Instituto Biofisika (CSIC, UPV/EHU), Campus Universitario, 48940 Leioa, Spain.
Departamento de Bioquímica, Universidad del País Vasco, 48940 Leioa, Spain.
Int J Mol Sci. 2020 Apr 10;21(7):2643. doi: 10.3390/ijms21072643.
This study was aimed at preparing and characterizing plasma membranes (PM) from Chinese Hamster Ovary (CHO) cells. Two methods of PM preparation were applied, one based on adhering cells to a poly-lysine-coated surface, followed by hypotonic lysis and removal of intracellular components, so that PM patches remain adhered to each other, and a second one consisting of bleb induction in cells, followed by separation of giant plasma membrane vesicles (GPMV). Both methods gave rise to PM in sufficient amounts to allow biophysical and biochemical characterization. Laurdan generalized polarization was used to measure molecular order in membranes, PM preparations were clearly more ordered than the average cell membranes (GP ≈0.450 vs. ≈0.20 respectively). Atomic force microscopy was used in the force spectroscopy mode to measure breakthrough forces of PM, both PM preparations provided values in the 4-6 nN range, while the corresponding value for whole cell lipid extracts was ≈2 nN. Lipidomic analysis of the PM preparations revealed that, as compared to the average cell membranes, PM were enriched in phospholipids containing 30-32 C atoms in their acyl chains but were relatively poor in those containing 34-40 C atoms. PM contained more saturated and less polyunsaturated fatty acids than the average cell membranes. Blebs (GPMV) and patches were very similar in their lipid composition, except that blebs contained four-fold the amount of cholesterol of patches (≈23 vs. ≈6 mol% total membrane lipids) while the average cell lipids contained 3 mol%. The differences in lipid composition are in agreement with the observed variations in physical properties between PM and whole cell membranes.
本研究旨在制备和表征中国仓鼠卵巢(CHO)细胞的质膜(PM)。应用了两种 PM 制备方法,一种方法基于将细胞附着在聚赖氨酸涂层表面上,然后通过低渗裂解去除细胞内成分,从而使 PM 斑块彼此粘附,另一种方法由细胞中的泡囊诱导组成,然后分离巨大质膜囊泡(GPMV)。这两种方法都产生了足够数量的 PM,允许进行生物物理和生化特性分析。使用 Laurdan 普遍极化来测量膜中的分子有序性,PM 制剂明显比普通细胞膜更有序(GP ≈0.450 与 ≈0.20 分别)。原子力显微镜用于力谱模式测量 PM 的突破力,两种 PM 制剂都提供了 4-6 nN 的范围内的值,而相应的全细胞脂质提取物的值约为 2 nN。PM 制剂的脂质组学分析表明,与普通细胞膜相比,PM 富含含有 30-32 个碳原子的酰基链的磷脂,但相对缺乏含有 34-40 个碳原子的磷脂。PM 比普通细胞膜含有更多的饱和脂肪酸和较少的多不饱和脂肪酸。泡囊(GPMV)和斑块在脂质组成上非常相似,除了泡囊中含有四倍于斑块的胆固醇含量(≈23 与 ≈6 摩尔%总膜脂质),而普通细胞脂质含有 3 摩尔%。脂质组成的差异与 PM 和全细胞膜之间观察到的物理性质变化一致。