An in vitro protocol to assay mRNA translation inhibitors using the fluorescent assembly of the split-GFP.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2024-12-20 Epub Date: 2024-11-15 DOI:10.1016/j.xpro.2024.103448
Ana Quiroz-Huanca, Ana Sanchez-Castro, Pablo Soriano-Castillo, Chiara Poletti, Therese Manuela Nloh Tientcheu, Attilio Fabbretti, Anna Maria Giuliodori, Pohl Milon
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Abstract

Here, we present an in vitro protocol to assay mRNA translation inhibitors using the fluorescent assembly of split-GFP for translation test (FAST), based on the small fragment GFP11 binding to GFP1-10fast. We detail the expression and purification of the GFP1-10fast protein, DNA template amplification, in vitro GFP11-tagged CspA synthesis, FAST detection of the GFP11-tagged protein, and optional recovery of the fluorescent complex. In vitro synthesis of GFP11 maximizes the molar yield of synthesized proteins, providing enhanced sensitivity to test translation inhibitors. For complete details on the use and execution of this protocol, please refer to Pham et al.1.

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利用 split-GFP 的荧光组装检测 mRNA 翻译抑制剂的体外方案。
在此,我们介绍一种体外方案,利用翻译测试(FAST)的荧光组装分裂-GFP,基于小片段 GFP11 与 GFP1-10fast 的结合,检测 mRNA 翻译抑制剂。我们详细介绍了 GFP1-10fast 蛋白的表达和纯化、DNA 模板扩增、体外 GFP11 标记 CspA 合成、GFP11 标记蛋白的 FAST 检测以及可选的荧光复合物回收。体外合成 GFP11 可使合成蛋白的摩尔产量最大化,从而提高对翻译抑制剂的检测灵敏度。有关本方案使用和执行的完整细节,请参阅 Pham 等人的文章1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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