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Roles of the structure and orientation of ligands and ligand mimics inside the ligand-binding pocket of the vitamin D-binding protein

机译:维生素D结合蛋白的配体结合口袋内配体的结构和取向以及配体模拟物的作用

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摘要

1alpha,25-Dihydroxyvitamin D3, the vitamin D hormone, manifests its diverse biological properties by specifically binding to the vitamin D sterol-binding pockets of vitamin D-binding protein (DBP) and vitamin D receptor. In the past, several affinity, photoaffinity, and chemical modification studies have been carried out to probe the vitamin D sterol-binding pocket of DBP and to evaluate the relationship between the structure of this pocket and the functions of the protein. In the present study, we examined the steric requirements inside this pocket by considering conformational structures of various bromoacetate derivatives of 25-hydroxyvitamin D3 and 1alpha,25-dihydroxyvitamin D3 and their abilities to covalently and specifically modify this pocket. We observed that, although 25-hydroxyvitamin D3 3beta-bromoacetate (25-OH-D3-3-BE), 1alpha,25-dihydroxyvitamin D3 3beta-bromoacetate [1alpha,25(OH)2D3-3-BE], 1alpha,25-dihydroxyvitamin D3 1alpha-bromoacetate [1alpha,25(OH)2D3-1-BE], and 1alpha,25-dihydroxyvitamin D3 1alpha,3beta-dibromoacetate [1alpha,25(OH)2D3-1,3-di-BE] bound DBP in a specific manner, only [3H]-25-OH-D3-3-BE and [3H]-1alpha,25(OH)2D3-3-BE affinity labeled the protein. BNPS-skatole cleavages of [3H]-25-OH-D3-3-BE- and 3H-1alpha,25(OH)2D3-3-BE-labeled DBP samples produced the same labeled peptide (N-terminal), demonstrating the specificity of labeling by these analogs. Energy-minimized conformational structures of these bromoacetate derivatives indicated significant changes in the A-ring conformations of these analogs. These structural changes were invoked to explain the inability of [3H]-1alpha,25(OH)2D3-1-BE and [3H]-1alpha,25(OH)2D3-1,3-di-BE to affinity label DBP. Overall, these studies suggested that the vitamin D sterol-binding pocket in DBP is sterically quite restrictive. This information could be potentially important in designing future vitamin D-based drugs for several diseases.
机译:维生素D激素1alpha,25-Dihydroxyvitamin D3通过与维生素D结合蛋白(DBP)和维生素D受体的维生素D固醇结合口袋特异性结合,表现出其多种生物学特性。过去,已进行了几项亲和力,光亲和力和化学修饰研究,以探测DBP的维生素D固醇结合口袋,并评估该口袋的结构与蛋白质功能之间的关系。在本研究中,我们通过考虑25-羟基维生素D3和1α,25-二羟基维生素D3的各种溴乙酸盐衍生物的构象结构及其共价和特异性修饰该口袋的能力,研究了该口袋内的空间需求。我们观察到,尽管25-羟基维生素D33β-溴乙酸盐(25-OH-D3-3-BE),1alpha,25-二羟基维生素D33β-溴乙酸盐[1alpha,25(OH)2D3-3-BE],1alpha,25 -dihydroxyvitamin D3 1alpha-bromoacetate [1alpha,25(OH)2D3-1-BE]和1alpha,25-dihydroxyvitamin D3 1alpha,3beta-dibromoacetate [1alpha,25(OH)2D3-1,3-di-BE]结合DBP以特定的方式,只有[3H] -25-OH-D3-3-BE和[3H] -1alpha,25(OH)2D3-3-BE亲和性标记了该蛋白质。 [3H] -25-OH-D3-3-BE-和3H-1alpha,25(OH)2D3-3-BE标记的DBP样品的BNPS粪便裂解产生相同的标记肽(N端),表明这些类似物标记的特异性。这些溴乙酸衍生物的能量最小的构象结构表明这些类似物的A环构象发生了显着变化。调用这些结构变化来解释[3H] -1alpha,25(OH)2D3-1-BE和[3H] -1alpha,25(OH)2D3-1,3-di-BE对亲和标记DBP的无效性。总体而言,这些研究表明DBP中的维生素D固醇结合口袋在空间上具有限制性。该信息对于设计针对多种疾病的未来基于维生素D的药物可能具有潜在的重要性。

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