The Journal of General Physiology
Cell MicroControls
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Full Text (PDF, 2535K)
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JGP
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dumke, C. L.
Right arrow Articles by Pugh, E. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dumke, C. L.
Right arrow Articles by Pugh, E. N., Jr
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

The Journal of General Physiology, Vol 103, 1071-1098, Copyright © 1994 by The Rockefeller University Press


ARTICLES

Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase

CL Dumke, VY Arshavsky, PD Calvert, MD Bownds and EN Pugh Jr
Bock Laboratories, University of Wisconsin, Madison 53706.

Cyclic GMP hydrolysis by the phosphodiesterase (PDE) of retinal rod outer segments (ROS) is a key amplification step in phototransduction. Definitive estimates of the turnover number, kcat, and of the Km are crucial to quantifying the amplification contributed by the PDE. Published estimates for these kinetic parameters vary widely; moreover, light-dependent changes in the Km of PDE have been reported. The experiments and analyses reported here account for most observed variations in apparent Km, and they lead to definitive estimates of the intrinsic kinetic parameters in amphibian rods. We first obtained a new and highly accurate estimate of the ratio of holo-PDE to rhodopsin in the amphibian ROS, 1:270. We then estimated the apparent kinetic parameters of light-activated PDE of suspensions of disrupted frog ROS whose structural integrity was systematically varied. In the most severely disrupted ROS preparation, we found Km = 95 microM and kcat = 4,400 cGMP.s-1. In suspensions of disc-stack fragments of greater integrity, the apparent Km increased to approximately 600 microM, though kcat remained unchanged. In contrast, the Km for cAMP was not shifted in the disc stack preparations. A theoretical analysis shows that the elevated apparent Km of suspensions of disc stacks can be explained as a consequence of diffusion with hydrolysis in the disc stack, which causes active PDEs nearer the center of the stack to be exposed to a lower concentration of cyclic GMP than PDEs at the disc stack rim. The analysis predicts our observation that the apparent Km for cGMP is elevated with no accompanying decrease in kcat. The analysis also predicts the lack of a Km shift for cAMP and the previously reported light dependence of the apparent Km for cGMP. We conclude that the intrinsic kinetic parameters of the PDE do not vary with light or structural integrity, and are those of the most severely disrupted disc stacks.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
Q. Wang, X. Zhang, L. Zhang, F. He, G. Zhang, M. Jamrich, and T. G. Wensel
Activation-dependent Hindrance of Photoreceptor G Protein Diffusion by Lipid Microdomains
J. Biol. Chem., October 31, 2008; 283(44): 30015 - 30024.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
G. Caruso, P. Bisegna, L. Shen, D. Andreucci, H. E. Hamm, and E. DiBenedetto
Modeling the Role of Incisures in Vertebrate Phototransduction
Biophys. J., August 15, 2006; 91(4): 1192 - 1212.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. C. Pentia, S. Hosier, and R. H. Cote
The Glutamic Acid-rich Protein-2 (GARP2) Is a High Affinity Rod Photoreceptor Phosphodiesterase (PDE6)-binding Protein That Modulates Its Catalytic Properties
J. Biol. Chem., March 3, 2006; 281(9): 5500 - 5505.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
X. Zhang, Q. Feng, and R. H. Cote
Efficacy and Selectivity of Phosphodiesterase-Targeted Drugs in Inhibiting Photoreceptor Phosphodiesterase (PDE6) in Retinal Photoreceptors
Invest. Ophthalmol. Vis. Sci., September 1, 2005; 46(9): 3060 - 3066.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
D. Holcman and J. I. Korenbrot
The Limit of Photoreceptor Sensitivity: Molecular Mechanisms of Dark Noise in Retinal Cones
J. Gen. Physiol., May 31, 2005; 125(6): 641 - 660.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
S. Ramanathan, P. B. Detwiler, A. M. Sengupta, and B. I. Shraiman
G-Protein-Coupled Enzyme Cascades Have Intrinsic Properties that Improve Signal Localization and Fidelity
Biophys. J., May 1, 2005; 88(5): 3063 - 3071.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
D. Andreucci, P. Bisegna, G. Caruso, H.E. Hamm, and E. DiBenedetto
Mathematical Model of the Spatio-Temporal Dynamics of Second Messengers in Visual Transduction
Biophys. J., September 1, 2003; 85(3): 1358 - 1376.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
M. R. D'Amours, A. E. Granovsky, N. O. Artemyev, and R. H. Cote
Potency and Mechanism of Action of E4021, a Type 5 Phosphodiesterase Isozyme-Selective Inhibitor, on the Photoreceptor Phosphodiesterase Depend on the State of Activation of the Enzyme
Mol. Pharmacol., March 1, 1999; 55(3): 508 - 514.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
M. C. Hebert, F. Schwede, B. Jastorff, and R. H. Cote
Structural Features of the Noncatalytic cGMP Binding Sites of Frog Photoreceptor Phosphodiesterase Using cGMP Analogs
J. Biol. Chem., March 6, 1998; 273(10): 5557 - 5565.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. K. Florio, R. K. Prusti, and J. A. Beavo
Solubilization of Membrane-bound Rod Phosphodiesterase by the Rod Phosphodiesterase Recombinant delta Subunit
J. Biol. Chem., September 27, 1996; 271(39): 24036 - 24047.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
V. A. Klenchin, P. D. Calvert, and M. D. Bownds
Inhibition of Rhodopsin Kinase by Recoverin
J. Biol. Chem., July 7, 1995; 270(27): 16147 - 16152.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. W. Norton, M. R. D'Amours, H. J. Grazio, T. L. Hebert, and R. H. Cote
Mechanism of Transducin Activation of Frog Rod Photoreceptor Phosphodiesterase. ALLOSTERIC INTERACTIONS BETWEEN THE INHIBITORY gamma SUBUNIT AND THE NONCATALYTIC cGMP-BINDING SITES
J. Biol. Chem., December 1, 2000; 275(49): 38611 - 38619.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. E. Granovsky and N. O. Artemyev
Partial Reconstitution of Photoreceptor cGMP Phosphodiesterase Characteristics in cGMP Phosphodiesterase-5
J. Biol. Chem., June 8, 2001; 276(24): 21698 - 21703.
[Abstract] [Full Text] [PDF]



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents