Feng Yiqing, Kochovski Zdravko, Arenz Christoph, Lu Yan, Kneipp Janina
Department of Chemistry, Humboldt-Universität zu Berlin, Brook-Taylor-Straße 2, 12489 Berlin, Germany.
Einstein Center of Catalysis (EC2/BIG-NSE), Technische Universität Berlin, Marchstraße 6-8, 10587 Berlin, Germany.
J Phys Chem C Nanomater Interfaces. 2022 Aug 11;126(31):13237-13246. doi: 10.1021/acs.jpcc.2c01930. Epub 2022 Jul 27.
Due to the great potential of surface-enhanced Raman scattering (SERS) as local vibrational probe of lipid-nanostructure interaction in lipid bilayers, it is important to characterize these interactions in detail. The interpretation of SERS data of lipids in living cells requires an understanding of how the molecules interact with gold nanostructures and how intermolecular interactions influence the proximity and contact between lipids and nanoparticles. Ceramide, a sphingolipid that acts as important structural component and regulator of biological function, therefore of interest to probing, lacks a phosphocholine head group that is common to many lipids used in liposome models. SERS spectra of liposomes of a mixture of ceramide, phosphatidic acid, and phosphatidylcholine, as well as of pure ceramide and of the phospholipid mixture are reported. Distinct groups of SERS spectra represent varied contributions of the choline, sphingosine, and phosphate head groups and the structures of the acyl chains. Spectral bands related to the state of order of the membrane and moreover to the amide function of the sphingosine head groups indicate that the gold nanoparticles interact with molecules involved in different intermolecular relations. While cryogenic electron microscopy shows the formation of bilayer liposomes in all preparations, pure ceramide was found to also form supramolecular, concentric stacked and densely packed lamellar, nonliposomal structures. That the formation of such supramolecular assemblies supports the intermolecular interactions of ceramide is indicated by the SERS data. The unique spectral features that are assigned to the ceramide-containing lipid model systems here enable an identification of these molecules in biological systems and allow us to obtain information on their structure and interaction by SERS.
由于表面增强拉曼散射(SERS)作为脂质双层中脂质-纳米结构相互作用的局部振动探针具有巨大潜力,详细表征这些相互作用非常重要。对活细胞中脂质的SERS数据进行解释需要了解分子如何与金纳米结构相互作用,以及分子间相互作用如何影响脂质与纳米颗粒之间的接近程度和接触。神经酰胺是一种鞘脂,作为重要的结构成分和生物功能调节剂,因此是研究的对象,它缺乏许多用于脂质体模型的脂质所共有的磷酸胆碱头部基团。本文报道了神经酰胺、磷脂酸和磷脂酰胆碱混合物的脂质体以及纯神经酰胺和磷脂混合物的SERS光谱。不同组的SERS光谱代表了胆碱、鞘氨醇和磷酸头部基团以及酰基链结构的不同贡献。与膜的有序状态以及鞘氨醇头部基团的酰胺功能相关的光谱带表明金纳米颗粒与参与不同分子间关系的分子相互作用。虽然低温电子显微镜显示所有制剂中都形成了双层脂质体,但发现纯神经酰胺还形成了超分子、同心堆叠且紧密堆积的层状非脂质体结构。SERS数据表明这种超分子组装的形成支持了神经酰胺的分子间相互作用。此处分配给含神经酰胺脂质模型系统的独特光谱特征能够在生物系统中识别这些分子,并使我们能够通过SERS获得有关它们的结构和相互作用的信息。