Open AccessSynthetic Artificial Apoptosis‐Inducing Receptor for On‐Demand Deactivation of Engineered Cells
Author(s) -
Monge Pere,
Løvschall Kaja Borup,
Søgaard Ane Bretschneider,
Walther Raoul,
Golbek Thaddeus W.,
Schmüser Lars,
Weidner Tobias,
Zelikin Alexander N.
Publication year - 2021
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202004432
Subject(s) - microbiology and biotechnology , receptor , chemistry , second messenger system , cell , signal transduction , population , biophysics , biology , biochemistry , demography , sociology
The design of a fully synthetic, chemical “apoptosis‐inducing receptor” (AIR) molecule is reported that is anchored into the lipid bilayer of cells, is activated by the incoming biological input, and responds with the release of a secondary messenger—a highly potent toxin for cell killing. The AIR molecule has four elements, namely, an exofacial trigger group, a bilayer anchor, a toxin as a secondary messenger, and a self‐immolative scaffold as a mechanism for signal transduction. Receptor installation into cells is established via a robust protocol with minimal cell handling. The synthetic receptor remains dormant in the engineered cells, but is effectively triggered externally by the addition of an activating biomolecule (enzyme) or in a mixed cell population through interaction with the surrounding cells. In 3D cell culture (spheroids), receptor activation is accessible for at least 5 days, which compares favorably with other state of the art receptor designs.