Foo Sherman, Oliferenko Snezhana
Randall Centre for Cell and Molecular Biophysics, School of Basic and Medical Biosciences, King's College London, London, UK.
The Francis Crick Institute, London, UK.
Methods Mol Biol. 2025;2958:99-118. doi: 10.1007/978-1-0716-4714-1_7.
Although the outer membrane of the nuclear envelope is continuous with the endoplasmic reticulum, temporally regulated and functionally significant differences in membrane lipid composition may exist between the two nuclear membranes and between the outer nuclear membrane and the endoplasmic reticulum. Biochemical approaches to probing lipid composition are challenged when lipid dynamics must be analyzed with fine spatiotemporal resolution, for instance, within the cell cycle of a single cell. Here we describe a method to probe the distribution of phosphatidic acid and diacylglycerol, two interconvertible biosynthetic precursors for other membrane glycerophospholipids, in living cells of the model fission yeast Schizosaccharomyces pombe. We show how genetically encoded fluorescent biosensors can be constructed and optimized and present a protocol to probe and quantify phosphatidic acid and diacylglycerol levels specifically at the inner nuclear membrane.
尽管核膜的外膜与内质网相连,但两层核膜之间以及外核膜与内质网之间可能存在时间调控且功能上重要的膜脂成分差异。当必须以精细的时空分辨率分析脂质动态时,例如在单个细胞的细胞周期内,探测脂质成分的生化方法面临挑战。在这里,我们描述了一种在模式裂殖酵母粟酒裂殖酵母的活细胞中探测磷脂酸和二酰基甘油(其他膜甘油磷脂的两种可相互转化的生物合成前体)分布的方法。我们展示了如何构建和优化基因编码的荧光生物传感器,并给出了一个专门探测和量化内核膜处磷脂酸和二酰基甘油水平的方案。