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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Manipulating the genetic code for membrane protein production: What have we learnt so far?
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Manipulating the genetic code for membrane protein production: What have we learnt so far?

机译:操纵膜蛋白生产的遗传密码:到目前为止,我们学到了什么?

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摘要

With synthetic gene services, molecular cloning is as easy as ordering a pizza. However choosing the right RNA code for efficient protein production is less straightforward, more akin to deciding on the pizza toppings. The possibility to choose synonymous codons in the gene sequence has ignited a discussion that dates back 50 years: Does synonymous codon use matter? Recent studies indicate that replacement of particular codons for synonymous codons can improve expression in homologous or heterologous hosts, however it is not always successful. Furthermore it is increasingly apparent that membrane protein biogenesis can be codon-sensitive. Single synonymous codon substitutions can influence mRNA stability, mRNA structure, translational initiation, translational elongation and even protein folding. Synonymous codon substitutions therefore need to be carefully evaluated when membrane proteins are engineered for higher production levels and further studies are needed to fully understand how to select the codons that are optimal for higher production.
机译:利用合成基因服务,分子克隆就像订购比萨一样容易。但是,选择正确的RNA代码以高效生产蛋白质的过程却不那么简单,更像决定比萨饼的浇头。在基因序列中选择同义密码子的可能性引发了可追溯到50年前的讨论:同义密码子的使用重要吗?最近的研究表明用同义密码子替换特定密码子可以改善同源或异源宿主中的表达,但是并不总是成功的。此外,越来越明显的是膜蛋白的生物发生可能是密码子敏感的。单个同义密码子替换会影响mRNA稳定性,mRNA结构,翻译起始,翻译延伸甚至蛋白折叠。因此,当膜蛋白被设计用于更高的生产水平时,需要仔细评估同义的密码子替代,并且需要进一步的研究以充分了解如何选择最适合更高产量的密码子。

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