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大鼠骨骼肌多核糖体的制备及其某些性质

Preparation and some properties of rat skeletal-muscle polyribosomes.

作者信息

Chen S C, Young V R

出版信息

Biochem J. 1968 Jan;106(1):61-7. doi: 10.1042/bj1060061.

Abstract
  1. A method is described for the sucrose-gradient sedimentation analysis of ribosomes in a post-mitochondrial supernatant of rat skeletal muscle. 2. An essential feature of the method involves the use of buffer of ionic strength 0.3 for homogenization of the muscle tissue. 3. Polyribosomes can be prepared by precipitation from post-mitochondrial supernatant of skeletal muscle by adjustment of the potassium chloride content of the medium. These polyribosomes stimulate cell-free amino acid incorporation in vitro in an energy-dependent system. 4. Ribosome aggregates of uniform size distribution can be obtained by adjustment of the ionic strength of the post-mitochondrial supernatant, followed by differential sucrose-gradient centrifugation. 5. In vivo, rat skeletal-muscle polyribosomes became labelled by (14)C-labelled amino acid within 15min., and radioactivity was associated with the light ribosome species within 45min. 6. Electron microscopy of the polyribosomes revealed aggregations containing more than 40 single ribosomes.
摘要
  1. 本文描述了一种用于大鼠骨骼肌线粒体后上清液中核糖体蔗糖梯度沉降分析的方法。2. 该方法的一个基本特征是使用离子强度为0.3的缓冲液来匀浆肌肉组织。3. 通过调节培养基中氯化钾的含量,可从骨骼肌线粒体后上清液中沉淀制备多核糖体。这些多核糖体在能量依赖系统中能刺激体外无细胞氨基酸掺入。4. 通过调节线粒体后上清液的离子强度,然后进行差速蔗糖梯度离心,可获得大小分布均匀的核糖体聚集体。5. 在体内,大鼠骨骼肌多核糖体在15分钟内被(14)C标记的氨基酸标记,45分钟内放射性与轻核糖体种类相关。6. 多核糖体的电子显微镜检查显示含有40多个单个核糖体的聚集体。

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In vitro amino acid incorporation into myosin by free polysomes of rat skeletal muscle.
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引用本文的文献

本文引用的文献

1
High-Resolution Density Gradient Sedimentation Analysis.高分辨率密度梯度沉降分析。
Science. 1960 Jan 1;131(3392):32-3. doi: 10.1126/science.131.3392.32.
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Messenger-RNA attachment to active ribosomes.信使核糖核酸与活性核糖体的附着
Proc Natl Acad Sci U S A. 1962 Mar 15;48(3):430-6. doi: 10.1073/pnas.48.3.430.
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A multiple ribosomal structure in protein synthesis.蛋白质合成中的多核糖体结构。
Proc Natl Acad Sci U S A. 1963 Jan 15;49(1):122-9. doi: 10.1073/pnas.49.1.122.

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