Avidity Mechanism of Dendrimer–Folic Acid Conjugates
Author(s) -
Mallory A. van Dongen,
Justin E. Silpe,
Casey A. Dougherty,
Ananda Kumar Kanduluru,
Seok Ki Choi,
Bradford G. Orr,
Philip S. Low,
Mark M. Banaszak Holl
Publication year - 2014
Publication title -
molecular pharmaceutics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.13
H-Index - 127
eISSN - 1543-8392
pISSN - 1543-8384
DOI - 10.1021/mp5000967
Subject(s) - conjugate , avidity , dendrimer , chemistry , folic acid , ligand (biochemistry) , plasma protein binding , biochemistry , combinatorial chemistry , biophysics , receptor , antibody , biology , medicine , mathematical analysis , mathematics , immunology
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.
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