首页> 美国卫生研究院文献>Biochemical Journal >Re-activation of the peptidyltransferase centre of rabbit reticulocyte ribosomes after inactivation by exposure to low concentrations of magnesium ion.
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Re-activation of the peptidyltransferase centre of rabbit reticulocyte ribosomes after inactivation by exposure to low concentrations of magnesium ion.

机译:通过暴露于低浓度的镁离子使其失活后兔网状细胞核糖体的肽基转移酶中心重新激活。

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摘要

1. The larger subrivosomal particles of rabbit reticulocytes retained full activity in the puromycin reaction and in poly(U)-directed polyphenylalanine synthesis after 4h at 0 degrees C when buffered 0.5M-NH4Cl/10-30mM-MgCl2 was the solvent. 2. Activity in the puromycin reaction was diminished to approx 10% after 15-30 min at 0 degrees C when the concentration of MgCl2 was lowered to 2mM. 3. Activity was not restored when the concentration of MgCl2 was raised from 2mM to 10-30 mM at 0 degrees C. However, activity was recovered as measured by both assay systems when the ribosome fraction was heated to 37 degrees C at the higher concentrations of MgCl2. 4. Recovery of activity was noted during the course of the polyphenylalanine synthesis in 50 mM-KCl/5mM-MgCl2/25mM-Tris/HCl, pH 7.6, at 37 degrees C. Re-activation was slow at 20 degrees C and below. 5. No more than about 5% of the protein moiety of the subparticle was lost in 0.5M-NH4Cl on decreasing MgCl2 concentration from 10mM to 2mM. No proteins were detected in the supernatant fractions by gel electrophoresis after ribosomes were separated by differential centrifugation. The supernatant fraction was not essential for the recovery of activity. However, at higher (e.g. 1M) concentrations of NH4Cl, proteins were split from the subparticle. 6. The loss and regain of activity found on lowering and restoring the concentration of MgCl2 at 0.5M-NH4Cl appears to arise from a conformational change that does not seem to be associated with a loss and regain of particular proteins. 7. A 2% decrease in E260 was noticed when the concentration of Mg2+ was restored, and the change in the spectrum indicated a net increase of approx. 100A-U base-pairs per subribosomal particle. 8. When the concentration of Mg2+ was restored, S20,W of the subparticle remained at 52+/- 1S until the sample was incubated at 37 degrees C when S20,W increased to 56 +/- 1S compared with the value of 58 +/- 1S for the subparticle as originally isolated.
机译:1.在0.5M-NH4Cl / 10-30mM-MgCl2缓冲液为溶剂的情况下,在0℃下4h后,兔网织红细胞的较大亚胚体颗粒在嘌呤霉素反应和定向于聚(U)的聚苯丙氨酸合成中保持全部活性。 2.当MgCl2的浓度降低到2mM时,在0摄氏度15-30分钟后,嘌呤霉素反应的活性降低到大约10%。 3.当MgCl2的浓度在0摄氏度下从2mM升高到10-30毫米时,活性没有恢复。但是,当将核糖体级分在较高的浓度下加热到37摄氏度时,两种测定系统都恢复了活性氯化镁。 4.在37℃下,在pH 7.6的50mM-KCl / 5mM-MgCl2 / 25mM-Tris / HCl中,在聚苯丙氨酸合成过程中注意到活性恢复。在20℃及以下,重新活化缓慢。 5.当MgCl2浓度从10mM降低到2mM时,在0.5M-NH4Cl中损失的亚颗粒蛋白质部分的比例不超过5%。在通过差速离心分离核糖体之后,通过凝胶电泳在上清液级分中没有检测到蛋白质。上清液级分对于活性的恢复不是必需的。但是,在较高浓度(例如1M)的NH4Cl中,蛋白质会从亚颗粒中分裂出来。 6.降低和恢复0.5M-NH4Cl中MgCl2的浓度时发现的活性丧失和恢复似乎是由构象变化引起的,该构象变化似乎与特定蛋白质的丧失和恢复无关。 7.当Mg2 +的浓度恢复时,E260下降了2%,光谱的变化表明净增加了约5%。每个核糖体下颗粒100A-U碱基对。 8.当Mg2 +的浓度恢复时,子颗粒的S20,W保持在52 +/- 1S,直到将样品在37°C孵育时,S20,W从58+的值增加到56 +/- 1S。 /-1S为最初分离的亚粒子。

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