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Biotinylated liposomes, binding

Biotinylated liposomes usually are created by modification of PE components with an amine-reactive biotin derivative, for example NHS-LC-Biotin (Chapter 11, Section 1). The NHS ester reacts with the primary amine of PE residues, forming an amide bond linkage (Figure 22.19). A better choice of biotinylation agent may be to use the NHS-PEG -biotin compounds (Chapter 18), because the hydrophilic PEG spacer provides better accessibility in the aqueous environment than a hydrophobic biotin spacer. Since the modification occurs at the hydrophilic end of the phospholipid molecule, after vesicle formation the biotin component protrudes out from the liposomal surface. In this configuration, the surface-immobilized biotins are able to bind (strept)avidin molecules present in the outer aqueous medium. [Pg.883]

Hashimoto, K., Loader, J.E., and Kinsky, S.C. (1986) Iodoacetylated and biotinylated liposomes Effect of spacer length on sulfbydryl ligand binding and avidin precipitability. Biochim. Biophys. Acta 856, 556-565. [Pg.1071]


See other pages where Biotinylated liposomes, binding is mentioned: [Pg.883]    [Pg.574]    [Pg.1145]    [Pg.554]    [Pg.460]    [Pg.248]    [Pg.69]    [Pg.71]    [Pg.379]    [Pg.465]    [Pg.884]    [Pg.347]    [Pg.314]    [Pg.575]    [Pg.492]    [Pg.119]    [Pg.188]    [Pg.315]    [Pg.555]    [Pg.324]    [Pg.324]    [Pg.207]    [Pg.207]    [Pg.773]    [Pg.609]    [Pg.117]    [Pg.433]    [Pg.69]    [Pg.203]   
See also in sourсe #XX -- [ Pg.1145 ]




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