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Nonorthogonal tRNA(Amber)(cys) for protein and nascent chain labeling

机译:非正交tRNA(琥珀)(cys)用于蛋白质和新生链标记

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In vitro-transcribed suppressor tRNAs are commonly used in site-specific fluorescence labeling for protein and ribosome-bound nascent chains (RNCs) studies. Here, we describe the production of nonorthogonal Bacillus subtilis tRNA(Amber)(cys) from Escherichia coli, a process that is superior to in vitro transcription in terms of yield, ease of manipulation, and tRNA stability. As cysteinyl-tRNA synthetase was previously shown to aminoacylate tRNA(Amber)(cys) with lower efficiency, multiple tRNA synthetase mutants were designed to optimize aminoacylation. Aminoacylated tRNA was conjugated to a fluorophore to produce BODIPY FL-cysteinyl-tRNA(Amber)(cys), which was used to generate ribosome-bound nascent chains of different lengths with the fluorophore incorporated at various predetermined sites. This tRNA tool may be beneficial in the site-specific labeling of full-length proteins as well as RNCs for biophysical and biological research.
机译:体外转录的抑制性tRNA通常用于蛋白质和核糖体结合的新生链(RNC)研究的位点特异性荧光标记。在这里,我们描述了从大肠杆菌中产生的非正交枯草芽孢杆菌tRNA(Amber)(cys),在产量,易于操作和tRNA稳定性方面优于体外转录的过程。由于半胱氨酸-tRNA合成酶以前显示出较低效率的氨基酰化tRNA(Amber)(cys),因此设计了多个tRNA合成酶突变体来优化氨基酰化。将氨基酰化的tRNA与荧光团缀合以产生BODIPY FL-半胱氨酰-tRNA(Amber)(cys),将其用于生成具有不同长度的核糖体结合的新生链,并在各个预定位点掺入荧光团。该tRNA工具可能在全长蛋白以及用于生物物理和生物学研究的RNC的位点特异性标记中是有益的。

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