help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on June 1, 2007.
doi:10.1529/biophysj.107.104349
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.107.104349v1
93/7/2307    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Broomand, A.
Right arrow Articles by Elinder, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Broomand, A.
Right arrow Articles by Elinder, F.
Biophysical Journal 93:2307-2314 (2007)
© 2007 The Biophysical Society

Electrostatic Domino Effect in the Shaker K Channel Turret

Amir Broomand *, Fredrik Österberg *, Tara Wardi {dagger} and Fredrik Elinder *

* Department of Biomedicine and Surgery, Division of Cell Biology, Linköpings Universitet, Linköping, Sweden; and {dagger} Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden

Correspondence: Address reprint requests to Fredrik Elinder, Tel.: 46-13-22-89-45; E-mail: fredrik.elinder{at}ibk.liu.se.

Voltage-gated K channels are regulated by extracellular divalent cations such as Mg2+ and Sr2+, either by screening of fixed negative surface charges, by binding directly or close to the voltage sensor, or by binding to the pore. Different K channels display different sensitivity to divalent cations. For instance, 20 mM MgCl2 shifts the conductance versus voltage curve, G(V), of the Kv1-type Shaker channel with 14 mV, while the G(V) of Kv2.1 is shifted only with 7 mV. This shift difference is paralleled with different working ranges. Kv1-type channels open at ~–20 mV and Kv2.1 channel open at ~+5 mV. The aim of this study was to identify critical residues for this Mg2+-induced G(V) shift by introducing Kv2.1 channel residues in the Shaker K channel. The K channels were expressed in Xenopus laevis oocytes and studied with the two-electrode voltage-clamp technique. We found that three neutral-to-positive amino-acid residue exchanges in the extracellular loops connecting transmembrane segments S5 and S6 transferred the Mg2+-shifting properties. The contributions of the three residues were additive, and thus independent of each other, with the contributions in the order 425 > 419 > 451. Charging 425 and 419 not only affect the Mg2+-induced G(V) shift with 5–6 mV, but also shifts the G(V) with 17 mV. Thus, a few strategically placed surface charges clearly modulate the channel's working range. Residue 425, located at some distance away from the voltage sensor, was shown to electrostatically affect residue K427, which in turn affects the voltage sensor S4—thus, an electrostatic domino effect.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Biophysical Society.