Rho MultiBinder, a fluorescent biosensor that reports the activity of multiple GTPases

• Published in: Biophysical journal Vol. 122; no. 18; pp. 3646 - 3655
• Main Authors: Pimenta, Frederico M., Huh, Jaewon, Guzman, Bryan, Amanah, Diepreye, Marston, Daniel J., Pinkin, Nicholas K., Danuser, Gaudenz, Hahn, Klaus M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 19.09.2023; The Biophysical Society
• Subjects: Biosensing Techniques - methods; cdc42 GTP-Binding Protein - metabolism; Cell Surface Extensions; Coloring Agents; Fluorescence Resonance Energy Transfer - methods; rac1 GTP-Binding Protein - metabolism; rho GTP-Binding Proteins - metabolism; rhoA GTP-Binding Protein - metabolism; Signal Transduction
• ISSN: 0006-3495; 1542-0086; 1542-0086
• DOI: 10.1016/j.bpj.2023.04.020

Imaging two or more fluorescent biosensors in the same living cell can reveal the spatiotemporal coordination of protein activities. However, using multiple Förster resonance energy transfer (FRET) biosensors together is challenging due to toxicity and the need for orthogonal fluorophores. Here we generate a biosensor component that binds selectively to the activated conformation of three different proteins. This enabled multiplexed FRET with fewer fluorophores, and reduced toxicity. We generated this MultiBinder (MB) reagent for the GTPases RhoA, Rac1, and Cdc42 by combining portions of the downstream effector proteins Pak1 and Rhotekin. Using FRET between mCherry on the MB and YPet or mAmetrine on two target proteins, the activities of any pair of GTPases could be distinguished. The MB was used to image Rac1 and RhoA together with a third, dye-based biosensor for Cdc42. Quantifying effects of biosensor combinations on the frequency, duration, and velocity of cell protrusions and retractions demonstrated reduced toxicity. Multiplexed imaging revealed signaling hierarchies between the three proteins at the cell edge where they regulate motility.