Mishra Ashish K, Mavlyutov Timur, Singh Deo R, Biener Gabriel, Yang Jay, Oliver Julie A, Ruoho Arnold, Raicu Valerică
Physics Department, University of Wisconsin-Milwaukee, Milwaukee, WI 53211, U.S.A.
Department of Neuroscience, University of Wisconsin-Madison, Madison, WI 53211, U.S.A.
Biochem J. 2015 Mar 1;466(2):263-271. doi: 10.1042/BJ20141321.
The sigma-1 receptor (S1R) is a 223-amino-acid membrane protein that resides in the endoplasmic reticulum and the plasma membrane of some mammalian cells. The S1R is regulated by various synthetic molecules including (+)-pentazocine, cocaine and haloperidol and endogenous molecules such as sphingosine, dimethyltryptamine and dehydroepiandrosterone. Ligand-regulated protein chaperone functions linked to oxidative stress and neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS) and neuropathic pain have been attributed to the S1R. Several client proteins that interact with S1R have been identified including various types of ion channels and G-protein coupled receptors (GPCRs). When S1R constructs containing C-terminal monomeric GFP2 and YFP fusions were co-expressed in COS-7 cells and subjected to FRET spectrometry analysis, monomers, dimers and higher oligomeric forms of S1R were identified under non-liganded conditions. In the presence of the prototypic S1R agonist, (+)-pentazocine, however, monomers and dimers were the prevailing forms of S1R. The prototypic antagonist, haloperidol, on the other hand, favoured higher order S1R oligomers. These data, in sum, indicate that heterologously expressed S1Rs occur in vivo in COS-7 cells in multiple oligomeric forms and that S1R ligands alter these oligomeric structures. We suggest that the S1R oligomerization states may regulate its function(s).
西格玛-1受体(S1R)是一种由223个氨基酸组成的膜蛋白,存在于某些哺乳动物细胞的内质网和质膜中。S1R受多种合成分子调节,包括(+)-喷他佐辛、可卡因和氟哌啶醇,以及内源性分子,如鞘氨醇、二甲基色胺和脱氢表雄酮。与氧化应激和神经退行性疾病(如肌萎缩侧索硬化症(ALS)和神经性疼痛)相关的配体调节蛋白伴侣功能已归因于S1R。已鉴定出几种与S1R相互作用的客户蛋白,包括各种类型的离子通道和G蛋白偶联受体(GPCR)。当含有C端单体绿色荧光蛋白2(GFP2)和黄色荧光蛋白融合体的S1R构建体在COS-7细胞中共表达并进行荧光共振能量转移(FRET)光谱分析时,在非配体条件下鉴定出S1R的单体、二聚体和更高的寡聚体形式。然而,在原型S1R激动剂(+)-喷他佐辛存在的情况下,单体和二聚体是S1R的主要形式。另一方面,原型拮抗剂氟哌啶醇则有利于形成更高阶的S1R寡聚体。总之,这些数据表明,在COS-7细胞中异源表达的S1R在体内以多种寡聚体形式存在,并且S1R配体可改变这些寡聚体结构。我们认为S1R的寡聚化状态可能调节其功能。