Homo sapiens, Canis lupus familiaris, Mus musculus
Cell lines(s)
MDCK cell, HeLa cell
Protein name(s)
TFP1
Datatype
-
Molecular Function (MF)
-
Biological Process (BP)
cAMP-mediated signaling
Cellular Component (CC)
cAMP-dependent protein kinase complex
Biological Imaging Method
FRET, differences in fluorescence lifetime, time lapse microscopy
X scale
0.662 micrometer/pixel, 0.828 micrometer/pixel, 0.497 micrometer/pixel, 0.795 micrometer/pixel, NA
Y scale
0.662 micrometer/pixel, 0.828 micrometer/pixel, 0.497 micrometer/pixel, 0.795 micrometer/pixel, NA
Z scale
1 micrometer/pixel, NA, 2 micrometer/pixel
T scale
10.03 sec per time interval, 305 sec per time interval, 20 sec per time interval, 30 sec per time interval, 10.07 sec per time interval, 10.06 sec per time interval, 10.08 sec per time interval, NA
Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-
Related paper(s)
Tomoaki Kinjo, Tetsuya Watabe, Kenju Kobachi, Kenta Terai, Michiyuki Matsuda (2020) Single-Cell Activation of the cAMP-Signaling Pathway in 3D Tissues with FRET-Assisted Two-Photon Activation of bPAC., ACS chemical biology, Volume 15, Number 11, pp. 2848-2853
Published in 2020 Nov 20
(Electronic publication in Oct. 19, 2020, midnight )
(Abstract) Bacterial photoactivated adenylyl cyclase (bPAC) has been widely used in signal transduction research. However, due to its low two-photon absorption, bPAC cannot be efficiently activated by two-photon (2P) excitation. Taking advantage of the high two-photon absorption of monomeric teal fluorescent protein 1 (mTFP1), we herein developed 2P-activatable bPAC (2pabPAC), a fusion protein consisting of bPAC and mTFP1. In 2pabPAC, the energy absorbed by mTFP1 excites bPAC by Furster resonance energy transfer (FRET) at ca. 43% efficiency. The light-induced increase in cAMP was monitored by a red-shifted FRET biosensor for PKA. In 3D MDCK cells and mouse liver, PKA was activated at single-cell resolution under a 2P microscope. We found that PKA activation in a single hepatocyte caused PKA activation in neighboring cells, indicating the propagation of PKA activation. Thus, 2pabPAC will provide a versatile platform for controlling the cAMP signaling pathway and investigating cell-to-cell communication in vivo.