Department of Chemical & Biomolecular Engineering, University of Nebraska-Lincoln, Lincoln, Nebraska, 68588, USA.
Department of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska, 68588, USA.
Nat Commun. 2020 Sep 24;11(1):4820. doi: 10.1038/s41467-020-18629-9.
Protein tyrosine O-sulfation (PTS) plays a crucial role in extracellular biomolecular interactions that dictate various cellular processes. It also involves in the development of many human diseases. Regardless of recent progress, our current understanding of PTS is still in its infancy. To promote and facilitate relevant studies, a generally applicable method is needed to enable efficient expression of sulfoproteins with defined sulfation sites in live mammalian cells. Here we report the engineering, in vitro biochemical characterization, structural study, and in vivo functional verification of a tyrosyl-tRNA synthetase mutant for the genetic encoding of sulfotyrosine in mammalian cells. We further apply this chemical biology tool to cell-based studies on the role of a sulfation site in the activation of chemokine receptor CXCR4 by its ligand. Our work will not only facilitate cellular studies of PTS, but also paves the way for economical production of sulfated proteins as therapeutic agents in mammalian systems.
蛋白质酪氨酸 O-硫酸化 (PTS) 在决定各种细胞过程的细胞外生物分子相互作用中起着至关重要的作用。它还涉及许多人类疾病的发展。尽管最近取得了进展,但我们对 PTS 的理解仍处于起步阶段。为了促进和便利相关研究,需要一种通用的方法来实现在活哺乳动物细胞中有效表达具有定义的硫酸化位点的硫酸化蛋白。在这里,我们报告了一种用于在哺乳动物细胞中遗传编码硫酸酪氨酸的酪氨酸 tRNA 合成酶突变体的工程设计、体外生化特性分析、结构研究和体内功能验证。我们进一步将这个化学生物学工具应用于基于细胞的研究,以研究硫酸化位点在其配体激活趋化因子受体 CXCR4 中的作用。我们的工作不仅将促进 PTS 的细胞研究,而且还为在哺乳动物系统中作为治疗剂经济地生产硫酸化蛋白铺平了道路。