Molecular Biophysics Program and Department of Biochemistry, University of Colorado, Boulder, CO, 80309-0596, United States.
Molecular Biophysics Program and Department of Biochemistry, University of Colorado, Boulder, CO, 80309-0596, United States.
Anal Biochem. 2021 Apr 1;618:114066. doi: 10.1016/j.ab.2020.114066. Epub 2021 Jan 22.
The many members of the Ras superfamily are small GTPases that serve as molecular switches. These proteins bind the guanine nucleotides GTP and GDP with picomolar affinities, thereby stabilizing on- and off-signaling states, respectively. Quantitative in vitro Ras studies require accurate determination of total protein, its fractional occupancy with guanine nucleotide, and spectroscopic purity. Yet the high nucleotide affinity of Ras and the overlapping UV spectra of the protein and bound nucleotide make such determinations challenging. Here we describe a generalizable UV spectral deconvolution method to analyze the total protein concentration, total nucleotide stoichiometry, and purity of Ras complexes.
Ras 超家族的众多成员都是小 GTP 酶,它们充当分子开关。这些蛋白质以皮摩尔亲和力结合鸟嘌呤核苷酸 GTP 和 GDP,从而分别稳定信号开启和关闭状态。定量的体外 Ras 研究需要准确测定总蛋白、其与鸟嘌呤核苷酸的分数占有率以及光谱纯度。然而,Ras 的高核苷酸亲和力以及蛋白和结合核苷酸的重叠紫外光谱使得这些测定具有挑战性。在这里,我们描述了一种可推广的紫外光谱解卷积方法,用于分析 Ras 复合物的总蛋白浓度、总核苷酸化学计量和纯度。