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Biophys J, August 2001, p. 814-826, Vol. 81, No. 2

U-Type Inactivation of Kv3.1 and Shaker Potassium Channels

Kathryn G. Klemic,* Glenn E. Kirsch,*dagger and Stephen W. Jones*

 *Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106 and  dagger Rammelkamp Center for Research, MetroHealth Medical Center, Cleveland, Ohio 44109 USA

We previously concluded that the Kv2.1 K+ channel inactivates preferentially from partially activated closed states. We report here that the Kv3.1 channel also exhibits two key features of this inactivation mechanism: a U-shaped voltage dependence measured at 10 s and stronger inactivation with repetitive pulses than with a single long depolarization. More surprisingly, slow inactivation of the Kv1 Shaker K+ channel (Shaker BDelta 6-46) also has a U-shaped voltage dependence for 10-s depolarizations. The time and voltage dependence of recovery from inactivation reveals two distinct components for Shaker. Strong depolarizations favor inactivation that is reduced by K<UP><SUB>o</SUB><SUP>+</SUP></UP> or by partial block by TEAo, as previously reported for slow inactivation of Shaker. However, depolarizations near 0 mV favor inactivation that recovers rapidly, with strong voltage dependence (as for Kv2.1 and 3.1). The fraction of channels that recover rapidly is increased in TEAo or high K<UP><SUB>o</SUB><SUP>+</SUP></UP>. We introduce the term U-type inactivation for the mechanism that is dominant in Kv2.1 and Kv3.1. U-type inactivation also makes a major but previously unrecognized contribution to slow inactivation of Shaker.

Biophys J, August 2001, p. 814-826, Vol. 81, No. 2
© 2001 by the Biophysical Society   0006-3495/01/08/814/13  $2.00



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