Taylor Joshua M, Gerton Kai H, Conboy John C
Department of Chemistry, University of Utah, Salt Lake City, Utah.
Department of Chemistry, University of Utah, Salt Lake City, Utah.
Biophys J. 2025 Apr 15;124(8):1226-1244. doi: 10.1016/j.bpj.2025.02.028. Epub 2025 Mar 6.
Vitamin E (VE) has historically been described as an antioxidant and its roles in radical species scavenging and nutrition are well studied. VE has been proposed to have secondary roles within the membrane but these roles are not as well characterized, with contradictory results emerging throughout the literature. Due to similar structural motifs, comparisons between VE and cholesterol (CHO), another membrane component, have been commonly made. Despite these comparisons showing that phospholipid-CHO and phospholipid-VE interactions may behave similarly, VE's potential influence on phospholipid flip-flop specifically is not as well studied when compared with CHO's influence. Here, we show through the use of sum-frequency vibrational spectroscopy that VE at both biological (0.5-1.5 mol %) and supraphysiological (2.5-5 mol %) concentrations shows similar characteristics to that of CHO in its ability to induce alkyl chain ordering of phospholipids within planar supported lipid bilayers of the saturated lipid 1,2-dipalmitoyl-sn-glycero-3-phosphocholine. In addition to chain ordering, the introduction of VE accelerates phospholipid flip-flop by approximately three times (0.5-2.5 mol %) with rates approaching an order-of-magnitude increase (5 mol %) at high VE content. The increase in phospholipid flip-flop rates is attributed to the decrease in the molar compression modulus of the membrane. These results suggest that VE influences the ordering and compressibility of the membrane similar to CHO.
维生素E(VE)在历史上一直被描述为一种抗氧化剂,其在清除自由基和营养方面的作用已得到充分研究。有人提出VE在膜内具有次要作用,但这些作用尚未得到很好的表征,整个文献中出现了相互矛盾的结果。由于结构基序相似,VE与膜的另一种成分胆固醇(CHO)之间经常进行比较。尽管这些比较表明磷脂-CHO和磷脂-VE相互作用可能表现相似,但与CHO的影响相比,VE对磷脂翻转的潜在影响尚未得到很好的研究。在这里,我们通过和频振动光谱表明,在生物浓度(0.5-1.5摩尔%)和超生理浓度(2.5-5摩尔%)下,VE在诱导饱和脂质1,2-二棕榈酰-sn-甘油-3-磷酸胆碱的平面支撑脂质双层内磷脂的烷基链有序排列方面与CHO具有相似的特性。除了链有序排列外,VE的引入使磷脂翻转加速了约三倍(0.5-2.5摩尔%),在高VE含量下速率接近一个数量级的增加(5摩尔%)。磷脂翻转速率的增加归因于膜的摩尔压缩模量的降低。这些结果表明,VE对膜的有序排列和可压缩性的影响与CHO相似。