posted on 2016-02-10, 15:48authored bySung Bae Kim, Ryo Nishihara, Daniel Citterio, Koji Suzuki
Optical imaging of protein–protein
interactions (PPIs) facilitates
comprehensive elucidation of intracellular molecular events. We demonstrate
an optical measure for visualizing molecular tension triggered by
any PPI in mammalian cells. Twenty-three kinds of candidate designs
were fabricated, in which a full-length artificial luciferase (ALuc)
was sandwiched between two model proteins of interest, e.g., FKBP
and FRB. One of the designs greatly enhanced the bioluminescence in
response to varying concentrations of rapamycin. It is confirmed with
negative controls that the elevated bioluminescence is solely motivated
from the molecular tension. The probe design was further modified
toward eliminating the C-terminal end of ALuc and was found to improve
signal-to-background ratios, named “a combinational probe”.
The utilities were elucidated with detailed substrate selectivity,
bioluminescence imaging of live cells, and different PPI models. This
study expands capabilities of luciferases as a tool for analyses of
molecular dynamics and cell signaling in living subjects.