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Real-Time In-Cell Nuclear Magnetic Resonance: Ribosome-Targeted Antibiotics Modulate Quinary Protein Interactions

机译:实时内细胞核磁共振:核糖体靶向抗生素调节静脉蛋白相互作用

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摘要

How ribosome antibiotics affect a wide range of biochemical pathways is not well understood; changes in RNA-mediated protein quinary interactions and consequent activity inside the crowded cytosol may provide one possible mechanism. We developed real-time (RT) in-cell nuclear magnetic resonance (NMR) spectroscopy to monitor temporal changes in protein quinary structure, for = 24 h, in response to external and internal stimuli. RT in-cell NMR consists of a bioreactor containing gel-encapsulated cells inside a 5 mm NMR tube, a gravity siphon for continuous exchange of medium, and a horizontal drip irrigation system to supply nutrients to the cells during the experiment. We showed that adding antibiotics that bind to the small ribosomal subunit results in more extensive quinary interactions between thioredoxin and mRNA. The results substantiate the idea that RNA-mediated modulation of quinary protein interactions may provide the physical basis for ribosome inhibition and other regulatory pathways.
机译:核糖体抗生素如何影响广泛的生化途径并不充分理解; RNA介导的蛋白质乳腺相互作用的变化和拥挤的细胞溶胶内部的随后活动可以提供一种可能的机制。我们开发了实时(RT)内细胞核磁共振(NMR)光谱,以监测蛋白质谐析结构的时间变化,响应外部和内部刺激,= 24小时。室温NMR由含有含有凝胶包封的细胞的生物反应器,在5mm NMR管内,用于连续交换培养基的重力虹吸管,以及在实验期间向细胞供应营养物质。我们表明,添加与小核糖体亚基的抗生素导致硫昔林和mRNA之间更广泛的奇异相互作用。结果证实了RNA介导的乳腺蛋白相互作用调节的想法可以为核糖体抑制和其他调节途径提供物理基础。

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