Institute for Pharmaceutical Sciences, University of Freiburg , Hermann-Herder-Straße 9, Freiburg im Breisgau 79104, Germany.
BIOSS Centre for Biological Signalling Studies, University of Freiburg , Schänzlestraße 18, Freiburg im Breisgau 79104, Germany.
Langmuir. 2018 Feb 6;34(5):1999-2005. doi: 10.1021/acs.langmuir.7b03189. Epub 2018 Jan 29.
The asymmetric distribution of lipids between the two bilayer leaflets represents a typical feature of biological membranes. The loss of this asymmetry, for example the exposure of negatively charged lipids on the extracellular membrane leaflet of mammalian cells, is involved in apoptosis and occurs in tumor cells. Thus, the controlled production of asymmetric liposomes helps to better understand such crucial cellular processes. Here, we present an approach that allows us to design asymmetric model-membrane experiments on a rational basis and predict the fraction of exchanged lipid. In addition, we developed a label-free and nondestructive assay to quantify the asymmetric uptake of negatively charged lipids in terms of the zeta potential. This significantly enhances the applicability, impact, and predictive power of model membranes.
脂质在双层膜叶之间的不对称分布是生物膜的典型特征。这种不对称性的丧失,例如哺乳动物细胞膜外叶层带负电荷的脂质暴露,与细胞凋亡有关,并发生在肿瘤细胞中。因此,控制不对称脂质体的产生有助于更好地理解这些关键的细胞过程。在这里,我们提出了一种方法,使我们能够在合理的基础上设计不对称模型膜实验,并预测交换脂质的分数。此外,我们开发了一种无标记和非破坏性的测定法,以 ζ 电位的形式定量测量带负电荷的脂质的不对称摄取。这显著提高了模型膜的适用性、影响力和预测能力。