Tracz Michał, Górniak Ireneusz, Szczepaniak Andrzej, Białek Wojciech
Department of Biophysics, Faculty of Biotechnology, University of Wrocław, Joliot-Curie 14a, 50-383 Wrocław, Poland.
Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Int J Mol Sci. 2021 May 27;22(11):5712. doi: 10.3390/ijms22115712.
The SPL2 protein is an E3 ubiquitin ligase of unknown function. It is one of only three types of E3 ligases found in the outer membrane of plant chloroplasts. In this study, we show that the cytosolic fragment of SPL2 binds lanthanide ions, as evidenced by fluorescence measurements and circular dichroism spectroscopy. We also report that SPL2 undergoes conformational changes upon binding of both Ca and La, as evidenced by its partial unfolding. However, these structural rearrangements do not interfere with SPL2 enzymatic activity, as the protein retains its ability to auto-ubiquitinate in vitro. The possible applications of lanthanide-based probes to identify protein interactions in vivo are also discussed. Taken together, the results of this study reveal that the SPL2 protein contains a lanthanide-binding site, showing for the first time that at least some E3 ubiquitin ligases are also capable of binding lanthanide ions.
SPL2蛋白是一种功能未知的E3泛素连接酶。它是在植物叶绿体外膜中发现的仅有的三种E3连接酶类型之一。在本研究中,我们表明SPL2的胞质片段结合镧系离子,荧光测量和圆二色光谱证明了这一点。我们还报告说,在结合Ca和La时,SPL2会发生构象变化,其部分解折叠证明了这一点。然而,这些结构重排并不干扰SPL2的酶活性,因为该蛋白在体外保留了自身泛素化的能力。还讨论了基于镧系元素的探针在体内鉴定蛋白质相互作用的可能应用。综上所述,本研究结果表明SPL2蛋白含有一个镧系元素结合位点,首次表明至少一些E3泛素连接酶也能够结合镧系离子。