Synthesis of a Fluorescent Analogue of Paclitaxel That Selectively Binds Microtubules and Sensitively Detects Efflux by P-Glycoprotein

Molly M. Lee, Zhe Gao, Blake R. Peterson

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

The anticancer drug paclitaxel (Taxol) exhibits paradoxical and poorly understood effects against slow-growing tumors. To investigate its biological activity, fluorophores such as Oregon Green have been linked to this drug. However, this modification increases its polarity by approximately 1000-fold and reduces the toxicity of Taxol towards cancer cell lines by over 200-fold. To construct more drug-like fluorescent probes suitable for imaging by confocal microscopy and analysis by flow cytometry, we synthesized derivatives of Taxol linked to the drug-like fluorophore Pacific Blue (PB). We found that PB-Gly-Taxol bound the target protein β-tubulin with both high affinity in vitro and high specificity in living cells, exhibited substantial cytotoxicity towards HeLa cells, and was a highly sensitive substrate of the multidrug resistance transporter P-glycoprotein (P-gp).

Original languageEnglish
Pages (from-to)6927-6931
Number of pages5
JournalAngewandte Chemie - International Edition
Volume56
Issue number24
DOIs
StatePublished - Jun 6 2017

Keywords

  • antitumor agents
  • confocal microscopy
  • drug design
  • fluorescent probes
  • paclitaxel

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