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吉田肝癌核糖体解离为活性颗粒。

The dissociation of Yoshida hepatoma ribosomes into active particles.

作者信息

Gravela E

出版信息

Biochem J. 1971 Jan;121(1):145-50. doi: 10.1042/bj1210145.

Abstract
  1. The sedimentation pattern of Yoshida hepatoma ribosomes shows mainly a high dimer peak and an intermediate peak between those of monomer and dimer. 2. The treatment of the postmitochondrial supernatant with EDTA or potassium chloride leads to the dissociation of ribosomes into subunits, through a decrease ofthe ribosomal Mg(2+)/phosphorus ratio. Provided that the deprivation of endogenous Mg(2+) is not complete, the subunits reassociate into active polyribosomes after addition of magnesium chloride to the medium. If the Mg(2+)/phosphorus ratio is lowered below 0.01 (mumol/mumol), structural changes occur, that become evident by a loss of protein and by a decreased sedimentation rate, which render the subribosomal particles unable to reassociate. 3. In the re-formation of polyribosomes from subunits, during the progressive increase of the concentration of magnesium chloride in the medium, the formation of monomeric ribosomes seems to be intermediate. 4. A dimerization of monomers and subunits occurs at concentrations of magnesium chloride greater than those required for the re-formation of polyribosomes and a preincubation for 1h at 0 degrees C is necessary for the maximum dimerization, whereas the complete reconstitution of polyribosomes is immediate.
摘要
  1. 吉田肝癌核糖体的沉降模式主要显示出一个高的二聚体峰以及一个介于单体和二聚体之间的中间峰。2. 用乙二胺四乙酸(EDTA)或氯化钾处理线粒体后上清液,通过降低核糖体的镁离子(Mg²⁺)/磷比率,导致核糖体解离成亚基。倘若内源性镁离子的缺失不完全,向培养基中添加氯化镁后,亚基会重新结合成活性多核糖体。如果镁离子/磷比率降低到低于0.01(微摩尔/微摩尔),就会发生结构变化,这通过蛋白质的损失和沉降速率的降低而变得明显,使得核糖体亚颗粒无法重新结合。3. 在从亚基重新形成多核糖体的过程中,随着培养基中氯化镁浓度的逐渐增加,单体核糖体的形成似乎处于中间阶段。4. 在氯化镁浓度高于重新形成多核糖体所需浓度时,单体和亚基会发生二聚化,并且在0℃预孵育1小时对于最大程度的二聚化是必要的,而多核糖体的完全重建是即时的。

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Ribosomal precursor particles in the HeLa cell nucleus.HeLa细胞核中的核糖体前体颗粒。
J Mol Biol. 1967 Apr 28;25(2):235-51. doi: 10.1016/0022-2836(67)90140-4.

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