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Bile acid binding protein: a versatile host of small hydrophobic ligands for applications in the fields of MRI contrast agents and bio-nanomaterials

机译:胆汁酸结合蛋白:多种小型疏水性配体可用于MRI造影剂和生物纳米材料领域

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摘要

During the last decade a growing amount of evidence has been obtained, supporting the role of the beta-clamshell family of intracellular lipid binding proteins (iLBPs) not only in the translocation of lipophilic molecules but also in lipid mediated signalling and metabolism. Given the central role of lipids in physiological processes, it is essential to have detailed knowledge on their interactions with cognate binding proteins. Structural and dynamical aspects of the binding mechanisms have been widely investigated by means of NMR spectroscopy, docking and molecular dynamics simulation approaches. iLBPs share a stable beta-barrel fold, delimiting an internal cavity capable of promiscuous ligand binding and display significant flexibility at the putative ligand portal. These features make this class of proteins good scaffolds to build host-guest systems for applications in nanomedicine and nanomaterials.
机译:在过去的十年中,已经获得了越来越多的证据,这些证据不仅支持β蛤壳细胞内脂质结合蛋白(iLBP)家族在亲脂性分子的转运中,而且在脂质介导的信号传导和代谢中的作用。考虑到脂质在生理过程中的核心作用,对它们与同源结合蛋白的相互作用的详细了解至关重要。结合机制的结构和动力学方面已通过NMR光谱,对接和分子动力学模拟方法进行了广泛研究。 iLBPs共享一个稳定的β-桶形折叠,界定了一个能够混配配体的内部空腔,并在推定的配体门户处显示出显着的柔韧性。这些特性使这类蛋白质成为构建用于纳米药物和纳米材料的宿主系统的良好支架。

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