Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal; Large Scale Structures Group, Institut Laue-Langevin, 38042 Cedex 9, Grenoble, France.
Large Scale Structures Group, Institut Laue-Langevin, 38042 Cedex 9, Grenoble, France; Departamento de Química Física, Universidad Complutense de Madrid, 28040, Madrid, Spain.
Colloids Surf B Biointerfaces. 2023 Jul;227:113341. doi: 10.1016/j.colsurfb.2023.113341. Epub 2023 May 10.
The combination of in vitro models of biological membranes based on solid-supported lipid bilayers (SLBs) and of surface sensitive techniques, such as neutron reflectometry (NR), atomic force microscopy (AFM) and quartz crystal microbalance with dissipation monitoring (QCM-D), is well suited to provide quantitative information about molecular level interactions and lipid spatial distributions. In this work, cellular plasma membranes have been mimicked by designing complex SLB, containing phosphatidylinositol 4,5-bisphosphate (PtdIns4,5P) lipids as well as incorporating synthetic lipo-peptides that simulate the cytoplasmic tails of transmembrane proteins. The QCM-D results revealed that the adsorption and fusion kinetics of PtdIns4,5P are highly dependent of Mg. Additionally, it was shown that increasing concentrations of PtdIns4,5P leads to the formation of SLBs with higher homogeneity. The presence of PtdIns4,5P clusters was visualized by AFM. NR provided important insights about the structural organization of the various components within the SLB, highlighting that the leaflet symmetry of these SLBs is broken by the presence of CD4-derived cargo peptides. Finally, we foresee our study to be a starting point for more sophisticated in vitro models of biological membranes with the incorporation of inositol phospholipids and synthetic endocytic motifs.
基于固体支撑磷脂双层(SLB)的体外生物膜模型与表面敏感技术(如中子反射计(NR)、原子力显微镜(AFM)和石英晶体微天平耗散监测(QCM-D))的结合,非常适合提供关于分子水平相互作用和脂质空间分布的定量信息。在这项工作中,通过设计含有磷脂酰肌醇 4,5-二磷酸(PtdIns4,5P)脂质的复杂 SLB 并整合模拟跨膜蛋白细胞质尾巴的合成脂肽,模拟了细胞质膜。QCM-D 结果表明,PtdIns4,5P 的吸附和融合动力学高度依赖于 Mg。此外,结果表明,增加 PtdIns4,5P 的浓度会导致形成具有更高均一性的 SLB。通过 AFM 可视化了 PtdIns4,5P 簇的存在。NR 提供了关于 SLB 内各种成分结构组织的重要见解,突出表明这些 SLB 的双层对称性被 CD4 衍生货物肽的存在打破。最后,我们预计我们的研究将成为具有整合肌醇磷脂和合成内吞基序的更复杂生物膜体外模型的起点。