Single-color, ratiometric biosensors for detecting signaling activities in live cells

Brian Ross(Johns Hopkins University), Brian Tenner(Johns Hopkins University), Michele L. Markwardt(University of Maryland, Baltimore), Adam Zviman(University of Maryland, Baltimore), Guoli Shi(University of Maryland, Baltimore), Jaclyn P. Kerr(University of Maryland, Baltimore), Nicole E. Snell(University of Maryland, Baltimore), Jennifer J McFarland(University of Maryland, Baltimore), Joseph R. H. Mauban(University of Maryland, Baltimore), Christopher W. Ward(University of Maryland, Baltimore), Megan A. Rizzo(University of Maryland, Baltimore), Jin Zhang(Johns Hopkins University)
eLife
July 2, 2018
Cited by 85Open Access
Full Text

Abstract

Genetically encoded fluorescent biosensors have revolutionized the study of signal transduction by enabling the real-time tracking of signaling activities in live cells. Investigating the interaction between signaling networks has become increasingly important to understanding complex cellular phenomena, necessitating an update of the biosensor toolkit to allow monitoring and perturbing multiple activities simultaneously in the same cell. We therefore developed a new class of fluorescent biosensors based on homo-FRET, deemed FLuorescence Anisotropy REporters (FLAREs), which combine the multiplexing ability of single-color sensors with a quantitative, ratiometric readout. Using an array of color variants, we were able to demonstrate multiplexed imaging of three activity reporters simultaneously in the same cell. We further demonstrate the compatibility of FLAREs for use with optogenetic tools as well as intravital two-photon imaging.


Related Papers

No related papers found

Powered by citation graph analysis