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邻苯二甲酸酯和苯氧羧酸类除草剂环境污染物与肠道细胞内脂质结合蛋白的相互作用。

Interaction of phthalates and phenoxy acid herbicide environmental pollutants with intestinal intracellular lipid binding proteins.

机构信息

Animal Nutrition and Health, AgResearch Limited, Grasslands Research Centre, Tennent Drive, Private Bag 11008, Palmerston North 4442, New Zealand.

出版信息

Chem Res Toxicol. 2013 Aug 19;26(8):1240-50. doi: 10.1021/tx400170t. Epub 2013 Jul 24.

Abstract

Transcellular diffusion across the columnar absorptive epithelial cells (enterocytes) of the small intestine is a major route of absorption for phthalate and phenoxy acid herbicide environmental pollutants that have been associated with adverse human health effects. The biochemical mechanisms responsible for the transport of these pollutants across the enterocyte, however, remain poorly characterized. In the present study, we have shown that the innate intestinal intracellular lipid binding proteins (iLBPs), namely, intestinal (I) and liver (L)-fatty acid binding proteins (FABP) bind to phthalate and phenoxy acid herbicides. The relative affinities of the compounds were determined by fluorescence competition assays, and a 3D-QSAR model was established for L-FABP. Structural information obtained from NMR chemical shift perturbation and molecular docking experiments defined the binding sites. Differential scanning calorimetry and proteolysis experiments revealed that the binding of these compounds produces stabilizing conformational changes in the structure of I-FABP. In summary, the presented biophysical data suggests that the binding of phthalate and phenoxy acid herbicides to intestinal iLBPs may increase the cytosolic solubility of these compounds and thereby may facilitate their transport from the intestinal lumen across the enterocyte to sites of distribution and metabolism.

摘要

肠腔柱状吸收上皮细胞(肠上皮细胞)的细胞旁扩散是邻苯二甲酸酯和苯氧羧酸类除草剂等环境污染物吸收的主要途径,这些污染物与人类健康的不良影响有关。然而,负责这些污染物穿过肠上皮细胞运输的生化机制仍知之甚少。在本研究中,我们已经表明,固有肠内细胞内脂质结合蛋白(iLBPs),即肠(I)和肝(L)脂肪酸结合蛋白(FABP)与邻苯二甲酸酯和苯氧羧酸类除草剂结合。通过荧光竞争测定法确定了化合物的相对亲和力,并为 L-FABP 建立了 3D-QSAR 模型。从 NMR 化学位移扰动和分子对接实验获得的结构信息定义了结合位点。差示扫描量热法和蛋白水解实验表明,这些化合物的结合会导致 I-FABP 结构发生稳定的构象变化。总之,所提出的生物物理数据表明,邻苯二甲酸酯和苯氧羧酸类除草剂与肠内 iLBPs 的结合可能会增加这些化合物在细胞溶质中的溶解度,从而有助于它们从肠腔穿过肠上皮细胞运输到分布和代谢部位。

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