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Design Synthesis and Biological Activity of Novel Triazole Amino Acids Used To Probe Binding Interactions Between Ligand and Neutral Amino Acid Transport Protein SN1

机译:用于探测配体和中性氨基酸转运蛋白SN1之间的结合相互作用的新型三唑氨基酸的设计合成和生物活性

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摘要

Novel triazole amino acids were synthesized as probes to investigate ligand-protein binding interactions of the neutral amino acid transporter SN1. The bonding hypothesis to be tested was that the side chains of endogenous substrates are acting as H-bond acceptors. Although limited inhibition of 3H-L-glutamine uptake by SN1 expressing oocytes was observed, the synthetic compounds show a trend that suggests a hydrogen bond interaction just outside the endogenous ligand binding pocket.
机译:合成了新型三唑氨基酸作为探针,以研究中性氨基酸转运蛋白SN1的配体-蛋白质结合相互作用。要测试的键合假设是内源性底物的侧链充当氢键受体。尽管观察到对表达SN1的卵母细胞对 3 H-L-谷氨酰胺摄取的抑制作用有限,但合成的化合物显示出一种趋势,表明在内源性配体结合口袋外部有氢键相互作用。

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