Laboratory Architecture et Fonction des Macromolécules Biologiques (AFMB), UMR 7257, Centre National de la Recherche Scientifique (CNRS), Aix Marseille University, CEDEX 9, 13288 Marseille, France.
Biomolecules. 2023 Feb 11;13(2):354. doi: 10.3390/biom13020354.
The split-green fluorescent protein (GFP) reassembly assay is a well-established approach to study protein-protein interactions (PPIs). In this assay, when two interacting proteins X and Y, respectively fused to residues 1-157 and to residues 158-237 of GFP, are co-expressed in , the two GFP halves are brought to sufficient proximity to reassociate and fold to recreate the functional GFP. At constant protein expression level, the intensity of fluorescence produced by the bacteria is proportional to the binding affinity of X to Y. We hypothesized that adding a third partner (Z) endowed with an affinity for either X or Y would lead to an in vivo competition assay. We report here the different steps of the set-up of this competition assay, and define the experimental conditions required to obtained reliable results. Results show that this competition assay is a potentially interesting tool for screening libraries of binding inhibitors, Z being either a protein or a chemical reagent.
分裂绿色荧光蛋白(GFP)重组测定法是一种研究蛋白质-蛋白质相互作用(PPIs)的成熟方法。在该测定法中,当分别融合到 GFP 的残基 1-157 和残基 158-237 的两个相互作用的蛋白质 X 和 Y 在共表达时,两个 GFP 半体被带到足够接近的距离以重新组合并折叠以重新创建功能性 GFP。在恒定的蛋白质表达水平下,细菌产生的荧光强度与 X 与 Y 的结合亲和力成正比。我们假设添加第三个伴侣(Z),其对 X 或 Y 具有亲和力,将导致体内竞争测定法。我们在此报告了建立这种竞争测定法的不同步骤,并定义了获得可靠结果所需的实验条件。结果表明,这种竞争测定法是筛选结合抑制剂文库的一种很有前途的工具,其中 Z 是蛋白质或化学试剂。