AbstractVoltage-dependent movement of a sodium channel S4 segment was examined by cysteine scanning mutagenesis and testing accessibility of the residues to hydrophilic cysteine-modifying reagents. These experiments indicate that 2 charged S4 residues move completely from an internally accessible to an externally accessible location in response to depolarization by passage through a short “channel” in the protein. The energetic problems of S4 movement have thus been solved in the same way that many ion channels achieve highly selective and rapid ion permeation through an open pore, by restricting the contact region between the permion and its channel
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human ske...
The fourth segment of domain 4 (S4/D4) in Na+ channels is a voltage sensor especially implicated in ...
AbstractThe role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is ...
AbstractVoltage-dependent movement of a sodium channel S4 segment was examined by cysteine scanning ...
AbstractThe mutation R1448C substitutes a cysteine for the outermost arginine in the fourth transmem...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
The role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is less doc...
The role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is less doc...
Much data, including crystallographic, support structural models of sodium and potassium channels co...
PubMedID: 19878047The hERG potassium channel is a member of the voltage gated potassium (Kv) channel...
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human ske...
Much data, including crystallographic, support structural models of sodium and potassium channels co...
AbstractThe mutation R1448C substitutes a cysteine for the outermost arginine in the fourth transmem...
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human ske...
The fourth segment of domain 4 (S4/D4) in Na+ channels is a voltage sensor especially implicated in ...
AbstractThe role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is ...
AbstractVoltage-dependent movement of a sodium channel S4 segment was examined by cysteine scanning ...
AbstractThe mutation R1448C substitutes a cysteine for the outermost arginine in the fourth transmem...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane...
The role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is less doc...
The role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is less doc...
Much data, including crystallographic, support structural models of sodium and potassium channels co...
PubMedID: 19878047The hERG potassium channel is a member of the voltage gated potassium (Kv) channel...
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human ske...
Much data, including crystallographic, support structural models of sodium and potassium channels co...
AbstractThe mutation R1448C substitutes a cysteine for the outermost arginine in the fourth transmem...
The second and third basic residues of the S4 segment of domain 4 (D4:R2 and D4:R3) of the human ske...
The fourth segment of domain 4 (S4/D4) in Na+ channels is a voltage sensor especially implicated in ...
AbstractThe role of hydrophobic residues in voltage sensors S4 of voltage-sensitive ion channels is ...