| Literature DB >> 28939491 |
Anna Ohradanova-Repic1, Eugénia Nogueira2, Ingrid Hartl3, Andreia C Gomes4, Ana Preto4, Eva Steinhuber3, Vanessa Mühlgrabner3, Marko Repic5, Mario Kuttke6, Alexander Zwirzitz3, Marek Prouza7, Miloslav Suchanek7, Gordana Wozniak-Knopp8, Vaclav Horejsi9, Gernot Schabbauer6, Artur Cavaco-Paulo10, Hannes Stockinger3.
Abstract
Liposomes functionalized with monoclonal antibodies or their antigen-binding fragments have attracted much attention as specific drug delivery devices for treatment of various diseases including cancer. The conjugation of antibodies to liposomes is usually achieved by covalent coupling using cross-linkers in a reaction that might adversely affect the characteristics of the final product. Here we present an alternative strategy for liposome functionalization: we created a recombinant Fab antibody fragment genetically fused on its C-terminus to the hydrophobic peptide derived from pulmonary surfactant protein D, which became inserted into the liposomal bilayer during liposomal preparation and anchored the Fab onto the liposome surface. The Fab-conjugated liposomes specifically recognized antigen-positive cells and efficiently delivered their cargo, the Alexa Fluor 647 dye, into target cells in vitro and in vivo. In conclusion, our approach offers the potential for straightforward development of nanomedicines functionalized with an antibody of choice without the need of harmful cross-linkers.Entities:
Keywords: Active targeting; Antibody engineering; Immunoliposome; Liposome functionalization; Recombinant Fab antibody fragment
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Year: 2017 PMID: 28939491 DOI: 10.1016/j.nano.2017.09.003
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307