Hypoxia
in tumor tissues is the major obstacle to photodynamic
therapy (PDT). Herein, a self-oxygenating nanoplatform T4-Ce6-Cat
(T4CCa) is used for improving PDT. T4 acts as a nanocarrier, with
catalase (Cat) protein displayed on the capsid to trigger the hydrogen
peroxide (H2O2) degradation. The number of displayed
Cats can be precisely controlled by the feed concentration. Chemically
coupled chlorin e6 (Ce6) is a photosensitizer to generate reactive
oxygen species (ROS). By means of genetic engineering, phage display
technology, and chemical modification, the T4CCa converts to “super
tumor phage”. The 852 Cat molecules, displayed on the phage
surface, like a brush, increase the oxygen concentration to 21.7 mg/L
in a short time (1 min), which effectively relieves tumor hypoxia.
Adequate oxygen enables Ce6 to produce ROS effectively (93.6%), and
the tumor inhibition rate reaches 86.07%. In vitro and in vivo toxicity assays reveal that T4CCa exhibits
good biocompatibility at the molecular level, cellular level, and
tissue organ level. More importantly, Cat still has a high catalytic
capacity after T4CCa storage for a while. This work combines synthetic
biology and nanotechnology to alleviate tumor hypoxia, providing a
strategy for tumor treatment.