通过实时监测无细胞翻译筛选适合将非天然氨基酸引入蛋白质的琥珀色抑制trna。

Issei Iijima, Takahiro Hohsaka
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引用次数: 0

摘要

将非天然氨基酸掺入蛋白质中是分析蛋白质结构和功能的一种有用技术。我们已经报道了琥珀色抑制trna,通过筛选大肠杆菌中多种天然存在的trna,可以获得适合于有效和特异性地将非天然氨基酸整合到蛋白质中。无细胞翻译系统。通过结合荧光非天然氨基酸和无细胞翻译产物的荧光SDS-PAGE分析来评估trna的琥珀色抑制活性,尽管SDS-PAGE分析既麻烦又耗时。在这项研究中,我们开发了一种筛选琥珀色抑制trna的替代方法,通过实时测量从GFP到bodipy558连接的非天然氨基酸的荧光共振能量转移(FRET),琥珀色抑制trna被纳入GFP的n端。利用这种方法,我们证明了各种原核Trp trna的琥珀色抑制活性的筛选是高通量的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening of amber suppressor tRNAs suitable to introduce nonnatural amino acids into proteins by real-time monitoring of cell-free translation.

Incorporation of nonnatural amino acids into proteins is a useful technique to analyze protein structure and function. We have reported that amber suppressor tRNAs suitable for efficient and specific incorporation of nonnatural amino acids into proteins can be obtained by screening a wide variety of naturally occurring tRNAs in an E. coli. cell-free translation system. The amber suppressor activity of the tRNAs was evaluated by incorporation of a fluorescent nonnatural amino acid and fluorescent SDS-PAGE analysis of cell-free translation products, though the SDS-PAGE was troublesome and time-consuming. In this research, we developed an alternative method for the screening of amber suppressor tRNAs by real-time measurement of fluorescence resonance energy transfer (FRET) from GFP to BODIPY558-linked nonnatural amino acid, which was incorporated into the N-terminus of GFP by amber suppressor tRNAs. Using this method, we demonstrated that the screening of the amber suppressor activity of various prokaryotic Trp tRNAs was performed in a high-throughput manner.

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