Self-assembled nanostructures hit their target
A tiny therapeutic delivery system that can control the body’s ability to manufacture proteins has been developed by Saudi Arabia's King Abdullah University of Science and Technology (KAUST) researchers.
Genes contain the instructions for manufacturing the proteins that make up our body. Genetic information is translated into the proteins needed to build living cells through a transcription process in which DNA’s genetic code is copied into a large molecule known as messenger RNA (mRNA).
This transcription process can be altered by introducing short double-strands of RNA, referred to as small interfering RNA (siRNA), which binds to the mRNA and inhibits the expression of particular genes. Harnessing this RNA interference for therapeutic applications is difficult and requires a material that can protect the siRNA as it travels through the bloodstream, helping it to penetrate the cell’s outer membrane and deliver it to its target location.
“Delivery of RNA is very tricky as it can be readily digested by cells. Better vehicles are needed so more RNA can be delivered in order to edit genes,” says Niveen Khashab from the KAUST Smart Hybrid Materials Laboratory.
Khashab and her colleagues have now demonstrated biocompatible nanostructures for delivering siRNA and efficiently silencing genes1. They combined the macromolecule histidine-capped-9,10-dialkoxy-anthracene (HDA) and siRNA in water. They observed the self-assembly of spherical nanoparticles when the water was slightly acidic, but not when it was pH neutral.
Khashab explains that these nanospheres are created by the electrostatic interaction between the positively charged HDA and negatively charged RNA, and then the two long arms of the HDA supramolecular wrap around the siRNA to protect it.
“Our organic linker is able to interact with genetic materials by hydrogen bonds and form a delivery vehicle,” explains Khashab. “The approach is scalable and creates reproducible amounts of encapsulated RNA; it is also biocompatible and safe.”
The nanoparticles could also be activated with visible light. When irradiated by green radiation while in the presence of an acidic fluorescent compound, known as eosin, the sphere disassembles and releases the siRNA.
The team showed the effectiveness of the nanoparticle for drug delivery on B-cell lymphoma 2, an mRNA molecule that creates proteins for regulating cell death. They showed that their nanostructures enhance the gene-silencing efficacy and led to gene knockdown of more than 90 percent after exposure to visible-light.
“The next step is to tweak the design to deliver other cargo molecules such as protein and improve the light response to higher wavelength in the near infrared,” says Khashab.
Patil, S. P., Moosa, B. A., Alsaiari, S., Alamoudi, K., Alshamsan, A., et al. Supramolecular self-assembly of histidine-capped-dialkoxy-anthracene: A visible-light-triggered platform for facile siRNA delivery. Chemistry - A European Journal advance online publication, 28 July 2016 (doi: 10.1002/chem.201601442)
