourсe #XX -- [ Pg.469 ]




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