Downloads: 299

Files in This Item:
File Description SizeFormat 
mbc.E11-01-0072.pdf1.07 MBAdobe PDFView/Open
Title: Development of an optimized backbone of FRET biosensors for kinases and GTPases.
Authors: Komatsu, Naoki
Aoki, Kazuhiro  KAKEN_id
Yamada, Masashi
Yukinaga, Hiroko
Fujita, Yoshihisa  kyouindb  KAKEN_id
Kamioka, Yuji  KAKEN_id
Matsuda, Michiyuki  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-5876-9969 (unconfirmed)
Author's alias: 青木, 一洋
Issue Date: Dec-2011
Publisher: American Society for Cell Biology
Journal title: Molecular biology of the cell
Volume: 22
Issue: 23
Start page: 4647
End page: 4656
Abstract: Biosensors based on the principle of Förster (or fluorescence) resonance energy transfer (FRET) have shed new light on the spatiotemporal dynamics of signaling molecules. Among them, intramolecular FRET biosensors have been increasingly used due to their high sensitivity and user-friendliness. Time-consuming optimizations by trial and error, however, obstructed the development of intramolecular FRET biosensors. Here we report an optimized backbone for rapid development of highly sensitive intramolecular FRET biosensors. The key concept is to exclude the "orientation-dependent" FRET and to render the biosensors completely "distance-dependent" with a long, flexible linker. We optimized a pair of fluorescent proteins for distance-dependent biosensors, and then developed a long, flexible linker ranging from 116 to 244 amino acids in length, which reduced the basal FRET signal and thereby increased the gain of the FRET biosensors. Computational simulations provided insight into the mechanisms by which this optimized system was the rational strategy for intramolecular FRET biosensors. With this backbone system, we improved previously reported FRET biosensors of PKA, ERK, JNK, EGFR/Abl, Ras, and Rac1. Furthermore, this backbone enabled us to develop novel FRET biosensors for several kinases of RSK, S6K, Akt, and PKC and to perform quantitative evaluation of kinase inhibitors in living cells.
Rights: © 2011 by The American Society for Cell Biology.
URI: http://hdl.handle.net/2433/151847
DOI(Published Version): 10.1091/mbc.E11-01-0072
PubMed ID: 21976697
Appears in Collections:Journal Articles

Show full item record

Export to RefWorks


Export Format: 


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.