Kelly Kristen L, Dalton Shannon R, Wai Rebecca B, Ramchandani Kanika, Xu Rosalind J, Linse Sara, Londergan Casey H
Department of Chemistry , Haverford College , Haverford , Pennsylvania 19041 , United States.
Department of Biochemistry and Structural Biology , Lund University , 221 00 Lund , Sweden.
J Phys Chem A. 2018 Mar 22;122(11):2947-2955. doi: 10.1021/acs.jpca.8b00475. Epub 2018 Mar 9.
Seven native residues on the regulatory protein calmodulin, including three key methionine residues, were replaced (one by one) by the vibrational probe amino acid cyanylated cysteine, which has a unique CN stretching vibration that reports on its local environment. Almost no perturbation was caused by this probe at any of the seven sites, as reported by CD spectra of calcium-bound and apo calmodulin and binding thermodynamics for the formation of a complex between calmodulin and a canonical target peptide from skeletal muscle myosin light chain kinase measured by isothermal titration. The surprising lack of perturbation suggests that this probe group could be applied directly in many protein-protein binding interfaces. The infrared absorption bands for the probe groups reported many dramatic changes in the probes' local environments as CaM went from apo- to calcium-saturated to target peptide-bound conditions, including large frequency shifts and a variety of line shapes from narrow (interpreted as a rigid and invariant local environment) to symmetric to broad and asymmetric (likely from multiple coexisting and dynamically exchanging structures). The fast intrinsic time scale of infrared spectroscopy means that the line shapes report directly on site-specific details of calmodulin's variable structural distribution. Though quantitative interpretation of the probe line shapes depends on a direct connection between simulated ensembles and experimental data that does not yet exist, formation of such a connection to data such as that reported here would provide a new way to evaluate conformational ensembles from data that directly contains the structural distribution. The calmodulin probe sites developed here will also be useful in evaluating the binding mode of calmodulin with many uncharacterized regulatory targets.
调节蛋白钙调蛋白上的七个天然残基,包括三个关键的甲硫氨酸残基,被振动探针氨基酸氰化半胱氨酸逐个取代,该氨基酸具有独特的C≡N伸缩振动,可反映其局部环境。如通过等温滴定量热法测量的钙结合型和脱辅基钙调蛋白的圆二色光谱以及钙调蛋白与骨骼肌肌球蛋白轻链激酶的典型靶肽形成复合物的结合热力学所报道的那样,该探针在这七个位点中的任何一个位点几乎都不会引起扰动。令人惊讶的是缺乏扰动表明该探针基团可以直接应用于许多蛋白质-蛋白质结合界面。当钙调蛋白从脱辅基状态转变为钙饱和状态再到与靶肽结合状态时,探针基团的红外吸收带报告了探针局部环境的许多显著变化,包括大的频率位移和从窄峰(解释为刚性且不变的局部环境)到对称峰再到宽峰和不对称峰(可能来自多种共存且动态交换的结构)的各种线形。红外光谱快速的本征时间尺度意味着线形直接反映了钙调蛋白可变结构分布的位点特异性细节。尽管对探针线形的定量解释依赖于模拟集合与尚未存在的实验数据之间的直接联系,但建立这样一种与本文所报道数据的联系将提供一种从直接包含结构分布的数据中评估构象集合的新方法。此处开发的钙调蛋白探针位点也将有助于评估钙调蛋白与许多未表征的调节靶点的结合模式。