Green‐Light‐Activated Photoreaction via Genetic Hybridization of Far‐Red Fluorescent Protein and Silk
Source abstract
Abstract
Abstract Fluorescent proteins often result in phototoxicity and cytotoxicity, in particular because some red fluorescent proteins produce and release reactive oxygen species (ROS). The photogeneration of ROS is considered as a detrimental side effect in cellular imaging or is proactively utilized for ablating cancerous tissue. As ancient textiles or biomaterials, silk produced by silkworms can directly be used as fabrics or be processed into materials and structures to host other functional nanomaterials. It is reported that transgenic fusion of far‐red fluorescent protein (mKate2) with silk provides a photosensitizer hybridization platform for photoinducible control of ROS. Taking advantage of green (visible) light activation, native and regenerated mKate2 silk can produce and release superoxide and singlet oxygen, in a comparable manner of visible light‐driven plasmonic photocatalysis. Thus, the genetic expression of mKate2 in silk offers immediately exploitable and scalable photocatalyst‐like biomaterials. It is further envisioned that mKate2 silk can potentially rule out hazardous concerns associated with foreign semiconductor photocatalytic nanomaterials.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Silk-based biomaterials and applications · Nanoplatforms for cancer theranostics · Cancer Research and Treatments
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Weldon School of Biomedical Engineering Purdue University West Lafayette IN 47907 USA
Department of Agricultural Biology National Institute of Agricultural Sciences Rural Development Administration Wanju Jeollabuk‐do 55365 Republic of Korea
Regenstrief Center for Healthcare Engineering Purdue University West Lafayette IN 47907 USA
Purdue Quantum Center Purdue University West Lafayette IN 47907 USA
Funding
Air Force Office of Scientific Research
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