Synthesis of a Fluorescent Analogue of Paclitaxel That Selectively Binds Microtubules and Sensitively Detects Efflux by P-Glycoprotein.
Molly M LeeZhe GaoBlake R PetersonPublished in: Angewandte Chemie (International ed. in English) (2017)
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).
Keyphrases
- living cells
- fluorescent probe
- flow cytometry
- single molecule
- quantum dots
- heavy metals
- induced apoptosis
- oxidative stress
- small molecule
- drug induced
- squamous cell carcinoma
- cell cycle arrest
- cell death
- squamous cell
- signaling pathway
- electronic health record
- oxide nanoparticles
- tandem mass spectrometry
- liquid chromatography