Giancola JoLynn B, Okon Aniekan, Li Yanfeng, Strieter Eric R, Raines Ronald T
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Department of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts, USA.
J Pept Sci. 2025 Jun;31(6):e70026. doi: 10.1002/psc.70026.
The proteostasis network involves complex protein signaling cascades. The tagging of proteins with ubiquitin is central to the degradation of cellular proteins, but understanding its exact role in processing proteins is complicated by the complexity and extent of its utilization within cells. Here, we describe the application of a traceless protein delivery strategy to effect the uptake of exogenous ubiquitin into the cytosol of human cells. We find that coadministration of the endosomolytic peptides L17E and, especially, L17ER provides not only cytosolic access to ubiquitin but also its functional incorporation into endogenous proteins. By enabling the study of semisynthetic ubiquitin variants in the human cytosol, this strategy could advance the field of ubiquitin biology.
蛋白质稳态网络涉及复杂的蛋白质信号级联反应。蛋白质的泛素化标记是细胞内蛋白质降解的核心,但由于其在细胞内利用的复杂性和程度,了解其在蛋白质加工中的确切作用变得很复杂。在这里,我们描述了一种无痕蛋白质递送策略的应用,以实现外源性泛素进入人细胞胞质溶胶。我们发现,内体溶解肽L17E,尤其是L17ER的共同给药不仅提供了泛素进入胞质溶胶的途径,还使其功能性地掺入内源性蛋白质中。通过能够在人细胞胞质溶胶中研究半合成泛素变体,该策略可以推动泛素生物学领域的发展。