Peptide Amphiphiles and Gene Therapy: Why Amorphous Nanostructures Outperform Fibrils
A New Twist in Viral Gene Delivery Gene therapy holds the promise of treating diseases at their source by rewriting faulty genetic instructions. Central to this approach are retroviral vectors—viruses repurposed to deliver therapeutic genes into human cells. Despite their potential, one major hurdle remains: getting these vectors to efficiently attach and enter target cells. […]
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