Nishikawa Yuma, Fujikawa Riko, Nakano Hideo, Kanamori Takashi, Ojima-Kato Teruyo
Laboratory of Molecular Biotechnology, Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
GeneFrontier Corporation, 273-1 Kashiwa, Kashiwa, Chiba 277-0005, Japan.
ACS Synth Biol. 2024 Dec 20;13(12):3908-3916. doi: 10.1021/acssynbio.4c00221. Epub 2024 Nov 21.
Ribosome arrest peptides (RAPs) such as the SecM arrest peptide (SecM AP: FSTPVWISQAQGIRAGP) and WPPP with consecutive Pro residues are known to induce translational stalling in . We demonstrate that the translation-enhancing SKIK peptide tag, which consists of four amino acid residues Ser-Lys-Ile-Lys, effectively alleviates translational arrest caused by WPPP. Moreover, the proximity between SKIK and WPPP significantly influences the extent of this alleviation, observed in both PURE cell-free protein synthesis and in vivo protein production systems, resulting in a substantial increase in the yield of proteins containing such RAPs. Furthermore, we unveil that nascent SKIK peptide tag and translation elongation factor P (EF-P) alleviate ribosome stalling in consecutive-Pro-rich protein to synergistically promote translation. A kinetic analysis based on the generation of superfolder green fluorescent protein under in vitro translation reaction reveals that the ribosome turnover is enhanced by more than 10-fold when the SKIK peptide tag is positioned immediately upstream of the SecM AP sequence. Our findings provide valuable insights into optimizing protein production processes, which are essential for advancing synthetic biology applications.
核糖体停滞肽(RAPs),如信号肽酶M停滞肽(SecM AP:FSTPVWISQAQGIRAGP)和含有连续脯氨酸残基的WPPP,已知会在[具体环境未提及]中诱导翻译停滞。我们证明,由四个氨基酸残基Ser-Lys-Ile-Lys组成的增强翻译的SKIK肽标签能有效缓解由WPPP引起的翻译停滞。此外,SKIK与WPPP之间的距离显著影响这种缓解程度,这在无细胞蛋白质合成系统和体内蛋白质生产系统中均有观察到,从而导致含有此类RAPs的蛋白质产量大幅增加。此外,我们还发现新生的SKIK肽标签和翻译延伸因子P(EF-P)能缓解富含连续脯氨酸的蛋白质中的核糖体停滞,协同促进翻译。基于体外翻译反应中超级折叠绿色荧光蛋白的生成进行的动力学分析表明,当SKIK肽标签位于SecM AP序列紧邻上游时,核糖体周转增强了10倍以上。我们的研究结果为优化蛋白质生产过程提供了有价值的见解,这对于推进合成生物学应用至关重要。