Author/Authors :
Lutz Kummer، نويسنده , , Chia-Wen Hsu، نويسنده , , Onur Dagliyan، نويسنده , , Christopher MacNevin، نويسنده , , Melanie Kaufholz، نويسنده , , Bastian Zimmermann، نويسنده , , Nikolay V. Dokholyan، نويسنده , , Klaus M. Hahn، نويسنده , , Andreas Plückthun، نويسنده ,
Abstract :
Investigation of protein activation in living cells is fundamental to understanding how proteins are influenced by the full complement of upstream regulators they experience. Here, we describe the generation of a biosensor based on the DARPin binding scaffold suited for intracellular applications. Combining library selection and knowledge-based design, we created an ERK activity biosensor by derivatizing a DARPin specific for phosphorylated ERK with a solvatochromatic merocyanine dye, whose fluorescence increases upon pERK binding. The biosensor specifically responded to pERK2, recognized by its conformation, but not to ERK2 or other closely related mitogen-activated kinases tested. Activated endogenous ERK was visualized in mouse embryo fibroblasts, revealing greater activation in the nucleus, perinuclear regions, and especially the nucleoli. The DARPin-based biosensor will serve as a useful tool for studying biological functions of ERK in vitro and in vivo.