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核糖体结合新生多肽的酶活性。

Enzymatic activity of the ribosome-bound nascent polypeptide.

作者信息

Makeyev E V, Kolb V A, Spirin A S

机构信息

Institute of Protein Research, Russian Academy of Sciences, Pushchino, Moscow Region, Russian Federation.

出版信息

FEBS Lett. 1996 Jan 8;378(2):166-70. doi: 10.1016/0014-5793(95)01438-1.

Abstract

Firefly luciferase was shown to be completely folded and thus enzymatically active immediately upon release from the ribosome [Kolb et al. (1994) EMBO J. 13, 3631-3637]. However, no luciferase activity was observed while full-length luciferase was attached to the ribosome as a peptidyl-tRNA, probably because the C-terminal portion of the enzyme is masked by the ribosome and/or ribosome-associated proteins. Here we have demonstrated that the ribosome-bound enzyme acquires the enzymatic activity when its C-terminus is extended by at least 26 additional amino acid residues. The results demonstrate that the acquisition of the final native conformation by a nascent protein does not need the release of the protein from the ribosome.

摘要

萤火虫荧光素酶在从核糖体释放后立即呈现完全折叠状态,因而具有酶活性[科尔布等人(1994年),《欧洲分子生物学组织杂志》13卷,3631 - 3637页]。然而,当全长荧光素酶作为肽基 - tRNA附着在核糖体上时,未观察到荧光素酶活性,这可能是因为该酶的C末端部分被核糖体和/或核糖体相关蛋白所掩盖。在此我们证明,当核糖体结合的酶的C末端至少额外延伸26个氨基酸残基时,它会获得酶活性。结果表明,新生蛋白质获得最终天然构象并不需要从核糖体上释放。

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