PT  - JOURNAL ARTICLE
AU  - Andrei Kondratiev
AU  - Gordon F. Tomaselli
TI  - Altered Gating and Local Anesthetic Block Mediated by Residues in the  I-S6 and II-S6 Transmembrane Segments of Voltage-Dependent Na<sup>+</sup>  Channels
AID  - 10.1124/mol.64.3.741
DP  - 2003 Sep 01
TA  - Molecular Pharmacology
PG  - 741--752
VI  - 64
IP  - 3
4099  - http://molpharm.aspetjournals.org/content/64/3/741.short
4100  - http://molpharm.aspetjournals.org/content/64/3/741.full
SO  - Mol Pharmacol2003 Sep 01; 64
AB  - The cytoplasmic side of the voltage-dependent Na+ channel pore is putatively formed by the S6 segments of domains I to IV. The role of amino acid residues of I-S6 and II-S6 in channel gating and local anesthetic (LA) block was investigated using the cysteine scanning mutagenesis of the rat skeletal muscle Na+ channel (Nav1.4). G428C uniquely reduced sensitivity to rested state or first-pulse block by lidocaine without alterations in the voltage dependence or kinetics of gating that would otherwise account for the increase in the IC50 for block. Mutations in I-S6 (N434C and I436C) and in II-S6 (L785C and V787C) increased sensitivity to first-pulse block by lidocaine. Enhanced inactivation accounted for the increased sensitivity of N434C to lidocaine and hastening of inactivation of I436C in the absence of drug could account for higher affinity first-pulse block. Mutations in I-S6 (I424C, I425C, and F430C) and in II-S6 (I782C and V786C) reduced the use-dependent lidocaine block. The reduction in use-dependent block of F430C was consistent with alterations in inactivation gating; the other mutants did not exhibit gating changes that could explain the reduced sensitivity to lidocaine. Therefore, several amino acids (I424, I425, G428, I782, and V786), in addition to those previously identified (Yarov-Yarovoy et al., 2002), alter the sensitivity of Nav1.4 to lidocaine, independent of mutation-induced changes in gating. The magnitude of the change in the IC50 values, the isoform, and LA dependence of the changes in affinity suggest that the determinants of binding in I-S6 and II-S6 are subsidiary to those in IV-S6.