Department of Physics, Syracuse University , 201 Physics Building, Syracuse, New York 13244-1130, United States.
Structural Biology, Biochemistry, and Biophysics Program, Syracuse University , 111 College Place, Syracuse, New York 13244-4100, United States.
Anal Chem. 2017 Aug 1;89(15):8013-8020. doi: 10.1021/acs.analchem.7b01339. Epub 2017 Jul 10.
Understanding how membrane proteins interact with detergents is of fundamental and practical significance in structural and chemical biology as well as in nanobiotechnology. Current methods for inspecting protein-detergent complex (PDC) interfaces require high concentrations of protein and are of low throughput. Here, we describe a scalable, spectroscopic approach that uses nanomolar protein concentrations in native solutions. This approach, which is based on steady-state fluorescence polarization (FP) spectroscopy, kinetically resolves the dissociation of detergents from membrane proteins and protein unfolding. For satisfactorily solubilizing detergents, at concentrations much greater than the critical micelle concentration (CMC), the fluorescence anisotropy was independent of detergent concentration. In contrast, at detergent concentrations comparable with or below the CMC, the anisotropy readout underwent a time-dependent decrease, showing a specific and sensitive protein unfolding signature. Functionally reconstituted membrane proteins into a bilayer membrane confirmed predictions made by these FP-based determinations with respect to varying refolding conditions. From a practical point of view, this 96-well analytical approach will facilitate a massively parallel assessment of the PDC interfacial interactions under a fairly broad range of micellar and environmental conditions. We expect that these studies will potentially accelerate research in membrane proteins pertaining to their extraction, solubilization, stabilization, and crystallization, as well as reconstitution into bilayer membranes.
理解膜蛋白与去污剂的相互作用在结构和化学生物学以及纳米生物技术中具有基础和实际意义。目前检查蛋白质-去污剂复合物(PDC)界面的方法需要高浓度的蛋白质,并且通量较低。在这里,我们描述了一种可扩展的、基于光谱的方法,该方法在天然溶液中使用纳摩尔浓度的蛋白质。这种方法基于稳态荧光偏振(FP)光谱,能够动态解析去污剂从膜蛋白上的解离和蛋白展开。对于令人满意地溶解去污剂,在远远高于临界胶束浓度(CMC)的浓度下,荧光各向异性与去污剂浓度无关。相比之下,在与 CMC 相当或低于 CMC 的去污剂浓度下,各向异性读数会随时间下降,显示出特定且灵敏的蛋白展开特征。将功能重建的膜蛋白嵌入双层膜中,证实了这些基于 FP 的测定对不同重折叠条件的预测。从实际的角度来看,这种 96 孔分析方法将有助于在相当广泛的胶束和环境条件下大规模平行评估 PDC 界面相互作用。我们预计,这些研究将有可能加速与膜蛋白相关的提取、溶解、稳定和结晶以及双层膜重建的研究。