Literature DB >> 8133245

Interactions of amino terminal domains of Shaker K channels with a pore blocking site studied with synthetic peptides.

R D Murrell-Lagnado1, R W Aldrich.   

Abstract

Synthetic peptides of the five alternative NH2-terminal sequences of Shaker when applied to the cytoplasmic side of ShB channels that have an NH2-terminal deletion (ShB delta 6-46) block the channel with potencies correlated with the rate of inactivation in the corresponding variant. These peptides share no sequence similarity and yet three out of the five have apparent dissociation constants between 2 and 15 microM, suggesting that the specificity requirements for binding are low. To identify the primary structural determinants required for effective block of ShB delta 6-46, we examined the effects of substitutions made to the 20 residue ShB peptide on association and dissociation rates. Nonpolar residues within the peptide appear to be important in stabilizing the binding through hydrophobic interactions. Substitutions to leucine-7 showed there was a clear correlation between hydrophobicity and the dissociation rate constant (koff) with little effect on the association rate constant (kon). Substituting charged residues for hydrophobic residues within the region 4-8 disrupted binding. Within the COOH-terminal half of the peptide, substitutions that increased the net positive charge increased kon with relatively small changes in koff, suggesting the involvement of long-range electrostatic interactions in increasing the effective concentration of the peptide. Neutralizing charged residues produced small changes in koff. Charges within the region 12-20 act equivalently; alterations which conserved net charge produced little effect on either kon or koff. The results are consistent with this region of the peptide having an extended conformation and suggest that when bound this region makes few contacts with the channel protein and remains relatively unconstrained. Analogous mutations within the NH2-terminal domain of the intact ShB channel produced qualitatively similar effects on blocking and unblocking rates.

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Year:  1993        PMID: 8133245      PMCID: PMC2229190          DOI: 10.1085/jgp.102.6.949

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  62 in total

1.  Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homolog.

Authors:  M Wallner; P Meera; L Toro
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

2.  Three-dimensional structure of the S4-S5 segment of the Shaker potassium channel.

Authors:  Oliver Ohlenschläger; Hironobu Hojo; Ramadurai Ramachandran; Matthias Görlach; Parvez I Haris
Journal:  Biophys J       Date:  2002-06       Impact factor: 4.033

3.  Frequency-dependent inactivation of mammalian A-type K+ channel KV1.4 regulated by Ca2+/calmodulin-dependent protein kinase.

Authors:  J Roeper; C Lorra; O Pongs
Journal:  J Neurosci       Date:  1997-05-15       Impact factor: 6.167

4.  N-type inactivation features of Kv4.2 channel gating.

Authors:  Manuel Gebauer; Dirk Isbrandt; Kathrin Sauter; Britta Callsen; Andreas Nolting; Olaf Pongs; Robert Bähring
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

Review 5.  Mechanisms of closed-state inactivation in voltage-gated ion channels.

Authors:  Robert Bähring; Manuel Covarrubias
Journal:  J Physiol       Date:  2010-11-22       Impact factor: 5.182

Review 6.  A role for A-to-I RNA editing in temperature adaptation.

Authors:  Sandra C Garrett; Joshua J C Rosenthal
Journal:  Physiology (Bethesda)       Date:  2012-12

7.  STIM1 gates TRPC channels, but not Orai1, by electrostatic interaction.

Authors:  Weizhong Zeng; Joseph P Yuan; Min Seuk Kim; Young Jin Choi; Guo N Huang; Paul F Worley; Shmuel Muallem
Journal:  Mol Cell       Date:  2008-11-07       Impact factor: 17.970

8.  A novel N-terminal motif of dipeptidyl peptidase-like proteins produces rapid inactivation of KV4.2 channels by a pore-blocking mechanism.

Authors:  Henry H Jerng; Kevin Dougherty; Manuel Covarrubias; Paul J Pfaffinger
Journal:  Channels (Austin)       Date:  2009-11-30       Impact factor: 2.581

9.  Comparative study of the gating motif and C-type inactivation in prokaryotic voltage-gated sodium channels.

Authors:  Katsumasa Irie; Kazuya Kitagawa; Hitoshi Nagura; Tomoya Imai; Takushi Shimomura; Yoshinori Fujiyoshi
Journal:  J Biol Chem       Date:  2009-12-03       Impact factor: 5.157

10.  Constitutive activation of the Shaker Kv channel.

Authors:  Manana Sukhareva; David H Hackos; Kenton J Swartz
Journal:  J Gen Physiol       Date:  2003-10-13       Impact factor: 4.086

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