European Molecular Biology Laboratory (EMBL), Cell Biology & Biophysics Unit, Meyerhofstr. 1, 69117, Heidelberg, Germany.
Faculty of Biosciences, Collaboration for Joint Ph.D. Degree between EMBL and Heidelberg University, 69117, Heidelberg, Germany.
Angew Chem Int Ed Engl. 2021 Sep 1;60(36):19759-19765. doi: 10.1002/anie.202103599. Epub 2021 Jul 26.
We synthesized the first multifunctionalized phosphoinositide polyphosphate derivatives featuring a photo-removable protecting group ("cage"), a photo-crosslinkable diazirine group, and a terminal alkyne group useful for click chemistry. We demonstrate that the lipid derivatives readily enter cells. After photo-crosslinking, cell fixation and fluorescent tagging via click chemistry, we determined the intracellular location of the lipid derivatives before and after uncaging of the lipids. We find that there is rapid trafficking of PI(3,4)P and PI(3,4,5)P derivatives to the plasma membrane, opening the intriguing possibility that there is active transport of these lipids involved. We employed the photo-crosslinking and click chemistry functions to analyze the proteome of PI(3,4,5)P -binding proteins. From the latter, we validated by RNAi that the putative lipid binding proteins ATP11A and MPP6 are involved in the transport of PI(3,4,5)P to the plasma membrane.
我们合成了首批具有光解保护基团(“笼”)、光交联叠氮基团和末端炔基的多功能化磷酸肌醇多磷酸盐衍生物,这些基团可用于点击化学。我们证明了这些脂质衍生物很容易进入细胞。在光交联、细胞固定和通过点击化学进行荧光标记后,我们在脂质去笼化前后确定了脂质衍生物在细胞内的位置。我们发现 PI(3,4)P 和 PI(3,4,5)P 衍生物迅速转运到质膜,这提出了一个有趣的可能性,即这些脂质的主动转运可能涉及其中。我们利用光交联和点击化学功能来分析 PI(3,4,5)P 结合蛋白的蛋白质组。通过后者,我们通过 RNAi 验证了假定的脂质结合蛋白 ATP11A 和 MPP6 参与了 PI(3,4,5)P 向质膜的转运。