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Protein Fibril-Based Intracellular Sono-Piezocatalysis via Nanoparticle-Enhanced Piezoelectricity
Soumi Das1, Reeddhi Ray1, Jayanta Dolai1
1School of Materials Science, Indian Association for the Cultivation of Science, 2A & 2B Raja S. C. Mullick Road, Kolkata 700032, India.
Researchers developed nanoparticle-conjugated lysozyme fibrils with enhanced piezoelectric properties for targeted cell therapy. These fibrils generate reactive oxygen species under ultrasound, inducing cancer cell death via oxidative stress.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Protein fibrils exhibit piezoelectricity, offering potential for mechanical stress-assisted cell therapy.
- Achieving stronger piezoelectric properties typically requires micron-length fibrils, which compromise colloidal properties and cellular targeting.
Purpose of the Study:
- To engineer colloidal lysozyme fibrils with enhanced piezoelectric properties for intracellular piezocatalysis.
- To improve cellular targeting and therapeutic efficacy using nanoparticle conjugation and functionalization.
Main Methods:
- Designed nanoparticle-conjugated lysozyme fibrils (300-400 nm length, 20 nm diameter).
- Functionalized fibrils with affinity molecules for selective cell targeting.
- Applied ultrasound to induce piezocatalysis and reactive oxygen species generation within cells.
Main Results:
- Achieved a moderate piezoelectric property of 29 pm/V in lysozyme fibrils.
- Enhanced piezoelectric property by 2 times and therapeutic potential by up to 10 times through nanoparticle conjugation.
- Demonstrated intracellular piezocatalysis leading to oxidative cell death and apoptosis.
Conclusions:
- Colloidal lysozyme fibrils with nanoparticle conjugation show significant potential for enhanced piezoelectric-based cell therapy.
- The developed system enables targeted delivery and ultrasound-triggered intracellular piezocatalysis for cancer treatment.
- Further exploration of piezoelectric protein fibrils in therapy is warranted.
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