Gating-Associated Clustering-Dispersion Dynamics of the KcsA Potassium Channel in a Lipid Membrane

被引:27
|
作者
Sumino, Ayumi [1 ,2 ]
Yamamoto, Daisuke [3 ]
Iwamoto, Masayuki [2 ]
Dewa, Takehisa [4 ]
Oiki, Shigetoshi [2 ]
机构
[1] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
[2] Univ Fukui, Fac Med Sci, Dept Mol Physiol & Biophys, Fukui 9101193, Japan
[3] Fukuoka Univ, Dept Appl Phys, Fukuoka 8140180, Japan
[4] Nagoya Inst Technol, Grad Sch Engn, Dept Frontier Mat, Showa Ku, Nagoya, Aichi 4668555, Japan
来源
关键词
ATOMIC-FORCE MICROSCOPY; HIGH-RESOLUTION AFM; PROTEINS; REARRANGEMENTS; DOMAINS; RAFTS; MODEL; VISUALIZATION; ACTIVATION; BILAYERS;
D O I
10.1021/jz402491t
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The KcsA potassium channel is a prototypical channel of bacterial origin, and the mechanism underlying the pH-dependent gating has been studied extensively. With the high-resolution atomic force microscopy (AFM), we have resolved functional open and closed gates of the KcsA channel under the membrane-embedded condition. Here we surprisingly found that the pH-dependent gating of the KcsA channels was associated with clustering-dispersion, dynamics. At neutral pH, the resting, closed channels were coalesced, forming nanoclusters. At acidic pH, the open-gated channels were dispersed as singly isolated channels. Time-lapse AFM revealed reversible clustering dispersion transitions upon pH changes. At acidic equilibrium, a small fraction of the channels was nanoclustered, in which the gate was apparently closed. Thus, it is suggested that opening of the gate and the dispersion are tightly linked. The interplay between the intramolecular conformational change and the supramolecular clustering-dispersion dynamics provides insights into understanding of unprecedented functional cooperativity of channels.
引用
收藏
页码:578 / 584
页数:7
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