Jain Bhawik K, Mansueto Alexander J, Graham Todd R
Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA.
Methods Mol Biol. 2025;2888:133-145. doi: 10.1007/978-1-0716-4318-1_10.
Phospholipid flippases in the P4-ATPase family are essential for establishing membrane asymmetry. These ATP-powered pumps translocate specific lipids from the exofacial leaflet to the cytosolic leaflet of the plasma membrane, thereby concentrating substrate lipids, such as phosphatidylserine, in the cytosolic leaflet while non-substrate lipids populate the exofacial leaflet. Here, we describe a method for measuring P4-ATPase transport activity in the yeast plasma membrane by using flow cytometry to quantify the uptake of lipids derivatized with a fluorescent [7-nitro-2-1,3-benzoxadiazol-4-yl)amino] (NBD) group on a short (C6) fatty acyl chain. The NBD-lipid uptake assay quantitatively measures P4-ATPase transport activity and substrate selectivity in the native membrane environment.
P4-ATPase家族中的磷脂翻转酶对于建立膜不对称性至关重要。这些由ATP驱动的泵将特定脂质从质膜的细胞外侧小叶转运至胞质小叶,从而使底物脂质(如磷脂酰丝氨酸)在胞质小叶中富集,而非底物脂质则分布在细胞外侧小叶。在此,我们描述了一种通过流式细胞术测量酵母质膜中P4-ATPase转运活性的方法,以量化带有短(C6)脂肪酰链的荧光[7-硝基-2-1,3-苯并恶二唑-4-基)氨基](NBD)基团衍生化的脂质的摄取。NBD-脂质摄取测定法定量测量天然膜环境中P4-ATPase的转运活性和底物选择性。