Department of Biological Sciences, Delaware State University, Dover, Delaware, USA.
Department of Chemistry, Colorado State University, Fort Collins, Colorado, USA.
Protein Sci. 2024 Apr;33(4):e4919. doi: 10.1002/pro.4919.
Protein-protein interactions (PPIs) are central to many cellular processes, and the identification of novel PPIs is a critical step in the discovery of protein therapeutics. Simple methods to identify naturally existing or laboratory evolved PPIs are therefore valuable research tools. We have developed a facile selection that links PPI-dependent β-lactamase recruitment on the surface of Escherichia coli with resistance to ampicillin. Bacteria displaying a protein that forms a complex with a specific protein-β-lactamase fusion are protected from ampicillin-dependent cell death. In contrast, bacteria that do not recruit β-lactamase to the cell surface are killed by ampicillin. Given its simplicity and tunability, we anticipate this selection will be a valuable addition to the palette of methods for illuminating and interrogating PPIs.
蛋白质-蛋白质相互作用(PPIs)是许多细胞过程的核心,鉴定新的 PPI 是发现蛋白质治疗药物的关键步骤。因此,简单的方法来识别自然存在或实验室进化的 PPIs 是有价值的研究工具。我们开发了一种简单的选择方法,将依赖于 PPI 的β-内酰胺酶在大肠杆菌表面的募集与氨苄青霉素抗性联系起来。在表面展示与特定蛋白-β-内酰胺酶融合体形成复合物的蛋白质的细菌可以免受氨苄青霉素依赖性细胞死亡的影响。相比之下,不能将β-内酰胺酶募集到细胞表面的细菌会被氨苄青霉素杀死。鉴于其简单性和可调节性,我们预计这种选择将是阐明和研究 PPI 的方法的一个有价值的补充。