Kamaloo Elaheh, Camesano Terri A, Nagarajan Ramanathan
Department of Chemical Engineering, Worcester Polytechnic Institute, Worcester, MA 01609, USA.
US Army Combat Capabilities Development Command Soldier Center, Natick, MA 01760, USA.
Biomolecules. 2025 Mar 2;15(3):362. doi: 10.3390/biom15030362.
Supported lipid bilayers (SLBs) that model neuronal membranes are needed to explore the role of membrane lipids in the misfolding and aggregation of amyloid proteins associated with neurodegenerative diseases, including Parkinson's and Alzheimer's disease. The neuronal membranes include not only phospholipids, but also significant amounts of cholesterol, sphingomyelin, and gangliosides, which are critical to its biological function. In this study, we explored the conditions for the formation of an SLB, for the five-component lipid mixture composed of zwitterionic 1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC), anionic 1,2-dioleoyl- sn-glycero-3-phospho-L-serine (DOPS), nonionic cholesterol (Chol), zwitterionic sphingomyelin (SM), and anionic ganglioside (GM), using the quartz crystal microbalance with dissipation monitoring (QCM-D) technique, by varying experimental parameters such as pH, buffer type, temperature, vesicle size, and osmotic stress. SLB formation from this multicomponent lipid system was found challenging because the vesicles adsorbed intact on the quartz crystal and failed to rupture. For most of the variables tested, other than osmotic stress, we found no or only partial vesicle rupture leading to either a supported layer of vesicles or a partial SLB that included unruptured vesicles. When osmotic stress was applied to the vesicles already adsorbed on the surface, by having a different salt concentration in the rinse buffer that follows vesicle flow compared to that of the dilution buffer during vesicle flow and adsorption, vesicle rupture increased, but it remained incomplete. In contrast, when osmotic stress was applied during vesicle flow and adsorption on the surface, by having different salt concentrations in the dilution buffer in which vesicles flowed compared to the hydration buffer in which vesicles were prepared, complete vesicle rupture and successful formation of a rigid SLB was demonstrated. The robustness of this approach to form SLBs by applying osmotic stress during vesicle adsorption was found to be independent of the number of lipid components, as shown by SLB formation from the 1-, 2-, 3-, 4-, and 5-component lipid systems.
为了探究膜脂在与神经退行性疾病(包括帕金森病和阿尔茨海默病)相关的淀粉样蛋白错误折叠和聚集过程中的作用,需要构建模拟神经元膜的支撑脂质双层(SLB)。神经元膜不仅包含磷脂,还含有大量对其生物学功能至关重要的胆固醇、鞘磷脂和神经节苷脂。在本研究中,我们使用带耗散监测的石英晶体微天平(QCM-D)技术,通过改变pH、缓冲液类型、温度、囊泡大小和渗透压等实验参数,探索了由两性离子1,2-二油酰-sn-甘油-3-磷酸胆碱(DOPC)、阴离子1,2-二油酰-sn-甘油-3-磷酸-L-丝氨酸(DOPS)、非离子胆固醇(Chol)、两性离子鞘磷脂(SM)和阴离子神经节苷脂(GM)组成的五组分脂质混合物形成SLB的条件。发现从这种多组分脂质系统形成SLB具有挑战性,因为囊泡完整地吸附在石英晶体上且未破裂。对于测试的大多数变量(渗透压除外),我们发现没有囊泡破裂或只有部分囊泡破裂,导致形成囊泡支撑层或包含未破裂囊泡的部分SLB。当对已经吸附在表面的囊泡施加渗透压时,通过使囊泡流动后的冲洗缓冲液中的盐浓度与囊泡流动和吸附期间的稀释缓冲液中的盐浓度不同,囊泡破裂增加,但仍不完全。相比之下,当在囊泡在表面流动和吸附期间施加渗透压时,通过使囊泡流动的稀释缓冲液中的盐浓度与制备囊泡的水化缓冲液中的盐浓度不同,证明了囊泡完全破裂并成功形成刚性SLB。通过在囊泡吸附期间施加渗透压来形成SLB的这种方法的稳健性被发现与脂质成分的数量无关,由1、2、3、4和5组分脂质系统形成SLB证明了这一点。