Literature DB >> 7682009

Extracellular access to the Na,K pump: pathway similar to ion channel.

D C Gadsby1, R F Rakowski, P De Weer.   

Abstract

In each normal Na,K pump cycle, first three sodium and then two potassium ions are transported; in both cases, the ions become temporarily occluded in pump conformations that isolate them from internal and external solutions. A major charge movement occurs during sodium translocation and accompanies the deocclusion of sodium ions or their release to the cell exterior, or both. The nature of the charge movement was examined by measurement of the undirectional sodium-22 efflux mediated by Nai-Nao exchange (Nai and Nao are internal and external sodium ions) in voltage-clamped, internally dialyzed squid giant axons in the absence of potassium; in this way the pump activity was restricted to the sodium-translocation pathway. Although electroneutral, the Nai-Nao exchange was nevertheless voltage-sensitive: increasingly negative potentials enhanced its rate along a saturating sigmoid curve. Such voltage dependence demonstrates that the release and rebinding of external sodium is the predominant charge-moving (hence, voltage-sensitive) step, suggesting that extracellular sodium ions must reach their binding sites deep in the pump molecule through a high-field access channel. This implies that part of the pump molecule is functionally analogous to an ion channel.

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Year:  1993        PMID: 7682009     DOI: 10.1126/science.7682009

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  75 in total

1.  Structure of Na+,K+-ATPase at 11-A resolution: comparison with Ca2+-ATPase in E1 and E2 states.

Authors:  W J Rice; H S Young; D W Martin; J R Sachs; D L Stokes
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

2.  Na(+) transport, and the E(1)P-E(2)P conformational transition of the Na(+)/K(+)-ATPase.

Authors:  A Babes; K Fendler
Journal:  Biophys J       Date:  2000-11       Impact factor: 4.033

Review 3.  Electrogenic properties of the Na+,K+-ATPase probed by presteady state and relaxation studies.

Authors:  E Bamberg; R J Clarke; K Fendler
Journal:  J Bioenerg Biomembr       Date:  2001-10       Impact factor: 2.945

4.  Voltage dependence of the apparent affinity for external Na(+) of the backward-running sodium pump.

Authors:  P De Weer; D C Gadsby; R F Rakowski
Journal:  J Gen Physiol       Date:  2001-04       Impact factor: 4.086

5.  Na+/K+-pump ligands modulate gating of palytoxin-induced ion channels.

Authors:  Pablo Artigas; David C Gadsby
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-23       Impact factor: 11.205

6.  Effect of extracellular pH on presteady-state and steady-state current mediated by the Na+/K+ pump.

Authors:  A Vasilyev; K Khater; R F Rakowski
Journal:  J Membr Biol       Date:  2004-03-15       Impact factor: 1.843

7.  Effect of ADP on Na(+)-Na(+) exchange reaction kinetics of Na,K-ATPase.

Authors:  R Daniel Peluffo
Journal:  Biophys J       Date:  2004-08       Impact factor: 4.033

8.  Energy landscape of the reactions governing the Na+ deeply occluded state of the Na+/K+-ATPase in the giant axon of the Humboldt squid.

Authors:  Juan P Castillo; Daniela De Giorgis; Daniel Basilio; David C Gadsby; Joshua J C Rosenthal; Ramon Latorre; Miguel Holmgren; Francisco Bezanilla
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-05       Impact factor: 11.205

9.  A third Na+-binding site in the sodium pump.

Authors:  Ciming Li; Oihana Capendeguy; Käthi Geering; Jean-Daniel Horisberger
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-25       Impact factor: 11.205

10.  Involvement of the Na,K-ATPase in the induction of ion channels by palytoxin.

Authors:  S Y Kim; K A Marx; C H Wu
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-05       Impact factor: 3.000

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