Reconstitution of yeast translation elongation and termination in vitro utilizing CrPV IRES-containing mRNA
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<jats:title>Abstract</jats:title><jats:p>We developed an in vitro translation system from yeast, reconstituted with purified translation elongation and termination factors and programmed by CrPV IGR IRES-containing mRNA, which functions in the absence of initiation factors. The system is capable of synthesizing the active reporter protein, nanoLuciferase, with a molecular weight of 19 kDa. The protein synthesis by the system is appropriately regulated by controlling its composition, including translation factors, amino acids and antibiotics. We found that a high eEF1A concentration relative to the ribosome concentration is critically required for efficient IRES-mediated translation initiation, to ensure its dominance over IRES-independent random internal translation initiation.</jats:p>
収録刊行物
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- The journal of biochemistry
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The journal of biochemistry 167 (5), 441-450, 2020-05
Tokyo : Japanese Biochemical Society
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詳細情報 詳細情報について
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- CRID
- 1522825130416649728
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- NII論文ID
- 40022226784
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- NII書誌ID
- AA00694073
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- ISSN
- 0021924X
- 17562651
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- NDL書誌ID
- 030402958
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- Web Site
- http://id.ndl.go.jp/bib/030402958
- https://ndlsearch.ndl.go.jp/books/R000000004-I030402958
- http://academic.oup.com/jb/advance-article-pdf/doi/10.1093/jb/mvaa021/32916015/mvaa021.pdf
- http://academic.oup.com/jb/article-pdf/167/5/441/33466228/mvaa021.pdf
- https://search.jamas.or.jp/link/ui/2021087558
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- 本文言語コード
- en
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- NDL 雑誌分類
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- ZR2(科学技術--生物学--生化学)
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- データソース種別
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- NDL
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