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National Institute of Environmental Health Sciences

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Publication Detail

Title: A Modular Ionophore Platform for Liver-Directed Copper Supplementation in Cells and Animals.

Authors: Su, Timothy A; Shihadih, Diyala S; Cao, Wendy; Detomasi, Tyler C; Heffern, Marie C; Jia, Shang; Stahl, Andreas; Chang, Christopher J

Published In J Am Chem Soc, (2018 10 24)

Abstract: Copper deficiency is implicated in a variety of genetic, neurological, cardiovascular, and metabolic diseases. Current approaches for addressing copper deficiency rely on generic copper supplementation, which can potentially lead to detrimental off-target metal accumulation in unwanted tissues and subsequently trigger oxidative stress and damage cascades. Here we present a new modular platform for delivering metal ions in a tissue-specific manner and demonstrate liver-targeted copper supplementation as a proof of concept of this strategy. Specifically, we designed and synthesized an N-acetylgalactosamine-functionalized ionophore, Gal-Cu(gtsm), to serve as a copper-carrying "Trojan Horse" that targets liver-localized asialoglycoprotein receptors (ASGPRs) and releases copper only after being taken up by cells, where the reducing intracellular environment triggers copper release from the ionophore. We utilized a combination of bioluminescence imaging and inductively coupled plasma mass spectrometry assays to establish ASGPR-dependent copper accumulation with this reagent in both liver cell culture and mouse models with minimal toxicity. The modular nature of our synthetic approach presages that this platform can be expanded to deliver a broader range of metals to specific cells, tissues, and organs in a more directed manner to treat metal deficiency in disease.

PubMed ID: 30351140 Exiting the NIEHS site

MeSH Terms: Acetylgalactosamine/chemical synthesis; Acetylgalactosamine/chemistry; Acetylgalactosamine/metabolism*; Animals; Asialoglycoprotein Receptor/metabolism; Copper/administration & dosage*; Copper/pharmacokinetics*; Dietary Supplements*/analysis; Drug Carriers/chemical synthesis; Drug Carriers/chemistry; Drug Carriers/metabolism*; Drug Delivery Systems; Ionophores/chemical synthesis; Ionophores/chemistry; Ionophores/metabolism*; Liver/metabolism*; Mice

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