Whiting Rose, Stanton Sevio, Kucheriava Maryna, Smith Aviana R, Pitts Matt, Robertson Daniel, Kammer Jacob, Li Zhiyu, Fologea Daniel
Department of Physics, Boise State University, Boise, ID 83725, USA.
Biomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.
Membranes (Basel). 2023 Jun 25;13(7):620. doi: 10.3390/membranes13070620.
Lipid ordering in cell membranes has been increasingly recognized as an important factor in establishing and regulating a large variety of biological functions. Multiple investigations into lipid organization focused on assessing ordering from temperature-induced phase transitions, which are often well outside the physiological range. However, particular stresses elicited by environmental factors, such as hypo-osmotic stress or protein insertion into membranes, with respect to changes in lipid status and ordering at constant temperature are insufficiently described. To fill these gaps in our knowledge, we exploited the well-established ability of environmentally sensitive membrane probes to detect intramembrane changes at the molecular level. Our steady state fluorescence spectroscopy experiments focused on assessing changes in optical responses of Laurdan and diphenylhexatriene upon exposure of red blood cells to hypo-osmotic stress and pore-forming toxins at room temperature. We verified our utilized experimental systems by a direct comparison of the results with prior reports on artificial membranes and cholesterol-depleted membranes undergoing temperature changes. The significant changes observed in the lipid order after exposure to hypo-osmotic stress or pore-forming toxins resembled phase transitions of lipids in membranes, which we explained by considering the short-range interactions between membrane components and the hydrophobic mismatch between membrane thickness and inserted proteins. Our results suggest that measurements of optical responses from the membrane probes constitute an appropriate method for assessing the status of lipids and phase transitions in target membranes exposed to mechanical stresses or upon the insertion of transmembrane proteins.
细胞膜中的脂质有序排列已日益被视为建立和调节多种生物学功能的重要因素。多项关于脂质组织的研究聚焦于评估温度诱导的相变所导致的有序排列,而这些相变通常处于生理范围之外。然而,对于环境因素引发的特定应激,如低渗应激或蛋白质插入膜中,在恒定温度下脂质状态和有序排列的变化却描述不足。为填补这些知识空白,我们利用了对环境敏感的膜探针在分子水平检测膜内变化的成熟能力。我们的稳态荧光光谱实验着重评估了在室温下红细胞暴露于低渗应激和孔形成毒素时,劳丹(Laurdan)和二苯基己三烯(diphenylhexatriene)的光学响应变化。我们通过将结果与先前关于经历温度变化的人工膜和胆固醇耗尽膜的报告进行直接比较,验证了我们所使用的实验系统。在暴露于低渗应激或孔形成毒素后观察到的脂质有序排列的显著变化类似于膜中脂质的相变,我们通过考虑膜成分之间的短程相互作用以及膜厚度与插入蛋白质之间的疏水不匹配来解释这一现象。我们的结果表明,测量膜探针的光学响应是评估暴露于机械应力或跨膜蛋白插入时靶膜中脂质状态和相变的一种合适方法。