Global Health Institute, Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Laboratory of Computational Systems Biotechnology, Faculty of Basic Sciences, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Elife. 2017 Aug 15;6:e27826. doi: 10.7554/eLife.27826.
S-Palmitoylation is the only reversible post-translational lipid modification. Knowledge about the DHHC palmitoyltransferase family is still limited. Here we show that human ZDHHC6, which modifies key proteins of the endoplasmic reticulum, is controlled by an upstream palmitoyltransferase, ZDHHC16, revealing the first palmitoylation cascade. The combination of site specific mutagenesis of the three ZDHHC6 palmitoylation sites, experimental determination of kinetic parameters and data-driven mathematical modelling allowed us to obtain detailed information on the eight differentially palmitoylated ZDHHC6 species. We found that species rapidly interconvert through the action of ZDHHC16 and the Acyl Protein Thioesterase APT2, that each species varies in terms of turnover rate and activity, altogether allowing the cell to robustly tune its ZDHHC6 activity.
S-棕榈酰化是唯一一种可逆转的翻译后脂质修饰。DHHC 棕榈酰转移酶家族的知识仍然有限。在这里,我们展示了修饰内质网关键蛋白的人 ZDHHC6 受上游棕榈酰转移酶 ZDHHC16 控制,揭示了第一个棕榈酰化级联。对 ZDHHC6 的三个棕榈酰化位点进行定点突变、实验确定动力学参数和数据驱动的数学建模相结合,使我们能够获得关于八种不同棕榈酰化 ZDHHC6 物种的详细信息。我们发现,通过 ZDHHC16 和酰基辅酶 A 蛋白硫酯酶 APT2 的作用,物种迅速相互转化,每种物种的周转率和活性都不同,这使得细胞能够稳健地调节其 ZDHHC6 活性。