Laboratory of Molecular Neurobiology and Biophysics, Rockefeller University, Howard Hughes Medical Institute, 1230 York Avenue, New York, NY 10065, USA.
Science. 2009 Dec 18;326(5960):1668-74. doi: 10.1126/science.1180310.
Inward-rectifier potassium (K+) channels conduct K+ ions most efficiently in one direction, into the cell. Kir2 channels control the resting membrane voltage in many electrically excitable cells, and heritable mutations cause periodic paralysis and cardiac arrhythmia. We present the crystal structure of Kir2.2 from chicken, which, excluding the unstructured amino and carboxyl termini, is 90% identical to human Kir2.2. Crystals containing rubidium (Rb+), strontium (Sr2+), and europium (Eu3+) reveal binding sites along the ion conduction pathway that are both conductive and inhibitory. The sites correlate with extensive electrophysiological data and provide a structural basis for understanding rectification. The channel's extracellular surface, with large structured turrets and an unusual selectivity filter entryway, might explain the relative insensitivity of eukaryotic inward rectifiers to toxins. These same surface features also suggest a possible approach to the development of inhibitory agents specific to each member of the inward-rectifier K+ channel family.
内向整流钾 (K+) 通道在一个方向上最有效地传导 K+ 离子,即进入细胞。Kir2 通道控制着许多可兴奋细胞的静息膜电压,遗传性突变会导致周期性瘫痪和心律失常。我们展示了来自鸡的 Kir2.2 的晶体结构,除了无结构的氨基和羧基末端外,它与人类 Kir2.2 有 90%的同源性。含有铷 (Rb+)、锶 (Sr2+) 和铕 (Eu3+) 的晶体揭示了沿着离子传导途径的结合位点,这些位点既有传导性又有抑制性。这些位点与广泛的电生理学数据相关联,并为理解整流提供了结构基础。通道的细胞外表面有大的结构化炮塔和不寻常的选择性过滤器入口,这可能解释了真核内向整流器对毒素相对不敏感的原因。这些相同的表面特征也为开发针对内向整流钾通道家族每个成员的特异性抑制剂提供了一种可能的方法。