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完整的尿激酶受体是有效结合玻连蛋白所必需的:受体裂解会阻止配体相互作用。

The intact urokinase receptor is required for efficient vitronectin binding: receptor cleavage prevents ligand interaction.

作者信息

Høyer-Hansen G, Behrendt N, Ploug M, Danø K, Preissner K T

机构信息

Finsen Laboratory, Rigshospitalet, Copenhagen O, Denmark.

出版信息

FEBS Lett. 1997 Dec 22;420(1):79-85. doi: 10.1016/s0014-5793(97)01491-9.

Abstract

The urokinase receptor (uPAR) is a receptor for both urokinase plasminogen activator (uPA) and the adhesion protein vitronectin. There are two forms of cell surface-bound uPAR; intact uPAR and a cleaved form, uPAR(2+3), which is formed by uPA-catalyzed cleavage of uPAR. In ligand-blotting experiments we found that vitronectin binds uPAR but not uPAR(2+3). In real-time biomolecular interaction analysis using recombinant, soluble uPAR (suPAR) both plasma and multimeric forms of vitronectin bound to intact, antibody-immobilized suPAR. Monoclonal antibodies against domain 1 of uPAR blocked suPAR binding to vitronectin and vitronectin did not interact with suPAR(2+3). Both suPAR(2+3) and the isolated domain 1 failed to compete with the intact suPAR in binding to vitronectin. We therefore conclude that the intact receptor is required for efficient vitronectin binding.

摘要

尿激酶受体(uPAR)是尿激酶型纤溶酶原激活剂(uPA)和黏附蛋白玻连蛋白的受体。细胞表面结合的uPAR有两种形式:完整的uPAR和一种裂解形式uPAR(2 + 3),后者由uPA催化裂解uPAR形成。在配体印迹实验中,我们发现玻连蛋白结合uPAR,但不结合uPAR(2 + 3)。在使用重组可溶性uPAR(suPAR)的实时生物分子相互作用分析中,血浆形式和多聚体形式的玻连蛋白均与完整的、抗体固定的suPAR结合。针对uPAR结构域1的单克隆抗体阻断了suPAR与玻连蛋白的结合,且玻连蛋白不与uPAR(2 + 3)相互作用。suPAR(2 + 3)和分离出的结构域1在与玻连蛋白结合时均无法与完整的suPAR竞争。因此,我们得出结论,有效的玻连蛋白结合需要完整的受体。

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