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

Publication ,  Journal Article
Dumke, CL; Arshavsky, VY; Calvert, PD; Bownds, MD; Pugh, EN
Published in: J Gen Physiol
June 1994

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.

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Published In

J Gen Physiol

DOI

ISSN

0022-1295

Publication Date

June 1994

Volume

103

Issue

6

Start / End Page

1071 / 1098

Location

United States

Related Subject Headings

  • Rod Cell Outer Segment
  • Rhodopsin
  • Rana catesbeiana
  • Physiology
  • Models, Biological
  • Mathematics
  • Hydrolysis
  • Cell Membrane
  • Animals
  • 3208 Medical physiology
 

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Dumke, C. L., Arshavsky, V. Y., Calvert, P. D., Bownds, M. D., & Pugh, E. N. (1994). Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase. J Gen Physiol, 103(6), 1071–1098. https://doi.org/10.1085/jgp.103.6.1071
Dumke, C. L., V. Y. Arshavsky, P. D. Calvert, M. D. Bownds, and E. N. Pugh. “Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase.J Gen Physiol 103, no. 6 (June 1994): 1071–98. https://doi.org/10.1085/jgp.103.6.1071.
Dumke CL, Arshavsky VY, Calvert PD, Bownds MD, Pugh EN. Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase. J Gen Physiol. 1994 Jun;103(6):1071–98.
Dumke, C. L., et al. “Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase.J Gen Physiol, vol. 103, no. 6, June 1994, pp. 1071–98. Pubmed, doi:10.1085/jgp.103.6.1071.
Dumke CL, Arshavsky VY, Calvert PD, Bownds MD, Pugh EN. Rod outer segment structure influences the apparent kinetic parameters of cyclic GMP phosphodiesterase. J Gen Physiol. 1994 Jun;103(6):1071–1098.

Published In

J Gen Physiol

DOI

ISSN

0022-1295

Publication Date

June 1994

Volume

103

Issue

6

Start / End Page

1071 / 1098

Location

United States

Related Subject Headings

  • Rod Cell Outer Segment
  • Rhodopsin
  • Rana catesbeiana
  • Physiology
  • Models, Biological
  • Mathematics
  • Hydrolysis
  • Cell Membrane
  • Animals
  • 3208 Medical physiology