共 50 条
Sequential formation of ion pairs during activation of a sodium channel voltage sensor
被引:108
作者:
DeCaen, Paul G.
[1
]
Yarov-Yarovoy, Vladimir
[1
]
Sharp, Elizabeth M.
[1
]
Scheuer, Todd
[1
]
Catterall, William A.
[1
]
机构:
[1] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
来源:
基金:
美国国家卫生研究院;
关键词:
electrical excitability;
gating;
SHAKER K+ CHANNEL;
GATING CHARGE;
ELECTROSTATIC INTERACTIONS;
POTASSIUM CHANNEL;
PROTEIN STABILITY;
DISULFIDE BONDS;
SCORPION TOXIN;
NA+ CHANNELS;
WILD-TYPE;
MOVEMENT;
D O I:
10.1073/pnas.0912307106
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Electrical signaling in biology depends upon a unique electromechanical transduction process mediated by the S4 segments of voltage-gated ion channels. These transmembrane segments are driven outward by the force of the electric field on positively charged amino acid residues termed "gating charges," which are positioned at three-residue intervals in the S4 transmembrane segment, and this movement is coupled to opening of the pore. Here, we use the disulfide-locking method to demonstrate sequential ion pair formation between the fourth gating charge in the S4 segment (R4) and two acidic residues in the S2 segment during activation. R4 interacts first with E70 at the intracellular end of the S2 segment and then with D60 near the extracellular end. Analysis with the Rosetta Membrane method reveals the 3-D structures of the gating pore as these ion pairs are formed sequentially to catalyze the S4 transmembrane movement required for voltage-dependent activation. Our results directly demonstrate sequential ion pair formation that is an essential feature of the sliding helix model of voltage sensor function but is not compatible with the other widely discussed gating models.
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页码:22498 / 22503
页数:6
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