Literature DB >> 1940846

Single channel studies of the phosphorylation of K+ channels in the squid giant axon. I. Steady-state conditions.

E Perozo1, C A Vandenberg, D S Jong, F Bezanilla.   

Abstract

Phosphorylation of the delayed rectifier channel of squid potentiates the macroscopic K+ current and slows its activation kinetics. We have studied this phenomenon at the single channel level using the cut-open axon technique under steady-state conditions. In 10 mM external K+/310 mM internal K+ there are predominantly two types of channels present, a 20-pS and a 40-pS channel. In steady state at depolarized potentials, the 40-pS channel was most active, whereas the 20-pS channel tended to disappear due to a slow inactivation process. Two methods were developed to shift the population of channels toward a dephosphorylated state. One method consisted of predialyzing a whole axon with solutions containing no ATP, while recording the currents under axial-wire voltage clamp. A piece of axon was then removed and cut open, and single channel currents were recorded from the cut-open axon. A second method was based on the difference in diffusion coefficients for ATP and proteins such as the endogenous phosphatase. The axon was cut open in a solution that did not contain Ca2+ or Cl- in order to maintain the axoplasm structurally intact and permit endogenous phosphatase to act on the membrane while ATP diffused away, before removing the axoplasm and forming a membrane patch. When dephosphorylating conditions were used, the steady-state open probability of the 40-pS channel at 42 mV was very low (less than 0.0002), and the channel openings appeared as a series of infrequent, short-duration events. The channel activity was increased up to 150-fold by photoreleasing caged ATP inside the patch pipette in the presence of the catalytic subunit of protein kinase A. The sharp increase in open probability could be accounted for by a decrease of the slow component of the closed time distribution from 23 s to 170 ms with little change in the distribution of open times (1-2 ms) and no change in the single channel current amplitude. In voltage-jump experiments the contribution of the 40-pS channel to the delayed rectifier current was often small due to the large values of the latency to the first opening.

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Year:  1991        PMID: 1940846      PMCID: PMC2229041          DOI: 10.1085/jgp.98.1.1

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  7 in total

1.  An activation gating switch in Kv1.2 is localized to a threonine residue in the S2-S3 linker.

Authors:  Saman Rezazadeh; Harley T Kurata; Thomas W Claydon; Steven J Kehl; David Fedida
Journal:  Biophys J       Date:  2007-08-31       Impact factor: 4.033

Review 2.  Phosphorylation of K+ channels in the squid giant axon. A mechanistic analysis.

Authors:  E Perozo; F Bezanilla
Journal:  J Bioenerg Biomembr       Date:  1991-08       Impact factor: 2.945

3.  Molecular identification of SqKv1A. A candidate for the delayed rectifier K channel in squid giant axon.

Authors:  J J Rosenthal; R G Vickery; W F Gilly
Journal:  J Gen Physiol       Date:  1996-09       Impact factor: 4.086

Review 4.  Voltage-dependent K(+) channels in pancreatic beta cells: role, regulation and potential as therapeutic targets.

Authors:  P E MacDonald; M B Wheeler
Journal:  Diabetologia       Date:  2003-06-27       Impact factor: 10.122

5.  Voltage-insensitive gating after charge-neutralizing mutations in the S4 segment of Shaker channels.

Authors:  H Bao; A Hakeem; M Henteleff; J G Starkus; M D Rayner
Journal:  J Gen Physiol       Date:  1999-01       Impact factor: 4.086

6.  Potassium channels in squid neuron cell bodies: comparison to axonal channels.

Authors:  T Nealey; S Spires; R A Eatock; T Begenisich
Journal:  J Membr Biol       Date:  1993-02       Impact factor: 1.843

7.  Microscopic heterogeneity in unitary N-type calcium currents in rat sympathetic neurons.

Authors:  A R Rittenhouse; P Hess
Journal:  J Physiol       Date:  1994-01-01       Impact factor: 5.182

  7 in total

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