Unveiling Sticholysin II and plasmid DNA interaction: Implications for developing non-viral vectors

• Published in: Toxicon (Oxford) Vol. 238; p. 107571
• Main Authors: Escalona-Rodriguez, Felipe A, Cruz-Leal, Yoelys, La O-Bonet, Javier, Pérez-Erviti, Julio A, Valdés-Tresanco, Mario Ernesto, Rivero-Hernández, Ada L, Sifontes-Niebla, Maricary, Manso-Vargas, Alexis, Sánchez, Belinda, Alvarez, Carlos, Barbosa, Leandro R S, Itri, Rosangela, Lanio, María E
• Format: Journal Article
• Language: English
• Published: England 01-02-2024
• Subjects: Non-viral delivery system; Sticholysins; Plasmid DNA; Pore-forming proteins
• ISSN: 0041-0101; 1879-3150
• DOI: 10.1016/j.toxicon.2023.107571

Non-viral gene delivery systems offer significant potential for gene therapy due to their versatility, safety, and cost advantages over viral vectors. However, their effectiveness can be hindered by the challenge of efficiently releasing the genetic cargo from endosomes to prevent degradation in lysosomes. To overcome this obstacle, functional components can be incorporated into these systems. Sticholysin II (StII) is one of the pore-forming proteins derived from the sea anemone Stichodactyla helianthus, known for its high ability to permeabilize cellular and model membranes. In this study, we aimed to investigate the interaction between StII, and a model plasmid (pDNA) as an initial step towards designing an improved vector with enhanced endosomal escape capability. The electrophoretic mobility shift assay (EMSA) confirmed the formation of complexes between StII and pDNA. Computational predictions identified specific residues involved in the StII-DNA interaction interface, highlighting the importance of electrostatic interactions and hydrogen bonds in mediating the binding. Atomic force microscopy (AFM) of StII-pDNA complexes revealed the presence of nodular fiber and toroid shapes. These complexes were found to have a predominantly micrometer size, as confirmed by dynamic light scattering (DLS) measurements. Despite increase in the overall charge, the complexes formed at the evaluated nitrogen-to-phosphorus (N/P) ratios still maintained a negative charge. Moreover, StII retained its pore-forming capacity regardless of its binding to the complexes. These findings suggest that the potential ability of StII to permeabilize endosomal membranes could be largely maintained when combined with nucleic acid delivery systems. Additionally, the still remaining negative charge of the complexes would enable the association of another positively charged component to compact pDNA. However, to minimize non-specific cytotoxic effects, it is advisable to explore methods to regulate the protein's activity in response to the microenvironment.