Literature DB >> 16757347

Analyses of Rem/RGK signaling and biological activity.

Douglas A Andres1, Shawn M Crump, Robert N Correll, Jonathan Satin, Brian S Finlin.   

Abstract

Rem (Rad and Gem related) is a member of the RGK family of Ras-related GTPases that also includes Rad, Rem2, and Gem/Kir. All RGK proteins share structural features that are distinct from other Ras-related proteins, including several nonconservative amino acid substitutions within regions known to participate in nucleotide binding and hydrolysis and a C-terminal extension that contains regulatory sites that seem to control both subcellular location and function. Rem is known to modulate two distinct signal transduction pathways, regulating both cytoskeletal reorganization and voltage-gated Ca2+ channel activity. In this chapter, we summarize the experimental approaches used to characterize the interaction of Rem with 14-3-3 proteins and Ca2+ channel beta-subunits and describe electrophysiological analyses for characterizing Rem-mediated regulation of L-type Ca2+ channel activity.

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Year:  2006        PMID: 16757347     DOI: 10.1016/S0076-6879(05)07039-4

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  5 in total

1.  Rem GTPase interacts with the proximal CaV1.2 C-terminus and modulates calcium-dependent channel inactivation.

Authors:  Chunyan Pang; Shawn M Crump; Ling Jin; Robert N Correll; Brian S Finlin; Jonathan Satin; Douglas A Andres
Journal:  Channels (Austin)       Date:  2010-05-01       Impact factor: 2.581

Review 2.  The RGK family of GTP-binding proteins: regulators of voltage-dependent calcium channels and cytoskeleton remodeling.

Authors:  Robert N Correll; Chunyan Pang; Dana M Niedowicz; Brian S Finlin; Douglas A Andres
Journal:  Cell Signal       Date:  2007-11-06       Impact factor: 4.315

3.  Plasma membrane targeting is essential for Rem-mediated Ca2+ channel inhibition.

Authors:  Robert N Correll; Chunyan Pang; Brian S Finlin; Alexandria M Dailey; Jonathan Satin; Douglas A Andres
Journal:  J Biol Chem       Date:  2007-08-07       Impact factor: 5.157

4.  Analysis of the Rem2 - voltage dependant calcium channel beta subunit interaction and Rem2 interaction with phosphorylated phosphatidylinositide lipids.

Authors:  Robert N Correll; Gregory J Botzet; Jonathan Satin; Douglas A Andres; Brian S Finlin
Journal:  Cell Signal       Date:  2007-11-06       Impact factor: 4.315

5.  Calmodulin binding is dispensable for Rem-mediated Ca2+ channel inhibition.

Authors:  Robert N Correll; Chunyan Pang; Dana M Niedowicz; Jonathan Satin; Douglas A Andres
Journal:  Mol Cell Biochem       Date:  2007-12-04       Impact factor: 3.396

  5 in total

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