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A selective calix6arene-based fluorescent chemosensor for phosphatidylcholine type lipids

机译:一种选择性碱6基于氨基荧光化学传感器,用于磷脂酰胆碱型脂质

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摘要

The development of chemosensors that can selectively detect phosphatidylcholines (PCs) in biological samples is of medical relevance considering the importance of these phospholipids in cell growth and survival. Their selective sensing over phosphatidylethanolamines (PEs) is however a challenging task. We report here on the chemosensing capacities of calix[6]tris-pyrenylurea 1, which is able to selectively interact with phosphatidylcholine-type lipids in organic media. Host 1 also binds them in a biphasic chloroform/water solution, opening the way to the design of selective chemosensors for these lipids in biological media. The results obtained by NMR, fluorescence spectroscopy and modelling studies show that the selectivity is the result of the high degree of complementarity between the lipids' zwitterionic phosphatidylcholine headgroup and the receptor's H-bonding donor site and hydrophobic pocket. The mode of recognition is reminiscent of natural systems, such as human phosphatidylcholine transfer proteins (PC-TPs), validating the biomimetic approach adopted in our work.
机译:考虑到这些磷脂在细胞生长和存活中的重要性,可以选择性地检测生物样品中的化学传感器的开发具有医学相关性。然而,它们对磷脂酰乙醇胺(PE)的选择性感测是一个具有挑战性的任务。我们在此报告CALIX [6] TRIS-PYRENYLUREA 1的化学溶解能力,其能够在有机培养基中选择性地与磷脂酰胆碱型脂质相互作用。宿主1还将它们粘合在双相氯仿/水溶液中,在生物介质中为这些脂质的选择性化学传感器设计开辟了途径。通过NMR,荧光光谱学和建模研究获得的结果表明,选择性是脂质的两性离子磷脂酰胆碱标题和受体的H键合供体部位和疏水口袋之间的高互补程度的结果。识别方式使耐受天然系统,例如人磷脂酰胆碱转移蛋白(PC-TPS),验证我们工作中采用的仿生方法。

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