Gillespie Dirk
Department of Molecular Biophysics and Physiology, Rush University Medical Center, Chicago, Illinois, USA.
Biophys J. 2008 Feb 15;94(4):1169-84. doi: 10.1529/biophysj.107.116798. Epub 2007 Oct 19.
A model of the ryanodine receptor (RyR) calcium channel is used to study the energetics of binding selectivity of Ca(2+) versus monovalent cations. RyR is a calcium-selective channel with a DDDD locus in the selectivity filter, similar to the EEEE locus of the L-type calcium channel. While the affinity of RyR for Ca(2+) is in the millimolar range (as opposed to the micromolar range of the L-type channel), the ease of single-channel measurements compared to L-type and its similar selectivity filter make RyR an excellent candidate for studying calcium selectivity. A Poisson-Nernst-Planck/density functional theory model of RyR is used to calculate the energetics of selectivity. Ca(2+) versus monovalent selectivity is driven by the charge/space competition mechanism in which selectivity arises from a balance of electrostatics and the excluded volume of ions in the crowded selectivity filter. While electrostatic terms dominate the selectivity, the much smaller excluded-volume term also plays a substantial role. In the D4899N and D4938N mutations of RyR that are analyzed, substantial changes in specific components of the chemical potential profiles are found far from the mutation site. These changes result in the significant reduction of Ca(2+) selectivity found in both theory and experiments.
利用兰尼碱受体(RyR)钙通道模型研究Ca(2+)与单价阳离子结合选择性的能量学。RyR是一种钙选择性通道,其选择性过滤器中有一个DDDD位点,类似于L型钙通道的EEEE位点。虽然RyR对Ca(2+)的亲和力处于毫摩尔范围内(与L型通道的微摩尔范围相反),但与L型通道相比,单通道测量更容易,且其选择性过滤器相似,这使得RyR成为研究钙选择性的极佳候选对象。使用RyR的泊松-能斯特-普朗克/密度泛函理论模型来计算选择性的能量学。Ca(2+)与单价阳离子的选择性由电荷/空间竞争机制驱动,其中选择性源于静电作用与拥挤的选择性过滤器中离子的排除体积之间的平衡。虽然静电项主导选择性,但小得多的排除体积项也起着重要作用。在所分析的RyR的D4899N和D4938N突变中,在远离突变位点的化学势分布的特定组分中发现了显著变化。这些变化导致在理论和实验中都发现Ca(2+)选择性显著降低。