Staff member

Roger Riera Brillas

PhD Student
Nanoscopy for Nanomedicine
+34 934 020 514
Staff member publications

Abasolo, Ibane, Seras-Franzoso, Joaquin, Díaz-Riascos, Zamira Vanessa, Corchero, José Luis, González, Patricia, García-Aranda, Natalia, Mandaña, Monica, Riera, Roger, Boullosa, Ana, Mancilla, Sandra, Grayston, Alba, Moltó-Abad, Marc, Garcia-Fruitós, Elena, Mendoza, Rosa, Pintos-Morell, Guillem, Albertazzi, Lorenzo, Rosell, Anna, Casas, Josefina, Villaverde, Antonio, Schwartz, Simó, (2020). Extracellular vesicles increase the enzymatic activity of lysosomal proteins and improve the efficacy of enzyme replacement therapy in Fabry disease Molecular Genetics and Metabolism 16th Annual Research Meeting of the WORLDSymposium , Elsevier (Orlando, USA) 129, (2), S16

Riera, R., Feiner-Gracia, N., Fornaguera, C., Cascante, A., Borrós, S., Albertazzi, L., (2019). Tracking the DNA complexation state of pBAE polyplexes in cells with super resolution microscopy Nanoscale 11, (38), 17869-17877

The future of gene therapy relies on the development of efficient and safe delivery vectors. Poly(β-amino ester)s are promising cationic polymers capable of condensing oligonucleotides into nanoparticles – polyplexes – and deliver them into the cell nucleus, where the gene material would be expressed. The complexation state during the crossing of biological barriers is crucial: polymers should tightly complex DNA before internalization and then release to allow free DNA to reach the nucleus. However, measuring the complexation state in cells is challenging due to the nanometric size of polyplexes and the difficulties to study the two components (polymer and DNA) independently. Here we propose a method to visualize and quantify the two components of a polyplex inside cells, with nanometre scale resolution, using two-colour direct stochastic reconstruction super-resolution microscopy (dSTORM). With our approach, we tracked the complexation state of pBAE polyplexes from cell binding to DNA release and nuclear entry revealing time evolution and the final fate of DNA and pBAE polymers in mammalian cells.