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Avidity Mechanism of Dendrimer–Folic Acid Conjugates

[Image: see text] Multivalent conjugation of folic acid has been employed to target cells overexpressing folate receptors. Such polymer conjugates have been previously demonstrated to have high avidity to folate binding protein. However, the lack of a monovalent folic acid–polymer material has preve...

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Detalles Bibliográficos
Autores principales: van Dongen, Mallory A., Silpe, Justin E., Dougherty, Casey A., Kanduluru, Ananda Kumar, Choi, Seok Ki, Orr, Bradford G., Low, Philip S., Banaszak Holl, Mark M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018099/
https://www.ncbi.nlm.nih.gov/pubmed/24725205
http://dx.doi.org/10.1021/mp5000967
Descripción
Sumario:[Image: see text] Multivalent conjugation of folic acid has been employed to target cells overexpressing folate receptors. Such polymer conjugates have been previously demonstrated to have high avidity to folate binding protein. However, the lack of a monovalent folic acid–polymer material has prevented a full binding analysis of these conjugates, as multivalent binding mechanisms and polymer-mass mechanisms are convoluted in samples with broad distributions of folic acid-to-dendrimer ratios. In this work, the synthesis of a monovalent folic acid–dendrimer conjugate allowed the elucidation of the mechanism for increased binding between the folic acid–polymer conjugate and a folate binding protein surface. The increased avidity is due to a folate-keyed interaction between the dendrimer and protein surfaces that fits into the general framework of slow-onset, tight-binding mechanisms of ligand/protein interactions.