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Cryptophane-Folate Biosensor for (129)Xe NMR

[Image: see text] Folate-conjugated cryptophane was developed for targeting cryptophane to membrane-bound folate receptors that are overexpressed in many human cancers. The cryptophane biosensor was synthesized in 20 nonlinear steps, which included functionalization with folate recognition moiety, s...

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Autores principales: Khan, Najat S., Riggle, Brittany A., Seward, Garry K., Bai, Yubin, Dmochowski, Ivan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306503/
https://www.ncbi.nlm.nih.gov/pubmed/25438187
http://dx.doi.org/10.1021/bc5005526
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author Khan, Najat S.
Riggle, Brittany A.
Seward, Garry K.
Bai, Yubin
Dmochowski, Ivan J.
author_facet Khan, Najat S.
Riggle, Brittany A.
Seward, Garry K.
Bai, Yubin
Dmochowski, Ivan J.
author_sort Khan, Najat S.
collection PubMed
description [Image: see text] Folate-conjugated cryptophane was developed for targeting cryptophane to membrane-bound folate receptors that are overexpressed in many human cancers. The cryptophane biosensor was synthesized in 20 nonlinear steps, which included functionalization with folate recognition moiety, solubilizing peptide, and Cy3 fluorophore. Hyperpolarized (129)Xe NMR studies confirmed xenon binding to the folate-conjugated cryptophane. Cellular internalization of biosensor was monitored by confocal laser scanning microscopy and quantified by flow cytometry. Competitive blocking studies confirmed cryptophane endocytosis through a folate receptor-mediated pathway. Flow cytometry revealed 10-fold higher cellular internalization in KB cancer cells overexpressing folate receptors compared to HT-1080 cells with normal folate receptor expression. The biosensor was determined to be nontoxic in HT-1080 and KB cells by MTT assay at low micromolar concentrations typically used for hyperpolarized (129)Xe NMR experiments.
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spelling pubmed-43065032015-12-01 Cryptophane-Folate Biosensor for (129)Xe NMR Khan, Najat S. Riggle, Brittany A. Seward, Garry K. Bai, Yubin Dmochowski, Ivan J. Bioconjug Chem [Image: see text] Folate-conjugated cryptophane was developed for targeting cryptophane to membrane-bound folate receptors that are overexpressed in many human cancers. The cryptophane biosensor was synthesized in 20 nonlinear steps, which included functionalization with folate recognition moiety, solubilizing peptide, and Cy3 fluorophore. Hyperpolarized (129)Xe NMR studies confirmed xenon binding to the folate-conjugated cryptophane. Cellular internalization of biosensor was monitored by confocal laser scanning microscopy and quantified by flow cytometry. Competitive blocking studies confirmed cryptophane endocytosis through a folate receptor-mediated pathway. Flow cytometry revealed 10-fold higher cellular internalization in KB cancer cells overexpressing folate receptors compared to HT-1080 cells with normal folate receptor expression. The biosensor was determined to be nontoxic in HT-1080 and KB cells by MTT assay at low micromolar concentrations typically used for hyperpolarized (129)Xe NMR experiments. American Chemical Society 2014-12-01 2015-01-21 /pmc/articles/PMC4306503/ /pubmed/25438187 http://dx.doi.org/10.1021/bc5005526 Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Khan, Najat S.
Riggle, Brittany A.
Seward, Garry K.
Bai, Yubin
Dmochowski, Ivan J.
Cryptophane-Folate Biosensor for (129)Xe NMR
title Cryptophane-Folate Biosensor for (129)Xe NMR
title_full Cryptophane-Folate Biosensor for (129)Xe NMR
title_fullStr Cryptophane-Folate Biosensor for (129)Xe NMR
title_full_unstemmed Cryptophane-Folate Biosensor for (129)Xe NMR
title_short Cryptophane-Folate Biosensor for (129)Xe NMR
title_sort cryptophane-folate biosensor for (129)xe nmr
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306503/
https://www.ncbi.nlm.nih.gov/pubmed/25438187
http://dx.doi.org/10.1021/bc5005526
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