Interaction of a Triantennary Quinoline Glycoconjugate with the Asialoglycoprotein Receptor
Autor: | Chandra Sova Mandi, Tanusree Das, Tridib Mahata, Sayanika Banerjee, Partha Chakrabarti, Sougata Niyogi, Sanjay Dutta, Subhadeep Palit |
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Rok vydání: | 2021 |
Předmět: |
Glycoconjugate
Asialoglycoprotein Receptor Endocytosis 01 natural sciences Biochemistry chemistry.chemical_compound Structure-Activity Relationship Cell Line Tumor Drug Discovery Humans General Pharmacology Toxicology and Pharmaceutics Cytotoxicity Receptor Pharmacology chemistry.chemical_classification Dose-Response Relationship Drug Molecular Structure 010405 organic chemistry Organic Chemistry Quinoline 0104 chemical sciences 010404 medicinal & biomolecular chemistry chemistry Drug delivery Quinolines Molecular Medicine Asialoglycoprotein receptor Glycoconjugates Intracellular |
Zdroj: | ChemMedChem. 16(14) |
ISSN: | 1860-7187 |
Popis: | Targeted intracellular delivery is an efficient strategy for developing therapeutics against cancer and other intracellular infections. Nonspecific drug delivery shows limited clinical applications owing to high dosage, cytotoxicity, nonspecific action, high cost, etc. Therefore, targeted delivery of less cytotoxic drug candidates to hepatocytes through ASGPR-mediated endocytosis could be an efficient strategy to surmount the prevailing shortcomings. In the present work, the gene encoding ASGPR-H1-CRD was amplified from Huh7 cells, cloned into pET 11a vector, and the ASGPR-H1-CRD protein was expressed and purified from E. coli. A novel triantennary galactose-conjugated quinoline derivative 4 was synthesized that demonstrates 17-fold higher binding affinity to isolated ASGPR-H1-CRD protein receptor (Kd ∼54 μM) in comparison to D-galactose (Kd ∼900 μM). Moreover, micro-calorimetric studies for the interaction of glycoconjugate 4 with ASGPR protein on live hepatocytes showed notable thermal response in case of ASGPR-containing Huh7 cells, in comparison to non-ASGPR Chang cells. These results might serve as an approach towards targeted delivery of small glycoconjugates to hepatocytes. |
Databáze: | OpenAIRE |
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