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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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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
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author 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.
author_facet 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.
author_sort van Dongen, Mallory A.
collection PubMed
description [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.
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spelling pubmed-40180992015-04-11 Avidity Mechanism of Dendrimer–Folic Acid Conjugates 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. Mol Pharm [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. American Chemical Society 2014-04-11 2014-05-05 /pmc/articles/PMC4018099/ /pubmed/24725205 http://dx.doi.org/10.1021/mp5000967 Text en Copyright © 2014 American Chemical Society
spellingShingle 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.
Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title_full Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title_fullStr Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title_full_unstemmed Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title_short Avidity Mechanism of Dendrimer–Folic Acid Conjugates
title_sort avidity mechanism of dendrimer–folic acid conjugates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018099/
https://www.ncbi.nlm.nih.gov/pubmed/24725205
http://dx.doi.org/10.1021/mp5000967
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