Tracking the Activity of mTORC1 in Living Cells Using Genetically Encoded FRET-based Biosensor TORCAR

摘要

Mechanistic target of rapamycin complex 1 (mTORC1) responds to multiple distinct signals (growth factors, amino acids, stress, energy level) and coordinates cell growth and proliferation. The activity of mTORC1 is exquisitely regulated in response to distinct stimuli, however, the underlying molecular mechanisms are still not fully understood. The spatial compartmentalization of mTORC1 signaling has been suggested to be an important mechanism for mTORC1 to achieve the signal specificity and efficiency. To examine the spatial regulation of the activity of mTORC1 in live cells, we describe a protocol using a newly developed molecular tool, a genetically encoded fluorescence resonance energy transfer (FRET)-based mTORC1 activity reporter, TORCAR. When expressed in the cell, TORCAR acts as a surrogate substrate of mTORC1, and exhibits a change in FRET in response to phosphorylation by mTORC1. Genetically targeting TORCAR to specific subcellular locations further allows for the characterization of spatial compartmentalized mTORC1 signaling.