Because protein drugs are unstable in the body, they must be given at high levels, which can cause side effects. Scientists have tried to protect protein therapies from degradation by encapsulating them in carriers, such as liposomes, nanoparticles and RBCs. But it has been challenging to make the carriers release their cargo at the appropriate place and time. Brianna Vickerman, David Lawrence and colleagues wanted to engineer RBCs to release therapeutic proteins at specific regions of the body when triggered by certain wavelengths of light.

The researchers embedded a peptide, called melittin, into the cell membrane of RBCs. A component of European honey bee venom, melittin normally causes RBCs to rupture. But the team modified the peptide so that it would do so only when illuminated by a specific wavelength of light. As a proof of concept, the researchers loaded thrombin -- a blood-clotting enzyme that is used to prevent excessive bleeding -- into the engineered RBCs and injected them into mice. They then shone a light on a small region of each mouse's ear and examined sections of the tissue. The analysis showed thrombin-related blood clotting only at the illuminated sites. The strategy could prove useful for the light-triggered release of protein, peptide and nucleic acid therapeutics from a variety of lipid-based carriers, the researchers say.

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Journal Reference:

1. Brianna M. Vickerman, Colin P. O’Banion, Xianming Tan, David. S. Lawrence. Light-Controlled Release of Therapeutic Proteins from Red Blood Cells. ACS Central Science, 2020; DOI: 10.1021/acscentsci.0c01151