Literature DB >> 16418172

Dynamics of the Ras/ERK MAPK cascade as monitored by fluorescent probes.

Aki Fujioka1, Kenta Terai, Reina E Itoh, Kazuhiro Aoki, Takeshi Nakamura, Shinya Kuroda, Eisuke Nishida, Michiyuki Matsuda.   

Abstract

To comprehend the Ras/ERK MAPK cascade, which comprises Ras, Raf, MEK, and ERK, several kinetic simulation models have been developed. However, a large number of parameters that are essential for the development of these models are still missing and need to be set arbitrarily. Here, we aimed at collecting these missing parameters using fluorescent probes. First, the levels of the signaling molecules were quantitated. Second, to monitor both the activation and nuclear translocation of ERK, we developed probes based on the principle of fluorescence resonance energy transfer. Third, the dissociation constants of Ras.Raf, Raf.MEK, and MEK.ERK complexes were estimated using a fluorescent tag that can be highlighted very rapidly. Finally, the same fluorescent tag was used to measure the nucleocytoplasmic shuttling rates of ERK and MEK. Using these parameters, we developed a kinetic simulation model consisting of the minimum essential members of the Ras/ERK MAPK cascade. This simple model reproduced essential features of the observed activation and nuclear translocation of ERK. In this model, the concentration of Raf significantly affected the levels of phospho-MEK and phospho-ERK upon stimulation. This prediction was confirmed experimentally by decreasing the level of Raf using the small interfering RNA technique. This observation verified the usefulness of the parameters collected in this study.

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Year:  2006        PMID: 16418172     DOI: 10.1074/jbc.M509344200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  140 in total

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2.  Obtaining and estimating kinetic parameters from the literature.

Authors:  Susana R Neves
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Review 3.  Visualizing dynamic activities of signaling enzymes using genetically encodable FRET-based biosensors from designs to applications.

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Journal:  Methods Enzymol       Date:  2012       Impact factor: 1.600

4.  Multiple decisive phosphorylation sites for the negative feedback regulation of SOS1 via ERK.

Authors:  Yuji Kamioka; Shuhei Yasuda; Yoshihisa Fujita; Kazuhiro Aoki; Michiyuki Matsuda
Journal:  J Biol Chem       Date:  2010-08-19       Impact factor: 5.157

5.  1.8 A bright-state structure of the reversibly switchable fluorescent protein Dronpa guides the generation of fast switching variants.

Authors:  Andre C Stiel; Simon Trowitzsch; Gert Weber; Martin Andresen; Christian Eggeling; Stefan W Hell; Stefan Jakobs; Markus C Wahl
Journal:  Biochem J       Date:  2007-02-15       Impact factor: 3.857

6.  Quantitative analysis of ERK2 interactions with substrate proteins: roles for kinase docking domains and activity in determining binding affinity.

Authors:  Kimberly A Burkhard; Fengming Chen; Paul Shapiro
Journal:  J Biol Chem       Date:  2010-11-22       Impact factor: 5.157

7.  Structural basis for reversible photoswitching in Dronpa.

Authors:  Martin Andresen; Andre C Stiel; Simon Trowitzsch; Gert Weber; Christian Eggeling; Markus C Wahl; Stefan W Hell; Stefan Jakobs
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-23       Impact factor: 11.205

Review 8.  FRET and mechanobiology.

Authors:  Yingxiao Wang; Ning Wang
Journal:  Integr Biol (Camb)       Date:  2009-10       Impact factor: 2.192

9.  The Xenopus oocyte: a single-cell model for studying Ca2+ signaling.

Authors:  Yaping Lin-Moshier; Jonathan S Marchant
Journal:  Cold Spring Harb Protoc       Date:  2013-03-01

10.  The scaffold protein Shoc2/SUR-8 accelerates the interaction of Ras and Raf.

Authors:  Rie Matsunaga-Udagawa; Yoshihisa Fujita; Sayaka Yoshiki; Kenta Terai; Yuji Kamioka; Etsuko Kiyokawa; Katsuyuki Yugi; Kazuhiro Aoki; Michiyuki Matsuda
Journal:  J Biol Chem       Date:  2010-01-05       Impact factor: 5.157

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