Kerr I D, Son H S, Sankararamakrishnan R, Sansom M S
Laboratory of Molecular Biophysics, University of Oxford, UK.
Biopolymers. 1996 Oct;39(4):503-15. doi: 10.1002/(SICI)1097-0282(199610)39:4%3C503::AID-BIP3%3E3.0.CO;2-0.
In the middle of the S6 helix in voltage-gated potassium channels there is a highly conserved Pro-Val-Pro motif, while the equivalent M2 helix of inward rectifier potassium channels contains a conserved glycine residue in a comparable position. The structural implications of these conserved motifs are of interest given the evidence that S6 and M2 are components of the lining of their respective pores. Multiple sequence alignment and TM helix prediction methods were used to define consensus regions for S6 and M2. Ensembles of 50 structures for each helix were generated by simulated annealing and restrained molecular dynamics. Time-dependent fluctuations of S6 and M2 were investigated by long time scale molecular dynamics simulations on representative members of each ensemble carried out in vacuo in the presence and absence of a hydrophobic potential that mimics a lipid bilayer. The results are discussed in terms of the structural basis of the kink in S6 and M2 and of a putative functional role for flexible helices as "molecular swivels."
在电压门控钾通道的S6螺旋中部,有一个高度保守的脯氨酸-缬氨酸-脯氨酸基序,而内向整流钾通道的等效M2螺旋在类似位置含有一个保守的甘氨酸残基。鉴于有证据表明S6和M2是其各自孔道内衬的组成部分,这些保守基序的结构意义备受关注。使用多序列比对和跨膜螺旋预测方法来定义S6和M2的共有区域。通过模拟退火和受限分子动力学生成每个螺旋的50个结构的集合。通过在有无模拟脂质双层的疏水势的真空中对每个集合的代表性成员进行长时间尺度的分子动力学模拟,研究S6和M2随时间的波动。根据S6和M2中扭结的结构基础以及柔性螺旋作为“分子旋转器”的假定功能作用对结果进行了讨论。