Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
J Phys Chem B. 2022 Oct 6;126(39):7651-7663. doi: 10.1021/acs.jpcb.2c04039. Epub 2022 Sep 21.
The influence of ytterbium ions (Yb), a commonly used paramagnetic NMR chemical shift reagent, on the physical properties and flip-flop kinetics of dipalmitoylphosphatidylcholine (DPPC) planar supported lipid bilayers (PSLBs) was investigated. Langmuir isotherm studies revealed that Yb interacts strongly with the phosphate headgroup of DPPC, evidenced by the increases in shear and compression moduli. Using sum-frequency vibrational spectroscopy, changes in the acyl chain ordering and phase transition temperature were also observed, consistent with Yb interacting with the phosphate headgroup of DPPC. The changes in the physical properties of the membrane were also observed to be concentration dependent, with more pronounced modification observed at low (50 μM) Yb concentrations compared to 6.5 mM Tb, suggesting a cross-linking mechanism between adjacent DPPC lipids. Additionally, the changes in membrane packing and phase transition temperatures in the presence of Tris buffer suggested that a putative Yb(Tris) complex forms that coordinates to the PC headgroup. The kinetics of DPPC flip-flop in the gel and liquid crystalline (lc) phases were substantially inhibited in the presence of Yb, regardless of the Yb concentration. Analysis of the flip-flop kinetics under the framework of transition state theory revealed that the free energy barrier to flip-flop in both the gel and lc phases was substantial increased over a pure DPPC membrane. In the gel phase, the trend in the free energy barrier appeared to follow the trend in the shear moduli, suggesting that the Yb-DPPC headgroup interaction was driving the increase in the activation free energy barrier. In the lc phase, activation free energies of DPPC flip-flop in the presence of 50 μM or 6.5 mM Yb were found to mirror the free energies of TEMPO-DPPC flip-flop, leading to the conclusion that the strong interaction between Yb and the PC headgroup was essentially manifested as a headgroup charge modification. These studies illustrate that the presence of the lanthanide Yb results in significant modification to the lipid membrane physical properties and, more importantly, results in a pronounced inhibition of native lipid flip-flop.
镱离子(Yb)是一种常用的顺磁核磁化学位移试剂,研究了其对二棕榈酰磷脂酰胆碱(DPPC)平面支撑脂质双层(PSLB)的物理性质和翻转动力学的影响。Langmuir 等温线研究表明,Yb 与 DPPC 的磷酸头部基团强烈相互作用,这表现为剪切和压缩模量的增加。利用和频振动光谱,也观察到酰基链有序性和相变温度的变化,这与 Yb 与 DPPC 的磷酸头部基团相互作用一致。还观察到膜的物理性质随浓度变化而变化,在低浓度(50 μM)Yb 时观察到更明显的修饰,与 6.5 mM Tb 相比,这表明相邻 DPPC 脂质之间存在交联机制。此外,在 Tris 缓冲液存在的情况下,膜包装和相变温度的变化表明形成了一种假定的 Yb(Tris)配合物,该配合物与 PC 头部基团配位。在存在 Yb 的情况下,DPPC 在凝胶和液晶(lc)相中的翻转动力学被大大抑制,而与 Yb 浓度无关。根据过渡态理论对翻转动力学的分析表明,凝胶和 lc 相中的 DPPC 翻转自由能垒都大大增加,超过了纯 DPPC 膜。在凝胶相中,自由能垒的趋势似乎遵循剪切模量的趋势,这表明 Yb-DPPC 头部基团相互作用是导致激活自由能垒增加的原因。在 lc 相中,发现存在 50 μM 或 6.5 mM Yb 时 DPPC 翻转的激活自由能与 TEMPO-DPPC 翻转的自由能相似,这导致了这样的结论,即 Yb 和 PC 头部基团之间的强相互作用本质上表现为头部基团电荷修饰。这些研究表明,镧系元素 Yb 的存在会导致脂质膜物理性质的显著变化,更重要的是,会导致天然脂质翻转的明显抑制。