Technology ID

Removal of Selected Proteins Using Light Energy: Photoimmunotherapy

Lead Inventor
Kobayashi, Hisataka (NCI)
Schnermann, Martin (NCI)
Choyke, Peter (NCI)
Research Materials
Therapeutic Areas
Development Stages
Lead IC

Researchers at the NCI  Laboratory of Molecular Theranostics and the Molecular Imaging Program have developed a new method to modify, isolate and remove a single chemically-labeled molecule or a cluster of proteins associated with the chemically-labeled protein. The chemical label can be an antigen-antibody complex. This discovery is based on the mechanism of photo-immunotherapy (PIT). Unlike PIT, however, which is used for direct therapy, the above-identified technology can be used for controlled drug delivery (e.g., removing unbound drug moieties from circulation) and active detoxification of potentially poisonous material (e.g. bacteria, toxins, virus, venom etc.).

The current state of the art does not readily allow for simple labeling and isolation of proteins or other biomolecules from complex tissue samples or bodily fluids. The technology consists of using a conjugate of the dye IR700 and a biomolecule with specific binding activity, such as an antibody, to label the cell type or target molecule of interest, followed by irradiation of the sample with light in the near IR spectrum.  Upon exposure, the IR700 moiety becomes hydrophobic and aggregates, allowing for mechanical separation of the target molecule or cell type of interest as a complex with the IR700 conjugate. Labeling of cancerous cells in vivo with IR700 conjugates, followed by irradiation in the near IR spectrum, causes cell death.

Competitive Advantages:

Simple and versatile way to separate and remove molecules or cells from a complex mixture.

Commercial Applications:

- In vivo removal of toxins, pathogens or drugs from a subject
- Cancer imunotherapy

Licensing Contact:
Clouse, Thomas