|
||
The Journal of General Physiology, Vol 101, 1-25, Copyright © 1993 by The Rockefeller University Press
ARTICLES |
JW Karpen, RL Brown, L Stryer and DA Baylor
Department of Neurobiology, Sherman Fairchild Center, Stanford University School of Medicine, California 94305.
The effects of divalent cations on the gating of the cGMP-activated channel, and the effects of gating on the movement of divalent cations in and out of the channel's pore were studied by recording macroscopic currents in excised membrane patches from salamander retinal rods. The fractional block of cGMP-activated Na+ currents by internal and external Mg2+ as well as internal Ca2+ was nearly independent of cGMP concentration. This indicates that Mg2+ and Ca2+ bind with similar affinity to open and closed states of the channel. In contrast, the efficiency of block by internal Cd2+ or Zn2+ increased in proportion to the fraction of open channels, indicating that these ions preferentially occupy open channels. The kinetics of block by internal Ni2+, which competes with Mg2+ but blocks more slowly, were found to be unaffected by the fraction of channels open. External Ni2+, however, blocked and unblocked much more rapidly when channels were mostly open. This suggests that within the pore a gate is located between the binding site(s) for ions and the extracellular mouth of the channel. Micromolar concentrations of the transition metal divalent cations Ni2+, Cd2+, Zn2+, and Mn2+ applied to the cytoplasmic surface of a patch potentiated the response to subsaturating concentrations of cGMP without affecting the maximum current induced by saturating cGMP. The concentration of cGMP that opened half the channels was often lowered by a factor of three or more. Potentiation persisted after the experimental chamber was washed with divalent-free solution and fresh cGMP was applied, indicating that it does not result from an interaction between divalent cations and cGMP in solution; 1 mM EDTA or isotonic MgCl2 reversed potentiation. Voltage-jump experiments suggest that potentiation results from an increase in the rate of cGMP binding. Lowering the ionic strength of the bathing solution enhanced potentiation, suggesting that it involves electrostatic interactions. The strong electrostatic effect on cGMP binding and absence of effect on ion permeation through open channels implies that the cGMP binding sites on the channel are well separated from the permeation pathway.
This article has been cited by other articles:
![]() |
S. Krannich and M. Stengl Cyclic Nucleotide-Activated Currents in Cultured Olfactory Receptor Neurons of the Hawkmoth Manduca sexta J Neurophysiol, November 1, 2008; 100(5): 2866 - 2877. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Contreras, D. Srikumar, and M. Holmgren Gating at the selectivity filter in cyclic nucleotide-gated channels PNAS, March 4, 2008; 105(9): 3310 - 3314. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Alam, N. Shi, and Y. Jiang Structural insight into Ca2+ specificity in tetrameric cation channels PNAS, September 25, 2007; 104(39): 15334 - 15339. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Wilkens and R. W. Aldrich State-independent Block of BK Channels by an Intracellular Quaternary Ammonium J. Gen. Physiol., August 28, 2006; 128(3): 347 - 364. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Zimmerman Capturing Ion Channel Gating: A Little Salt on the Tail Does the Trick J. Gen. Physiol., November 29, 2004; 124(6): 627 - 629. [Full Text] [PDF] |
||||
![]() |
U. B. Kaupp and R. Seifert Cyclic Nucleotide-Gated Ion Channels Physiol Rev, July 1, 2002; 82(3): 769 - 824. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Savchenko, T. W. Kraft, E. Molokanova, and R. H. Kramer Growth factors regulate phototransduction in retinal rods by modulating cyclic nucleotide-gated channels through dephosphorylation of a specific tyrosine residue PNAS, April 18, 2001; (2001) 101524998. [Abstract] [Full Text] |
||||
![]() |
B. H. Grahn, P. G. Paterson, K. T. Gottschall-Pass, and Z. Zhang Zinc and the Eye J. Am. Coll. Nutr., April 1, 2001; 20(2): 106 - 118. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Kramer and E. Molokanova Modulation of cyclic-nucleotide-gated channels and regulation of vertebrate phototransduction J. Exp. Biol., January 9, 2001; 204(17): 2921 - 2931. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. He, M. Ruiz, and J. W. Karpen Constraining the subunit order of rod cyclic nucleotide-gated channels reveals a diagonal arrangement of like subunits PNAS, January 18, 2000; 97(2): 895 - 900. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Molokanova, B. Trivedi, A. Savchenko, and R. H. Kramer Modulation of Rod Photoreceptor Cyclic Nucleotide-Gated Channels by Tyrosine Phosphorylation J. Neurosci., December 1, 1997; 17(23): 9068 - 9076. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Qian, L. Li, R. L. Chappell, and H. Ripps GABA Receptors of Bipolar Cells From the Skate Retina: Actions of Zinc on GABA-Mediated Membrane Currents J Neurophysiol, November 1, 1997; 78(5): 2402 - 2412. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Savchenko, T. W. Kraft, E. Molokanova, and R. H. Kramer Growth factors regulate phototransduction in retinal rods by modulating cyclic nucleotide-gated channels through dephosphorylation of a specific tyrosine residue PNAS, May 8, 2001; 98(10): 5880 - 5885. [Abstract] [Full Text] [PDF] |
||||
|
|