Literature DB >> 3114258

Transducin interactions with rhodopsin. Evidence for positive cooperative behavior.

M Wessling-Resnick, G L Johnson.   

Abstract

Transducin and rhodopsin belong to a family of guanine nucleotide-binding (G) protein-coupled receptor systems that provide signal transduction mechanisms resulting in numerous metabolic responses in a variety of cell types. A simple, direct binding assay has been developed to investigate the molecular interactions between transducin and rhodopsin. The binding curves generated by these studies are sigmoidal, indicating an allosteric response. The Scatchard plots of this data display an asymptotic, bell-shaped character representative of the positive cooperative behavior. A Hill coefficient, nH = 1.92, was determined and found to be in close agreement with previous kinetic studies of allosterism described for rhodopsin's catalytic mechanism (Wessling-Resnick, M., and Johnson G.L. (1987) J. Biol. Chem. 262, 3697-3705). The value for Kd app was determined to be 0.05 microM. Bmax values obtained from the binding studies suggest that oligomeric complexes of rhodopsin may be involved in interactions with transducin to form multiple high affinity binding sites for the G protein. The positive cooperative behavior demonstrated in this investigation can provide insight into the molecular basis for regulation of other G protein-coupled receptor systems.

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Year:  1987        PMID: 3114258

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


  12 in total

Review 1.  Complexes between photoactivated rhodopsin and transducin: progress and questions.

Authors:  Beata Jastrzebska; Yaroslav Tsybovsky; Krzysztof Palczewski
Journal:  Biochem J       Date:  2010-04-28       Impact factor: 3.857

Review 2.  Oligomerization of G protein-coupled receptors: past, present, and future.

Authors:  Paul S-H Park; Slawomir Filipek; James W Wells; Krzysztof Palczewski
Journal:  Biochemistry       Date:  2004-12-21       Impact factor: 3.162

3.  A comparison of the efficiency of G protein activation by ligand-free and light-activated forms of rhodopsin.

Authors:  T J Melia; C W Cowan; J K Angleson; T G Wensel
Journal:  Biophys J       Date:  1997-12       Impact factor: 4.033

4.  Octyl glucoside extracts GTP-binding regulatory proteins from rat brain "synaptoneurosomes" as large, polydisperse structures devoid of beta gamma complexes and sensitive to disaggregation by guanine nucleotides.

Authors:  S Nakamura; M Rodbell
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

5.  2-Azido-[32P]NAD+, a photoactivatable probe for G-protein structure: evidence for holotransducin oligomers in which the ADP-ribosylated carboxyl terminus of alpha interacts with both alpha and gamma subunits.

Authors:  R R Vaillancourt; N Dhanasekaran; G L Johnson; A E Ruoho
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

6.  Rhodopsin-transducin heteropentamer: three-dimensional structure and biochemical characterization.

Authors:  Beata Jastrzebska; Philippe Ringler; David T Lodowski; Vera Moiseenkova-Bell; Marcin Golczak; Shirley A Müller; Krzysztof Palczewski; Andreas Engel
Journal:  J Struct Biol       Date:  2011-09-06       Impact factor: 2.867

7.  The gamma subunit of transducin is farnesylated.

Authors:  R K Lai; D Perez-Sala; F J Cañada; R R Rando
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

8.  Quaternary structures of opsin in live cells revealed by FRET spectrometry.

Authors:  Ashish K Mishra; Megan Gragg; Michael R Stoneman; Gabriel Biener; Julie A Oliver; Przemyslaw Miszta; Slawomir Filipek; Valerică Raicu; Paul S-H Park
Journal:  Biochem J       Date:  2016-09-13       Impact factor: 3.857

9.  The photoactivatable NAD+ analogue [32P]2-azido-NAD+ defines intra- and inter-molecular interactions of the C-terminal domain of the G-protein G alpha t.

Authors:  R R Vaillancourt; N Dhanasekaran; A E Ruoho
Journal:  Biochem J       Date:  1995-11-01       Impact factor: 3.857

10.  Functional assays of membrane-bound proteins with SAMDI-TOF mass spectrometry.

Authors:  Violeta L Marin; Timothy H Bayburt; Stephen G Sligar; Milan Mrksich
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

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