Ittig Simon J, Schmutz Christoph, Kasper Christoph A, Amstutz Marlise, Schmidt Alexander, Sauteur Loïc, Vigano M Alessandra, Low Shyan Huey, Affolter Markus, Cornelis Guy R, Nigg Erich A, Arrieumerlou Cécile
Biozentrum, University of Basel, 4056 Basel, Switzerland.
Research Unit in Biology of Microorganisms, Department of Biology, University of Namur, 5000 Namur, Belgium.
J Cell Biol. 2015 Nov 23;211(4):913-31. doi: 10.1083/jcb.201502074.
Methods enabling the delivery of proteins into eukaryotic cells are essential to address protein functions. Here we propose broad applications to cell biology for a protein delivery tool based on bacterial type III secretion (T3S). We show that bacterial, viral, and human proteins, fused to the N-terminal fragment of the Yersinia enterocolitica T3S substrate YopE, are effectively delivered into target cells in a fast and controllable manner via the injectisome of extracellular bacteria. This method enables functional interaction studies by the simultaneous injection of multiple proteins and allows the targeting of proteins to different subcellular locations by use of nanobody-fusion proteins. After delivery, proteins can be freed from the YopE fragment by a T3S-translocated viral protease or fusion to ubiquitin and cleavage by endogenous ubiquitin proteases. Finally, we show that this delivery tool is suitable to inject proteins in living animals and combine it with phosphoproteomics to characterize the systems-level impact of proapoptotic human truncated BID on the cellular network.
能够将蛋白质递送至真核细胞的方法对于研究蛋白质功能至关重要。在此,我们提出基于细菌III型分泌(T3S)的蛋白质递送工具在细胞生物学中的广泛应用。我们表明,与小肠结肠炎耶尔森菌T3S底物YopE的N端片段融合的细菌、病毒和人类蛋白质,可通过细胞外细菌的注射体以快速且可控的方式有效地递送至靶细胞。该方法能够通过同时注射多种蛋白质进行功能相互作用研究,并允许通过使用纳米抗体融合蛋白将蛋白质靶向到不同的亚细胞位置。递送后,蛋白质可通过T3S易位的病毒蛋白酶从YopE片段中释放出来,或与泛素融合并通过内源性泛素蛋白酶进行切割。最后,我们表明这种递送工具适用于在活体动物中注射蛋白质,并将其与磷酸蛋白质组学相结合,以表征促凋亡人类截短型BID对细胞网络的系统水平影响。