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Competition Between Protein and DNA for Binding to Natural Sepiolite Nanofibers
David Adame Brooks1,2, Olivier Piétrement3, Elodie Dardillac1
1Université de Paris Cité, INSERM U1016, UMR 8104 CNRS, Institut Cochin, Paris, France.
International Journal of Nanomedicine
|March 10, 2025
Summary
Sepiolite nanofibers effectively bind DNA and proteins, crucial for nonviral gene transfer. Their adsorption is influenced by molecule charge and calcium ions, paving the way for nanoplatforms in clinical applications.
Area of Science:
- Materials Science
- Biotechnology
- Nanotechnology
Background:
- Sepiolite nanofibers, natural silicates, show potential as nanocarriers for biomolecule delivery.
- Their structure facilitates binding to various biomolecules like DNA and proteins through multiple interactions.
- Understanding competitive adsorption is key to optimizing nanocarrier function.
Purpose of the Study:
- To investigate the competitive adsorption of DNA and proteins onto sepiolite nanofibers.
- To elucidate the role of electrostatic interactions and calcium ions in the adsorption process.
- To assess the potential of sepiolite-based biohybrids for gene transfer applications.
Main Methods:
- Adsorption isotherms were used to measure protein binding efficiency (BSA and monoclonal antibody).
- Zeta potential measurements characterized surface charge properties.
- Competitive adsorption experiments analyzed the interplay between DNA and protein binding.
Main Results:
- Protein adsorption to sepiolite is charge-dependent and enhanced by CaCl2.
- Coating sepiolite with DNA reduced protein adsorption, an effect reversible by CaCl2.
- DNA binding efficiency decreased with protein pre-adsorption, with Ca2+ partially restoring it for BSA.
Conclusions:
- Electrostatic forces are primary drivers of protein adsorption onto sepiolite.
- Sepiolite-DNA and sepiolite-protein interactions are complex and influenced by ionic strength.
- Developed biohybrids offer a promising nanoplatform for gene delivery with potential clinical relevance.

