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Published February 11, 2016 | Supplemental Material + Accepted Version
Journal Article Open

Engineering Customized Cell Sensing and Response Behaviors Using Synthetic Notch Receptors

Abstract

The Notch protein is one of the most mechanistically direct transmembrane receptors—the intracellular domain contains a transcriptional regulator that is released from the membrane when engagement of the cognate extracellular ligand induces intramembrane proteolysis. We find that chimeric forms of Notch, in which both the extracellular sensor module and the intracellular transcriptional module are replaced with heterologous protein domains, can serve as a general platform for generating novel cell-cell contact signaling pathways. Synthetic Notch (synNotch) pathways can drive user-defined functional responses in diverse mammalian cell types. Because individual synNotch pathways do not share common signaling intermediates, the pathways are functionally orthogonal. Thus, multiple synNotch receptors can be used in the same cell to achieve combinatorial integration of environmental cues, including Boolean response programs, multi-cellular signaling cascades, and self-organized cellular patterns. SynNotch receptors provide extraordinary flexibility in engineering cells with customized sensing/response behaviors to user-specified extracellular cues.

Additional Information

© 2016 Elsevier Inc. Received: November 27, 2015. Revised: January 4, 2016. Accepted: January 8, 2016. Published: January 28, 2016. We would like to thank members of the Lim lab for helpful discussions and comments on the manuscript. We thank K. McNally and Joan Garbarino for technical assistance and R. Nicoll for neurons. This work was supported by a Jane Coffin Childs Memorial Fund Postdoctoral Fellowship A121505 (K.T.R.), a Human Frontiers of Science Program (HFSP), a European Molecular Biology Organization (EMBO) Postdoctoral Fellowship (L.M.), NIH grants K99 1K99EB021030 (L.M.), PN2 EY016546, P50GM081879, R01 GM055040, and R01 CA196277, and the Howard Hughes Medical Institute (W.A.L.).

Attached Files

Accepted Version - nihms751441.pdf

Supplemental Material - mmc1.xlsx

Supplemental Material - mmc2.mp4

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