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用还原烷基化法对核糖体蛋白进行放射性标记及其在研究核糖体-胞质溶胶相互作用中的应用。

Radioactive labelling of ribosomal proteins with reductive alkylation and its use in studying ribosome-cytosol interactions.

作者信息

Kelly C J, Johnson T C

出版信息

Biochem J. 1976 Dec 15;160(3):427-32. doi: 10.1042/bj1600427.

Abstract

Mouse brain ribosomes were radioactively labelled by a cell-free reductive alkylation reaction with NaBH4 and [14C]formaldehyde. The radioactivity was largely associated with ribosomal proteins, but little, if any, of the rRNA was radioactive after the alkylation procedure. Both ribosomal structural proteins and loosely associated components were successfully labelled by this procedure. The sedimentation properties of the ribosomes were unaltered and their ability to carry out poly(U)-directed protein synthesis, although decreased, was largely retained. Incubation of 14C-labelled ribosomes with brain cytosol resulted in a 17% loss of radioactivity, although treatment of the ribosomes with 1.0 m-KCl to remove the loosely associated factors rendered the ribonucleoprotein particles resistant to cytosol effects. The ribosome-cytosol interactions did not appear to be related to an exchange process, since the released radioactivity was largely degraded to acid-soluble material. In addition, the incubation of native ribosomes with brain cytosol resulted in an almost complete loss in the ability of the ribosomes to participate in cell-free protein synthesis.

摘要

通过用硼氢化钠(NaBH4)和[14C]甲醛进行无细胞还原烷基化反应,对小鼠脑核糖体进行放射性标记。放射性主要与核糖体蛋白相关,但在烷基化过程后,很少(如果有的话)rRNA具有放射性。核糖体结构蛋白和松散结合的成分均通过该程序成功标记。核糖体的沉降特性未改变,其进行聚(U)指导的蛋白质合成的能力虽然有所下降,但大部分得以保留。将14C标记的核糖体与脑细胞质共同孵育导致放射性损失17%,尽管用1.0 m-KCl处理核糖体以去除松散结合的因子使核糖核蛋白颗粒对细胞质的作用具有抗性。核糖体-细胞质相互作用似乎与交换过程无关,因为释放的放射性大部分降解为酸溶性物质。此外,天然核糖体与脑细胞质共同孵育导致核糖体参与无细胞蛋白质合成的能力几乎完全丧失。

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本文引用的文献

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Reductive alkylation of amino groups in proteins.蛋白质中氨基的还原烷基化作用。
Biochemistry. 1968 Jun;7(6):2192-201. doi: 10.1021/bi00846a023.
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The use of proteolytic enzymes in the study of ribosomal structure.蛋白水解酶在核糖体结构研究中的应用。
Biochim Biophys Acta. 1968 Feb 19;154(2):376-87. doi: 10.1016/0005-2795(68)90052-4.

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