Reyes R, Vazquez D, Ballesta J P
Eur J Biochem. 1976 Aug 1;67(1):267-74. doi: 10.1111/j.1432-1033.1976.tb10658.x.
Rat liver ribosomes and 60-S ribosome subunits were treated with the primary-amino-group-specific reagent 2-methoxy-5-nitrotropone. Important differences in the sensitivity of several ribosomal activities to inactivation by the reagent were observed. While elongation-factor-dependent activities are totally abolished in the treated particles, peptidyl transferase activity is either unaffected in 60-S ribosomal subunits or even strongly stimulated in 80-S ribosomes. Analysis of the ribosomal proteins modified by nitrotropone made it possible to draw some conclusions on their accessibility in the ribosomal structure and to relate some proteins with their involvement in the ribosome active centers. Thus, proteins L3, L13, L15 and L23 seem to be in a rather well protected position while proteins L10, L35, L37, X1 and X2 are totally exposed to the reagent. The protein accessibility also depends on the ribosome conformation, proteins L14 and L17, for instance, being sensitive in 80-S ribosomes and protected in 60-S subunits. In relation to the implication of proteins in functional centers, the data presented here together with other data obtained from protein-deficient core particles seem to indicate a possible role of proteins L21 and/or L26 in the peptidyl transferase center.
用伯氨基特异性试剂2-甲氧基-5-硝基托品酮处理大鼠肝脏核糖体和60-S核糖体亚基。观察到几种核糖体活性对该试剂失活的敏感性存在重要差异。在处理过的颗粒中,依赖延伸因子的活性完全丧失,而肽基转移酶活性在60-S核糖体亚基中不受影响,在80-S核糖体中甚至受到强烈刺激。对经硝基托品酮修饰的核糖体蛋白进行分析,有助于对其在核糖体结构中的可及性得出一些结论,并将一些蛋白质与其在核糖体活性中心的作用联系起来。因此,蛋白质L3、L13、L15和L23似乎处于相当受保护的位置,而蛋白质L10、L35、L37、X1和X2则完全暴露于该试剂。蛋白质的可及性还取决于核糖体的构象,例如,蛋白质L14和L17在80-S核糖体中敏感,而在60-S亚基中受到保护。关于蛋白质在功能中心的作用,本文提供的数据以及从蛋白质缺陷核心颗粒获得的其他数据似乎表明蛋白质L21和/或L26在肽基转移酶中心可能发挥作用。