| First Author | Maziarz M | Year | 2020 |
| Journal | Cell | Volume | 182 |
| Issue | 3 | Pages | 770-785.e16 |
| PubMed ID | 32634377 | Mgi Jnum | J:379774 |
| Mgi Id | MGI:7865921 | Doi | 10.1016/j.cell.2020.06.020 |
| Citation | Maziarz M, et al. (2020) Revealing the Activity of Trimeric G-proteins in Live Cells with a Versatile Biosensor Design. Cell 182(3):770-785.e16 |
| abstractText | Heterotrimeric G-proteins (Galphabetagamma) are the main transducers of signals from GPCRs, mediating the action of countless natural stimuli and therapeutic agents. However, there are currently no robust approaches to directly measure the activity of endogenous G-proteins in cells. Here, we describe a suite of optical biosensors that detect endogenous active G-proteins with sub-second resolution in live cells. Using a modular design principle, we developed genetically encoded, unimolecular biosensors for endogenous Galpha-GTP and free Gbetagamma: the two active species of heterotrimeric G-proteins. This design was leveraged to generate biosensors with specificity for different heterotrimeric G-proteins or for other G-proteins, such as Rho GTPases. Versatility was further validated by implementing the biosensors in multiple contexts, from characterizing cancer-associated G-protein mutants to neurotransmitter signaling in primary neurons. Overall, the versatile biosensor design introduced here enables studying the activity of endogenous G-proteins in live cells with high fidelity, temporal resolution, and convenience. |
