When attached outside the voltage-sensing S4 segment of the Shaker potassium channel, the fluorescent probe tetramethylrhodamine (TMRM) undergoes voltage-dependent fluorescence changes (ΔF) due to differential interaction with a pH-titratable external protein-lined vestibule (Cha, A., and F. Bezanilla. 1998. J. Gen. Physiol. 112:391–408.). We attached TMRM at the same sites [corresponding to M356C and A359C in the wild-type (wt) channel] in a deletion mutant of Shaker where all but the five amino acids closest to S4 had been removed from the S3–S4 linker. In the deletion mutant, the maximal ΔF/F seen was diminished 10-fold, and the ΔF at M356C became pH independent, suggesting that the protein-lined vestibule is made up in large part by the S3–S4 linker. The residual ΔF showed that the probe still interacted with two putative quenching groups near the S4 segment. One group was detected by M356C-TMRM (located outside of S3 in the deletion mutant) and reported on deactivation gating charge movement when applying hyperpolarizing voltage steps from a holding potential of 0 mV. During activating voltage steps from a holding potential of −90 mV, the fluorescence lagged considerably behind the movement of gating charge over a range of potentials. Another putative quenching group was seen by probes attached closer to the S4 and caused a ΔF at extreme hyperpolarizations (more negative than −90 mV) only. A signal from the interaction with this group in the wt S3–S4 linker channel (at L361C) correlated with gating charge moving in the hyperpolarized part of the Q-V curve. Probe attached at A359C in the deletion mutant and at L361C in wt channel showed a biphasic ΔF as the probe oscillated between the two groups, revealing that there is a transient state of the voltage sensor in between, where the probe has maximal fluorescence. We conclude that the voltage sensor undergoes two distinct conformational changes as seen from probes attached outside the S4 segment.
Skip Nav Destination
Article navigation
1 February 2000
Article|
February 01 2000
Deletion of the S3–S4 Linker in theShaker Potassium Channel Reveals Two Quenching Groups near the outside of S4
J.B. Sørensen,
J.B. Sørensen
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
dAugust Krogh Institute, University of Copenhagen, Copenhagen, Denmark
Search for other works by this author on:
A. Cha,
A. Cha
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
Search for other works by this author on:
R. Latorre,
R. Latorre
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
cCentro de Estudios Cientificos de Santiago and Department of Biology, University of Chile, Santiago, 676470 Chile
Search for other works by this author on:
E. Rosenman,
E. Rosenman
cCentro de Estudios Cientificos de Santiago and Department of Biology, University of Chile, Santiago, 676470 Chile
Search for other works by this author on:
F. Bezanilla
F. Bezanilla
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
Search for other works by this author on:
J.B. Sørensen
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
dAugust Krogh Institute, University of Copenhagen, Copenhagen, Denmark
A. Cha
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
R. Latorre
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
cCentro de Estudios Cientificos de Santiago and Department of Biology, University of Chile, Santiago, 676470 Chile
E. Rosenman
cCentro de Estudios Cientificos de Santiago and Department of Biology, University of Chile, Santiago, 676470 Chile
F. Bezanilla
aDepartment of Physiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
bDepartment of Anesthesiology, University of California, Los Angeles School of Medicine, Los Angeles, California 90095
Portions of this work were previously published in abstract form (Sørensen, J.B., A. Cha, R. Latorre, E. Rosenmann, and F. Bezanilla. 1999. Biophys. J. 76:A411).
Abbreviations used in this paper: aa, amino acid; HP, holding potential; wt, wild type; TMRM, tetramethylrhodamine.
Due to false saturation of the Q-V, it was not possible to identify the exact magnitude of the displacement.
Received:
July 02 1999
Revision Requested:
January 05 2000
Accepted:
January 06 2000
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Gen Physiol (2000) 115 (2): 209–222.
Article history
Received:
July 02 1999
Revision Requested:
January 05 2000
Accepted:
January 06 2000
Citation
J.B. Sørensen, A. Cha, R. Latorre, E. Rosenman, F. Bezanilla; Deletion of the S3–S4 Linker in theShaker Potassium Channel Reveals Two Quenching Groups near the outside of S4. J Gen Physiol 1 February 2000; 115 (2): 209–222. doi: https://doi.org/10.1085/jgp.115.2.209
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Structural Implications of Fluorescence Quenching in the Shaker K+ Channel
J Gen Physiol (October,1998)
Normal and Mutant Rhodopsin Activation Measured with the Early Receptor Current in a Unicellular Expression System
J Gen Physiol (October,1999)
On the Mechanism by which 4-Aminopyridine Occludes Quinidine Block of the Cardiac K+ Channel, hKv1.5
J Gen Physiol (April,1998)
Email alerts
Advertisement