Institute of Cytology of the Russian Academy of Sciences, Laboratory of Structural Dynamics, Stability and Folding of Proteins, Tikhoretsky av. 4, 194064 St. Petersburg, Russia.
Saint Petersburg State University, Universitetskaya nab. 7/9, 199034 St. Petersburg, Russia.
Int J Mol Sci. 2017 Sep 19;18(9):2008. doi: 10.3390/ijms18092008.
The ability of d-glucose/d-galactose-binding protein (GGBP) to reversibly interact with its ligands, glucose and galactose, makes this protein an attractive candidate for sensing elements of glucose biosensors. This potential is largely responsible for attracting researchers to study the conformational properties of this protein. Previously, we showed that an increase in the fluorescence intensity of the fluorescent dye 6-bromoacetyl-2-dimetylaminonaphtalene (BADAN) is linked to the holo-form of the GGBP/H152C mutant in solutions containing sub-denaturing concentrations of guanidine hydrochloride (GdnHCl). It was hypothesized that low GdnHCl concentrations might lead to compaction of the protein, thereby facilitating ligand binding. In this work, we utilize BADAN fluorescence spectroscopy, intrinsic protein UV fluorescence spectroscopy, and isothermal titration calorimetry (ITC) to show that the sub-denaturing GdnHCl concentrations possess osmolyte-like stabilizing effects on the structural dynamics, conformational stability, and functional activity of GGBP/H152C and the wild type of this protein (wtGGBP). Our data are consistent with the model where low GdnHCl concentrations promote a shift in the dynamic distribution of the protein molecules toward a conformational ensemble enriched in molecules with a tighter structure and a more closed conformation. This promotes the increase in the configurational complementarity between the protein and glucose molecules that leads to the increase in glucose affinity in both GGBP/H152C and wtGGBP.
d-葡萄糖/d-半乳糖结合蛋白(GGBP)与配体葡萄糖和半乳糖可逆相互作用的能力使其成为葡萄糖生物传感器传感元件的有吸引力的候选物。这种潜力在很大程度上吸引了研究人员研究该蛋白的构象特性。以前,我们表明,在含有亚变性浓度盐酸胍(GdnHCl)的溶液中,荧光染料 6-溴乙酰基-2-二甲氨基萘(BADAN)的荧光强度增加与 GGBP/H152C 突变体的全酶形式有关。据推测,低 GdnHCl 浓度可能导致蛋白质紧缩,从而促进配体结合。在这项工作中,我们利用 BADAN 荧光光谱法、蛋白质内源紫外荧光光谱法和等温热滴定法(ITC)表明,亚变性 GdnHCl 浓度对 GGBP/H152C 和该蛋白的野生型(wtGGBP)的结构动力学、构象稳定性和功能活性具有类似渗透剂的稳定作用。我们的数据与以下模型一致,即低 GdnHCl 浓度促使蛋白质分子的动态分布向富含具有更紧密结构和更封闭构象的分子的构象集合发生转移。这促进了蛋白质和葡萄糖分子之间构象互补性的增加,从而导致 GGBP/H152C 和 wtGGBP 中葡萄糖亲和力的增加。