Cymes Gisela D, Grosman Claudio, Auerbach Anthony
Center for Single-Molecule Biophysics and Department of Physiology and Biophysics, State University of New York at Buffalo, Buffalo, New York 14214, USA.
Biochemistry. 2002 Apr 30;41(17):5548-55. doi: 10.1021/bi011864f.
The gating mechanism of the acetylcholine receptor channel (AChR) was investigated by using rate equilibrium linear free energy relationships (LFERs) to probe the transition state between the closed and open conformations. The properties of the transition state of gating in the second transmembrane segment (M2) of the delta subunit, one of the five homologous pore-lining segments, was measured on a residue-by-residue basis. Series of point mutations were engineered at individual positions of this domain, and the corresponding constructs were characterized electrophysiologically, at the single-channel level. Fully liganded AChR opening and closing rate constants were estimated, and Phi-values (which are a measure of the extent of the conformational change realized at the transition state) were calculated for each reaction series as the slope of the Brønsted relationship (log rate constant versus log equilibrium constant). Our results indicate that, at the transition state of gating, the extracellular half of deltaM2 partly resembles the open state (Phi-values between 0.24 and 0.38) while the intracellular half completely resembles the closed state (Phi-values between -0.18 and 0.03), with a break point near the middle of the M2 segment. This suggests that during gating the two halves of deltaM2 move asynchronously, with the rearrangement of the extracellular portion preceding (following) that of the intracellular part of deltaM2 during opening (closing). This particular sequence of molecular events indicates that the gating conformational change, which starts at the extracellular acetylcholine-binding sites (when opening), does not propagate exclusively along the primary sequence of the protein. In addition, our data are consistent with the deltaM2 segment bending or swiveling around its central residues during gating. We also elaborate on unsettled aspects of the analysis such as the accuracy of two-point LFERs, the physical interpretation of fractional Phi-values, and the existence of single versus parallel transition states for the gating reaction.
通过使用速率平衡线性自由能关系(LFERs)来探究乙酰胆碱受体通道(AChR)的门控机制,以探测关闭和开放构象之间的过渡态。在五个同源孔道内衬片段之一的δ亚基的第二个跨膜片段(M2)中,逐个残基地测量门控过渡态的性质。在该结构域的各个位置设计了一系列点突变,并在单通道水平上对相应构建体进行了电生理特性表征。估计了完全结合配体的AChR的开放和关闭速率常数,并针对每个反应系列计算了Phi值(它是在过渡态实现的构象变化程度的一种度量),作为布朗斯特关系(对数速率常数与对数平衡常数)的斜率。我们的结果表明,在门控过渡态时,δM2的细胞外一半部分类似于开放状态(Phi值在0.24和0.38之间),而细胞内一半完全类似于关闭状态(Phi值在-0.18和0.03之间),在M2片段中间附近有一个断点。这表明在门控过程中,δM2的两半异步移动,在开放(关闭)过程中,δM2细胞外部分的重排先于(后于)细胞内部分。这种特定的分子事件序列表明,从细胞外乙酰胆碱结合位点开始(开放时)的门控构象变化并非仅沿着蛋白质的一级序列传播。此外,我们的数据与门控过程中δM2片段围绕其中心残基弯曲或旋转一致。我们还详细阐述了分析中未解决的方面,如两点LFERs的准确性、分数Phi值的物理解释以及门控反应单过渡态与平行过渡态的存在。