Department of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA 52242; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, AK 72205; and.
Department of Pharmacology, University of Iowa Carver College of Medicine, Iowa City, IA 52242.
J Lipid Res. 2012 Oct;53(10):2214-2225. doi: 10.1194/jlr.D026468. Epub 2012 Jul 20.
The submicroscopic spatial organization of cell surface receptors and plasma membrane signaling molecules is readily characterized by electron microscopy (EM) via immunogold labeling of plasma membrane sheets. Although various signaling molecules have been seen to segregate within plasma membrane microdomains, the biochemical identity of these microdomains and the factors affecting their formation are largely unknown. Lipid rafts are envisioned as submicron membrane subdomains of liquid ordered structure with differing lipid and protein constituents that define their specific varieties. To facilitate EM investigation of inner leaflet lipid rafts and the localization of membrane proteins therein, a unique genetically encoded reporter with the dually acylated raft-targeting motif of the Lck kinase was developed. This reporter, designated Lck-BAP-GFP, incorporates green fluorescent protein (GFP) and biotin acceptor peptide (BAP) modules, with the latter allowing its single-step labeling with streptavidin-gold. Lck-BAP-GFP was metabolically biotinylated in mammalian cells, distributed into low-density detergent-resistant membrane fractions, and was readily detected with avidin-based reagents. In EM images of plasma membrane sheets, the streptavidin-gold-labeled reporter was clustered in 20-50 nm microdomains, presumably representative of inner leaflet lipid rafts. The utility of the reporter was demonstrated in an investigation of the potential lipid raft localization of the epidermal growth factor receptor.
细胞表面受体和质膜信号分子的亚微观空间组织可以通过电子显微镜(EM)通过质膜薄片的免疫金标记来轻松表征。尽管已经看到各种信号分子在质膜微区中分隔开,但这些微区的生化身份以及影响它们形成的因素在很大程度上是未知的。脂筏被设想为具有不同脂质和蛋白质成分的亚微米膜亚区,这些成分定义了它们的特定种类。为了促进对质膜内层脂筏的 EM 研究以及其中膜蛋白的定位,开发了一种具有 Lck 激酶的双酰化筏靶向基序的独特遗传编码报告蛋白。该报告蛋白命名为 Lck-BAP-GFP,包含绿色荧光蛋白(GFP)和生物素接受肽(BAP)模块,后者允许其与链霉亲和素-金进行单步标记。Lck-BAP-GFP 在哺乳动物细胞中被代谢生物素化,分布在低密度去污剂抗性膜部分中,并可通过基于亲和素的试剂轻松检测到。在质膜薄片的 EM 图像中,链霉亲和素-金标记的报告蛋白聚集在 20-50nm 的微区中,推测代表质膜内层脂筏。该报告蛋白的用途在表皮生长因子受体的潜在脂筏定位研究中得到了证明。