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Synthesis and Detection of BODIPY‐, Biotin‐, and 19 F‐ Labeled Single‐Entity Dendritic Heparan Sulfate Mimetics

Title: Synthesis and Detection of BODIPY‐, Biotin‐, and 19 F‐ Labeled Single‐Entity Dendritic Heparan Sulfate Mimetics
Authors: Spijkers‐Shaw, Sam; Devlin, Rory; Shields, Nicholas J.; Feng, Xiang; Peck, Tessa; Lenihan‐Geels, Georgia; Davis, Connor; Young, Sarah L.; La Flamme, Anne C.; Zubkova, Olga V.
Contributors: Ministry of Business, Innovation and Employment; Health Research Council of New Zealand
Source: Angewandte Chemie ; volume 136, issue 13 ; ISSN 0044-8249 1521-3757
Publisher Information: Wiley
Publication Year: 2024
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Heparin and heparan sulfate (HS) are naturally occurring mammalian glycosaminoglycans, and their synthetic and semi‐synthetic mimetics have attracted significant interest as potential therapeutics. However, understanding the mechanism of action by which HS, heparin, and HS mimetics have a biological effect is difficult due to their highly charged nature, broad protein interactomes, and variable structures. To address this, a library of novel single‐entity dendritic mimetics conjugated to BODIPY, Fluorine‐19 ( 19 F), and biotin was synthesized for imaging and localization studies. The novel dendritic scaffold allowed for the conjugation of labeling moieties without reducing the number of sulfated capping groups, thereby better mimicking the multivalent nature of HS‐protein interactions. The 19 F labeled mimetics were assessed in phantom studies and were detected at concentrations as low as 5 mM. Flow cytometric studies using a fluorescently labeled mimetic showed that the compound associated with immune cells from tumors more readily than splenic counterparts and was directed to endosomal‐lysosomal compartments within immune cells and cancer cells. Furthermore, the fluorescently labeled mimetic entered the central nervous system and was detectable in brain‐infiltrating immune cells 24 hours after treatment. Here, we report the enabling methodology for rapidly preparing various labeled HS mimetics and molecular probes with diverse potential therapeutic applications.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/ange.202316791
Availability: https://doi.org/10.1002/ange.202316791; https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202316791
Rights: http://creativecommons.org/licenses/by-nc-nd/4.0/
Accession Number: edsbas.FD5DACA6
Database: BASE