Irwin Michael J, Wang Xin, Cote Rick H
Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA.
Bio Protoc. 2022 Jan 20;12(2):e4303. doi: 10.21769/BioProtoc.4303.
G-protein coupled signaling pathways are organized into multi-protein complexes called signalosomes that are located within and on cellular membranes. We describe the use of silica nanoparticles coated with a unilamellar phospholipid bilayer (lipobeads) to reconstitute the activated photoreceptor G-protein α-subunit (Gtα*) with its cognate effector (phosphodiesterase-6; PDE6) for biochemical and structural studies of the activation mechanism regulating this GPCR signaling pathway. Lipobeads are prepared by resuspending dried-down phospholipid mixtures with monodisperse 70 nm silica particles, followed by extrusion through a 100 nm membrane filter. This uniform and supported liposomal preparation is easily sedimented, permitting the separation of soluble from membrane-associated proteins. Upon loading lipobeads with Gtα* and PDE6, we find that activation of PDE6 catalysis by Gtα* occurs much more efficiently than in the absence of membranes. Chemical cross-linking of membrane-confined proteins allows detection of changes in protein-protein interactions, resulting from G-protein activation of PDE6. The advantages of using lipobeads over partially purified membrane preparations or traditional liposomal preparations are generally applicable to the study of other membrane-confined signal transduction pathways.
G蛋白偶联信号通路被组织成称为信号小体的多蛋白复合物,这些复合物位于细胞膜内和细胞膜上。我们描述了使用包被有单层磷脂双分子层的二氧化硅纳米颗粒(脂质珠)来将活化的光感受器G蛋白α亚基(Gtα*)与其同源效应器(磷酸二酯酶-6;PDE6)进行重组,以用于对调节该GPCR信号通路的激活机制进行生化和结构研究。脂质珠是通过将干燥的磷脂混合物与单分散的70纳米二氧化硅颗粒重悬,然后通过100纳米的膜过滤器挤出而制备的。这种均匀且有支撑的脂质体制剂很容易沉淀,从而可以将可溶性蛋白与膜相关蛋白分离。在用Gtα和PDE6加载脂质珠后,我们发现Gtα对PDE6催化的激活比在没有膜的情况下效率要高得多。对膜限制蛋白进行化学交联可以检测由于PDE6的G蛋白激活而导致的蛋白-蛋白相互作用的变化。与部分纯化的膜制剂或传统脂质体制剂相比,使用脂质珠的优势通常适用于其他膜限制信号转导通路的研究。