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Protein- protein interaction detection system using fluorescent protein microdomains

机译:使用荧光蛋白微区的蛋白-蛋白相互作用检测系统

摘要

The invention provides a protein labeling and interaction detection system based on engineered fragments of fluorescent and chromophoric proteins that require fused interacting polypeptides to drive the association of the fragments, and further are soluble and stable, and do not change the solubility of polypeptides to which they are fused. In one embodiment, a test protein X is fused to a sixteen amino acid fragment of GFP (β-strand 10, amino acids 198-214), engineered to not perturb fusion protein solubility. A second test protein Y is fused to a sixteen amino acid fragment of GFP (β-strand 11, amino acids 215-230), engineered to not perturb fusion protein solubility. When X and Y interact, they bring the GFP strands into proximity, and are detected by complementation with a third GFP fragment consisting of GFP amino acids 1-198 (strands 1-9). When GFP strands 10 and 11 are held together by interaction of protein X and Y, they spontaneous association with GFP strands 1-9, resulting in structural complementation, folding, and concomitant GFP fluorescence.
机译:本发明提供了基于荧光和发色蛋白质的工程片段的蛋白质标记和相互作用检测系统,所述荧光和发色蛋白质的工程片段需要融合的相互作用多肽来驱动片段的缔合,并且进一步是可溶的和稳定的,并且不改变它们所针对的多肽的溶解度被融合。在一个实施方案中,将测试蛋白X融合至GFP的16个氨基酸片段(β-链10,氨基酸198-214),其经工程改造以不干扰融合蛋白的溶解性。将第二种测试蛋白Y融合到GFP的16个氨基酸片段(β链11,第215-230位氨基酸)上,以不干扰融合蛋白的溶解度。当X和Y相互作用时,它们使GFP链接近,并通过与由GFP氨基酸1-198(链1-9)组成的第三个GFP片段互补而被检测到。当GFP链10和11通过蛋白质X和Y的相互作用结合在一起时,它们与GFP链1-9自发结合,导致结构互补,折叠和伴随的GFP荧光。

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