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CMP
Credit: Jack Hobhouse

Professor Stephen Tucker

Professor of Biophysics

Research theme

  • Biological physics

Sub department

  • Condensed Matter Physics

Research groups

  • Ion channels
Stephen.Tucker@physics.ox.ac.uk
Telephone: 01865 (2)72382
Biochemistry Building, room 30-090 Kavli Institute, DCHB
  • About
  • Publications

Functional analysis of missense variants in the TRESK (KCNK18) K channel.

Sci Rep 2 (2012) 237

Authors:

Isabelle Andres-Enguix, Lijun Shang, Phillip J Stansfeld, Julia M Morahan, Mark SP Sansom, Ronald G Lafrenière, Bishakha Roy, Lyn R Griffiths, Guy A Rouleau, George C Ebers, Zameel M Cader, Stephen J Tucker

Abstract:

A loss of function mutation in the TRESK K2P potassium channel (KCNK18), has recently been linked with typical familial migraine with aura. We now report the functional characterisation of additional TRESK channel missense variants identified in unrelated patients. Several variants either had no apparent functional effect, or they caused a reduction in channel activity. However, the C110R variant was found to cause a complete loss of TRESK function, yet is present in both sporadic migraine and control cohorts, and no variation in KCNK18 copy number was found. Thus despite the previously identified association between loss of TRESK channel activity and migraine in a large multigenerational pedigree, this finding indicates that a single non-functional TRESK variant is not alone sufficient to cause typical migraine and highlights the genetic complexity of this disorder.
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State-independent intracellular access of quaternary ammonium blockers to the pore of TREK-1.

Channels (Austin) 6:6 (2012) 473-478

Authors:

Markus Rapedius, Matthias R Schmidt, Chetan Sharma, Phillip J Stansfeld, Mark SP Sansom, Thomas Baukrowitz, Stephen J Tucker

Abstract:

We previously reported that TREK-1 gating by internal pH and pressure occurs close to or within the selectivity filter. These conclusions were based upon kinetic measurements of high-affinity block by quaternary ammonium (QA) ions that appeared to exhibit state-independent accessibility to their binding site within the pore. Intriguingly, recent crystal structures of two related K2P potassium channels were also both found to be open at the helix bundle crossing. However, this did not exclude the possibility of gating at the bundle crossing and it was suggested that side-fenestrations within these structures might allow state-independent access of QA ions to their binding site. In this addendum to our original study we demonstrate that even hydrophobic QA ions do not access the TREK-1 pore via these fenestrations. Furthermore, by using a chemically reactive QA ion immobilized within the pore via covalent cysteine modification we provide additional evidence that the QA binding site remains accessible to the cytoplasm in the closed state. These results support models of K2P channel gating which occur close to or within the selectivity filter and do not involve closure at the helix bundle crossing.
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Structural and Mechanistic Insights into Gating of K2P Channels

BIOPHYSICAL JOURNAL 102:3 (2012) 121A-121A

Authors:

Markus Rapedius, Paula L Piechotta, Philip J Stansfeld, Murali K Bollepalli, Gunter Ehrlich, Isabelle Andres-Enguix, Hariolf Fritzenschaft, Niels Decher, Mark SP Sansom, Stephen J Tucker, Thomas Baukrowitz
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The pore structure and gating mechanism of K2P channels

The EMBO Journal Springer Science and Business Media LLC 30:21 (2011) 4515-4515

Authors:

Paula L Piechotta, Markus Rapedius, Phillip J Stansfeld, Murali K Bollepalli, Gunter Ehrlich, Isabelle Andres-Enguix, Hariolf Fritzenschaft, Niels Decher, Mark SP Sansom, Stephen J Tucker, Thomas Baukrowitz
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The pore structure and gating mechanism of K2P channels

The EMBO journal 30:21 (2011) 4515-4515
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