Calvete J J, Henschen A, González-Rodríguez J
Instituto de Química Física, C.S.I.C., Madrid, Spain.
Biochem J. 1991 Feb 15;274 ( Pt 1)(Pt 1):63-71. doi: 10.1042/bj2740063.
Integrins are cell-surface heterodimers formed by the association of one alpha- and one beta-subunit. Glycoprotein IIIa (GPIIIa or beta 3 subunit) is the common beta-subunit of the beta 3 subfamily of integrins, which, when associated with glycoprotein IIb (GPIIb), constitutes the receptor for fibrinogen and other adhesive proteins at the platelet surface (the GPIIb-IIIa complex) and, when associated with the alpha v-subunit, constitutes the vitronectin receptor present in several cell types. Protein chemical analysis of GPIIIa allows us to define the following structural domains: the cysteine-rich and proteinase-resistant N-terminal domain (GPIIIa 1-62); the adhesive-protein-binding domain (GPIIIa 101-422); the cysteine-rich and proteinase-resistant core (GPIIIa 423-622); and the C-terminal domain comprising an extracellular subdomain (GPIIIa 623-692), a transmembrane subdomain (GPIIIa 693-721), and a cytoplasmic subdomain (GPIIIa 722-762). We also assign unambiguously the disulphide bonds within the N-terminal, the fibrinogen-binding and the C-terminal domains, and the two long-range disulphide bonds which join the N-terminus to the proteinase-resistant core (Cys5-Cys435) and the fibrinogen-binding domain to the extracellular side of the C-terminal domain (Cys406-Cys655). In addition, we propose three alternative models for the arrangement of the disulphide bonds within the core and of the disulphide bonds joining the core to the extracellular side of the C-terminal domain, consistent with our experimental findings, favouring temporarily that which imposes less steric hindrance for the formation of these disulphide bonds. On the basis of this information and on the highly conserved overall structure observed in the beta-subunits of the integrin family known so far, except in beta 4, we propose to extend the cysteine-pairing pattern and the structural domains outlined here for GPIIIa to all the beta-subunits of the integrin family.
整合素是由一个α亚基和一个β亚基结合形成的细胞表面异二聚体。糖蛋白IIIa(GPIIIa或β3亚基)是整合素β3亚家族的常见β亚基,当与糖蛋白IIb(GPIIb)结合时,构成血小板表面纤维蛋白原和其他黏附蛋白的受体(GPIIb-IIIa复合物),当与αv亚基结合时,构成存在于多种细胞类型中的玻连蛋白受体。对GPIIIa进行蛋白质化学分析使我们能够确定以下结构域:富含半胱氨酸且抗蛋白酶的N端结构域(GPIIIa 1-62);黏附蛋白结合结构域(GPIIIa 101-422);富含半胱氨酸且抗蛋白酶的核心结构域(GPIIIa 423-622);以及包含细胞外亚结构域(GPIIIa 623-692)、跨膜亚结构域(GPIIIa 693-721)和细胞质亚结构域(GPIIIa 722-762)的C端结构域。我们还明确确定了N端、纤维蛋白原结合结构域和C端结构域内的二硫键,以及将N端与抗蛋白酶核心连接起来的两个长程二硫键(Cys5-Cys435)和将纤维蛋白原结合结构域与C端结构域细胞外侧连接起来的二硫键(Cys406-Cys655)。此外,我们提出了三种关于核心结构域内二硫键以及将核心结构域与C端结构域细胞外侧连接起来的二硫键排列的替代模型,这些模型与我们的实验结果一致,暂时倾向于对这些二硫键形成空间位阻较小的模型。基于这些信息以及到目前为止在整合素家族β亚基中观察到的高度保守的整体结构(除β4外),我们建议将此处为GPIIIa概述的半胱氨酸配对模式和结构域扩展到整合素家族的所有β亚基。