Development of a Platform of Antibody-Presenting Liposomes

Biointerphases

article

Boris Garnier¹  Sisareuth Tan¹  Céline Gounou¹  Alain R. Brisson¹  Jeanny Laroche-Traineau²  Marie-Josée Jacobin-Valat²  Gisèle Clofent-Sanchez² 

[1] CNRS-University Bordeaux1-ENITAB;CNRS-University Bordeaux Segalen

关键词: Atherosclerotic Plaque;    Dynamic Light Scattering;    Quartz Crystal Microbalance;    Trisodium Citrate;    Iron Oxide Particle;   

DOI  :  10.1007/s13758-011-0011-9

学科分类：基础医学

来源: SpringerOpen

【 摘 要 】

Antibody-presenting liposomes present high interest as drug delivery systems. The association of antibodies to liposomes is usually realized by covalent coupling of IgGs or their antigen-binding fragments to lipid polar head groups by means of hetero-bifunctional crosslinkers. We present here an original platform of IgG-presenting liposomes which is based on a fusion protein between Annexin-A5 (Anx5) and the IgG-binding ZZ repeat derived from Staphylococcus aureus protein A. The Anx5ZZ fusion protein acts as a bi-functional adaptor that anchors IgGs to liposomes in a non covalent and highly versatile manner. The interactions between IgGs, Anx5ZZ and liposomes were characterized by PAGE, dynamic light scattering and fluorescence quenching assays, establishing that binding of Anx5ZZ to IgGs and of Anx5ZZ–IgG complexes to liposomes is complete with stoichiometric amounts of each species. We found that the sequence of assembly is important and that Anx5ZZ–IgG complexes need to be formed first in solution and then adsorbed to liposomes in order to avoid aggregation. The targeting capacity of Anx5ZZ–IgG-functionalized liposomes was demonstrated by electron microscopy on an ex vivo model system of atherosclerotic plaques. This study shows that the Anx5ZZ adaptor constitutes an efficient platform for functionalizing liposomes with IgGs. This platform may present potential applications in molecular imaging and drug delivery.

【 授权许可】

CC BY