Azulitox-A Pseudomonas aeruginosa P28-Derived Cancer-Cell-Specific Protein Photosensitizer.
Heinz Fabian RaberThomas HeerdeSuzanne Nour El DinCarolin FlaigFabienne HilgersNora BitzenhoferKarl-Erich JägerThomas DrepperKay-Eberhard GottschalkNicholas Emil BodenbergerTanja WeilDennis Horst KubiczekFrank RosenauPublished in: Biomacromolecules (2020)
Azulitox as a new fusion polypeptide with cancer cell specificity and phototoxicity was generated and is composed of a photosensitizer domain and the cell-penetrating peptide P28. The photosensitizer domain (EcFbFP) was derived from a bacterial blue-light receptor, which belongs to the family of light-oxygen-voltage proteins and produces reactive oxygen species (ROS) upon excitation. P28 is derived from the cupredoxin protein azurin that is known to specifically penetrate cancer cells and bind to the tumor suppressor protein p53. We show that the P28 domain specifically directs and translocates the fused photosensitizer into cancer cells. Under blue-light illumination, Azulitox significantly induced cytotoxicity. Compared to the extracellular application of EcFbFP, Azulitox caused death to about 90% of cells, as monitored by flow cytometry, which also directly correlated with the amount of ROS produced in the cells. Azulitox may open new avenues toward targeted polypeptide-photosensitizer-based photodynamic therapies with reduced systemic toxicity compared to conventional photosensitizers.
Keyphrases
- photodynamic therapy
- reactive oxygen species
- induced apoptosis
- flow cytometry
- pseudomonas aeruginosa
- cell cycle arrest
- cell death
- protein protein
- binding protein
- dna damage
- cancer therapy
- oxidative stress
- amino acid
- cell therapy
- signaling pathway
- high glucose
- escherichia coli
- small molecule
- biofilm formation
- endothelial cells
- cell proliferation
- diabetic rats
- energy transfer