The ease by which mRNA-based drugs are taken up by cells in tissues is crucial to their therapeutic effectiveness.
Now, a new detection method developed by researchers at
'We have developed an automated process to monitor and test large numbers of different lipid nanoparticles simultaneously, which we hope will streamline the development of new medicines,' says
Messenger RNA, or mRNA, is the code used by cells to produce proteins. When it is introduced as a drug or a vaccine, it is interpreted by the cells as a set of instructions, to then use their own systems to produce the desired proteins.
mRNA-based technologies are being explored for their potential to help treat chronic diseases in various ways, such as by encoding therapeutic proteins, and potentially be tailored for specific tissues, for example to replace incorrect proteins or regulate cellular malfunctions that cause disease.
But there are several major challenges associated with this new technology. First, the cells must be 'tricked' into taking in the mRNA molecules. One of the most advanced ways of doing this is to pack the mRNA into a small droplet, known as a lipid nanoparticle. The nanoparticles enter cells in a large bubble called an endosome, which transports its contents to the cell's 'lysosomes', or degradation stations. The lipid nanoparticles containing the mRNA must exit the endosome at just the right moment, to reach the cell's cytoplasm, where the proteins are made, before the endosome reaches the degradation station. Otherwise, the mRNA will break down and no longer be able to work. This vital step is called 'endosomal escape' and timing it correctly is the most decisive factor for mRNA-based medicines to work.
Tracking the escape
The new study describes a method that the researchers developed to monitor and analyse the movement of the lipid nanoparticles through the cell using detectable fluorescent markers. In addition to being able to see if the lipid particle has been taken up by the cells, and the mRNA delivered is able to produce the encoded protein, the researchers also developed a marker to track precisely when and where endosomal escape has taken place, and in what quantity. This marker consists of a fluorescent version of the protein Galectin-9, which can be seen to accumulate when mRNA escapes endosomes.
'Instead of just seeing which lipid nanoparticles work best, we can now also understand what makes them work optimally, and use that knowledge to develop and test new improved nanoparticle formulations,' says
Elin Esbjorner, Associate Professor of Chemical Biology at
'To reduce the risk of side effects, such as the immune system being triggered by the lipid particles, we want to use the lowest possible dose. This is particularly true for diseases which require long term treatment. In those cases, it is vital that the moment of endosomal escape is optimally timed, to allow the mRNA to get out into the cytoplasm with maximum effect,' she says.
In addition to allowing the researchers to evaluate a large number of lipid particles at the same time, the new method can also help examine how efficiently the lipid particles are delivered and how well they function in different types of cells. This could allow for tailoring the drugs to target specific tissues, such as in the lungs or the liver.
'The lipid nanoparticles work differently in different cell types. A formulation that works well for delivery to liver cells, for example, could be significantly different in lung cells. Our new method could help us understand why such differences exist, and to harness this knowledge to design new lipid nanoparticles tailored for different targets in the body,' says Elin Esbjorner.
Read the scientific article in Nature Communications Biology:
A high-throughput Galectin-9 imaging assay for quantifying nanoparticle uptake, endosomal escape and functional RNA delivery
Read more about FoRmulaEx :
FoRmulaEx is an industrial research center for functional RNA delivery. The three academic partners are
For more information, contact:
Elin Esbjorner, Associate Professor,
+46 73 513 1431
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