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翻译增强型新生SKIK肽对含连续脯氨酸的抑制肽的影响。

Effect of Translation-Enhancing Nascent SKIK Peptide on the Arrest Peptides Containing Consecutive Proline.

作者信息

Nishikawa Yuma, Fujikawa Riko, Nakano Hideo, Kanamori Takashi, Ojima-Kato Teruyo

机构信息

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.

出版信息

ACS Synth Biol. 2024 Dec 20;13(12):3908-3916. doi: 10.1021/acssynbio.4c00221. Epub 2024 Nov 21.

DOI:10.1021/acssynbio.4c00221
PMID:39573840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11669330/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/6c7af9587fcb/sb4c00221_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/f6eee05c6f50/sb4c00221_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/3d9d0c8a68e2/sb4c00221_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/5e0ea4e88878/sb4c00221_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/6c7af9587fcb/sb4c00221_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/f6eee05c6f50/sb4c00221_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/3d9d0c8a68e2/sb4c00221_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/5e0ea4e88878/sb4c00221_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a37/11669330/6c7af9587fcb/sb4c00221_0004.jpg

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本文引用的文献

1
Nonspecific N-terminal tetrapeptide insertions disrupt the translation arrest induced by ribosome-arresting peptide sequences.非特异性 N 端四肽插入破坏核糖体阻断肽序列诱导的翻译阻断。
J Biol Chem. 2024 Jun;300(6):107360. doi: 10.1016/j.jbc.2024.107360. Epub 2024 May 11.
2
Nascent MSKIK peptide cancels ribosomal stalling by arrest peptides in Escherichia coli.新生的 MSKIK 肽在大肠杆菌中通过阻遏肽取消核糖体的停滞。
J Biol Chem. 2023 May;299(5):104676. doi: 10.1016/j.jbc.2023.104676. Epub 2023 Apr 5.
3
renz: An R package for the analysis of enzyme kinetic data.
renz:用于酶动力学数据分析的 R 包。
BMC Bioinformatics. 2022 May 16;23(1):182. doi: 10.1186/s12859-022-04729-4.
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Folding of VemP into translation-arresting secondary structure is driven by the ribosome exit tunnel.VemP 折叠成翻译阻断的二级结构是由核糖体出口隧道驱动的。
Nucleic Acids Res. 2022 Feb 28;50(4):2258-2269. doi: 10.1093/nar/gkac038.
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Regulation of RNA stability at the 3' end.RNA 稳定性的 3' 端调控。
Biol Chem. 2020 Nov 27;402(4):425-431. doi: 10.1515/hsz-2020-0325. Print 2021 Mar 26.
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Developing a codon optimization method for improved expression of recombinant proteins in actinobacteria.开发一种密码子优化方法,以提高放线菌中重组蛋白的表达水平。
Sci Rep. 2019 Jun 6;9(1):8338. doi: 10.1038/s41598-019-44500-z.
7
A chemical kinetic basis for measuring translation initiation and elongation rates from ribosome profiling data.从核糖体图谱数据中测量翻译起始和延伸速率的化学动力学基础。
PLoS Comput Biol. 2019 May 23;15(5):e1007070. doi: 10.1371/journal.pcbi.1007070. eCollection 2019 May.
8
The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation.核糖体干扰、密码子使用和出口隧道相互作用对翻译延伸速率变化的影响。
PLoS Genet. 2018 Jan 16;14(1):e1007166. doi: 10.1371/journal.pgen.1007166. eCollection 2018 Jan.
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Identification and characterization of a translation arrest motif in VemP by systematic mutational analysis.通过系统的突变分析鉴定和表征 VemP 中的翻译停滞基序。
J Biol Chem. 2018 Feb 23;293(8):2915-2926. doi: 10.1074/jbc.M117.816561. Epub 2018 Jan 9.
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Structural Basis for Polyproline-Mediated Ribosome Stalling and Rescue by the Translation Elongation Factor EF-P.多聚脯氨酸介导的核糖体停滞和翻译延伸因子 EF-P 拯救的结构基础。
Mol Cell. 2017 Nov 2;68(3):515-527.e6. doi: 10.1016/j.molcel.2017.10.014.