Enzyme‐Directed and Organelle‐Specific Sphere‐to‐Fiber Nanotransformation Enhances Photodynamic Therapy in Cancer Cells

• Published in: Small methods Vol. 8; no. 11; pp. e2301551 - n/a
• Main Authors: Gan, Shenglong, Yang, Liu, Heng, Yiyuan, Chen, Qingxin, Wang, Dongqing, Zhang, Jie, Wei, Wenyu, Liu, Zhiyang, Njoku, Demian Ifeanyi, Chen, Jian Lin, Hu, Yi, Sun, Hongyan
• Format: Journal Article
• Language: English
• Published: Germany 01.11.2024
• Subjects: Alkaline Phosphatase - metabolism; Animals; Cell Line, Tumor; enzyme; Humans; Mitochondria - drug effects; Mitochondria - metabolism; Nanofibers - chemistry; Nanoparticles - chemistry; nanotransformation; Neoplasms - drug therapy; organelle; PDT; Photochemotherapy - methods; Photosensitizing Agents - chemistry; Photosensitizing Agents - pharmacology; Reactive Oxygen Species - metabolism; self‐assembly; Sirtuins - chemistry; Sirtuins - metabolism; enzyme; PDT; nanotransformation; organelle; self‐assembly
• DOI: 10.1002/smtd.202301551
• ISSN: 2366-9608

Employing responsive nanoplatforms as carriers for photosensitizers represents an effective strategy to overcome the challenges associated with photodynamic therapy (PDT), including poor solubility, low bioavailability, and high systemic toxicity. Drawing inspiration from the morphology transitions in biological systems, a general approach to enhance PDT that utilizes enzyme‐responsive nanoplatforms is developed. The transformation of phosphopeptide/photosensitizer co‐assembled nanoparticles is first demonstrated into nanofibers when exposed to cytoplasmic enzyme alkaline phosphatase. This transition is primarily driven by alkaline phosphatase‐induced changes of the nanoparticles in the hydrophilic and hydrophobic balance, and intermolecular electrostatic interactions within the nanoparticles. The resulting nanofibers exhibit improved ability of generating reactive oxygen species (ROS), intracellular accumulation, and retention in cancer cells. Furthermore, the enzyme‐responsive nanoplatform is expanded to selectively target mitochondria by mitochondria‐specific enzyme sirtuin 5 (SIRT5). Under the catalysis of SIRT5, the succinylated peptide/photosensitizer co‐assembled nanoparticles can be transformed into nanofibers specifically within the mitochondria. The resulting nanofibers exhibit excellent capability of modulating mitochondrial activity, enhanced ROS formation, and significant anticancer efficacy via PDT. Consequently, the enzyme‐instructed in situ fibrillar transformation of peptide/photosensitizers co‐assembled nanoparticles provides an efficient pathway to address the challenges associated with photosensitizers. It is envisaged that this approach will further expand the toolbox for enzyme‐responsive biomaterials for cancer therapy. A general approach utilizing enzyme‐responsive nanoplatforms to enhance photodynamic therapy is developed. When exposed to the cytoplasmic enzyme alkaline phosphatase or the mitochondrial enzyme sirtuin 5, the co‐assembled nanoparticles can be transformed into nanofibers in the cytoplasm or specifically within the mitochondria. The resulting nanofibers exhibit enhanced ROS formation and significant anticancer efficacy via photodynamic therapy.