Multiple residues specify external tetraethylammonium blockade in voltage-gated potassium channels.

AUTOR(ES)

Pascual, J M

RESUMO

We have mapped residues in the carboxyl half of the P region of a voltage-gated K+ channel that influence external tetraethylammonium (TEA) block. Fifteen amino acids were substituted with cysteine and expressed in oocytes from monomeric or heterodimeric cRNAs. From a total of six mutant channels with altered TEA sensitivity, three were susceptible to modification by extracellularly applied charged methanethiosulfonates (MTSX). Another residue did not affect TEA block but was protected from MTSX by TEA. MTSX modification of position Y380C, thought to form the TEA binding site, affected TEA affinity only moderately, and this effect could be reversed by additional charge transfer from an oppositely charged MTSX analog. The results show that TEA block is modulated from multiple sites, including residues located deep in the pore and that several side chains besides that of Y380 are exposed at the TEA receptor.

Documentos Relacionados

• Voltage-gated and inwardly rectifying potassium channels
• Hydrophobic mutations alter the movement of Mg2+ in the pore of voltage-gated potassium channels.
• Hypoxic pulmonary vasoconstriction: role of voltage-gated potassium channels
• VKCDB: Voltage-gated potassium channel database
• A molecular blueprint for the pore-forming structure of voltage-gated calcium channels.