4.6 Article

Targeting and photodynamic killing of a microbial pathogen using protein cage Architectures functionalized with a photosensitizer

Journal

LANGMUIR
Volume 23, Issue 24, Pages 12280-12286

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la7021424

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The selectivity of antimicrobial photodynamic therapy (PDT) can be enhanced by coupling the photosensitizer (PS) to a targeting ligand. Nanoplatforms provide a medium for designing delivery vehicles that incorporate both functional attributes. We report here the photodynamic inactivation of a pathogenic bacterium, Stapkylococcus aureus, using targeted nanoplatforms conjugated to a photosensitizer (PS). Both electrostatic and complementary biological interactions were used to mediate targeting. Genetic constructs of a protein cage architecture allowed site-specific chemical functionalization with the PS and facilitated dual functionalization with the PS and the targeting ligand. These results demonstrate that protein cage architectures can serve as versatile templates for engineering nanoplatforms for targeted antimicrobial PDT.

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