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通过含硫代磷酸酯的tRNA转录本足迹法测定大肠杆菌tRNA(Ser)与其同源氨酰-tRNA合成酶的相互作用。

Interaction of Escherichia coli tRNA(Ser) with its cognate aminoacyl-tRNA synthetase as determined by footprinting with phosphorothioate-containing tRNA transcripts.

作者信息

Schatz D, Leberman R, Eckstein F

机构信息

Max-Planck-Institut für experimentelle Medizin, Abteilung Chemie, Göttingen, Federal Republic of Germany.

出版信息

Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6132-6. doi: 10.1073/pnas.88.14.6132.

Abstract

A footprinting technique using phosphorothioate-containing RNA transcripts has been developed and applied to identify contacts between Escherichia coli tRNA(Ser) and its cognate aminoacyl-tRNA synthetase. The cloned gene for the tRNA was transcribed in four reactions in which a different NTP was complemented by 5% of the corresponding nucleoside 5'-O-(1-thiotriphosphate). The phosphorothioate groups of such transcripts are cleaved by reaction with iodine to permit sequencing of the transcripts. Footprinting was achieved by performing the same reaction with the phosphorothioate-tRNA-enzyme complex. At 1 mM iodine, selective protection of the tRNA transcripts in the cognate system was observed, with strong protection at positions 52 and 68 and weak protection at positions 46, 53, 67, 69, and 70. It is suggested that these regions of the tRNA interact with the helical arm of the synthetase.

摘要

一种使用含硫代磷酸酯的RNA转录本的足迹技术已被开发出来,并应用于鉴定大肠杆菌tRNA(Ser)与其同源氨酰tRNA合成酶之间的相互作用。tRNA的克隆基因在四个反应中进行转录,其中不同的NTP由5%相应的核苷5'-O-(1-硫代三磷酸)补充。这些转录本的硫代磷酸酯基团通过与碘反应而被切割,从而允许对转录本进行测序。通过对硫代磷酸酯-tRNA-酶复合物进行相同反应来实现足迹分析。在1 mM碘的条件下,在同源系统中观察到tRNA转录本的选择性保护,在位置52和68处有强烈保护,在位置46、53、67、69和70处有较弱保护。有人认为,tRNA的这些区域与合成酶的螺旋臂相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/297c/52036/84c02f86c85e/pnas01064-0205-a.jpg

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