Kazemie M
Eur J Biochem. 1976 Aug 16;67(2):373-8. doi: 10.1111/j.1432-1033.1976.tb10701.x.
The activity of 50-S subunits to stimulate the binding of aminoacyl-tRNA to the 30-S subunits was lost when the particles were washed with LiCl concentrations higher than 1.0 M [Kazemie, M. (1975) Eur. J. Biochem. 58,501-510]. The particles could regain this activity when they were incubated with the corresponding LiCl washes. This effect of LiCl washes was used as an assay for identification of 50-S subunit proteins which are essential for binding of aminoacyl-tRNA. A protein mixture containing mainly Ll, Lll and L16 can reactivate 50-S "core" particles, consisting of 10 proteins and 23-S RNA, to bind aminoacyl-tRNAs in the presence of 30-S subunits. Besides 5-S RNA, protein L24 has a stimulatory effect on the binding of aminoacyl-tRNA. Proteins L2, L20 and L23 are possibly required for maintaining the 50-S subunits in the correct conformation for binding of aminoacyl-tRNAs.
当用浓度高于1.0 M的LiCl洗涤颗粒时,50-S亚基刺激氨酰基-tRNA与30-S亚基结合的活性丧失[卡泽米,M.(1975年)《欧洲生物化学杂志》58卷,501 - 510页]。当将颗粒与相应的LiCl洗涤液一起孵育时,它们可以恢复这种活性。LiCl洗涤液的这种作用被用作鉴定对氨酰基-tRNA结合至关重要的50-S亚基蛋白质的一种检测方法。一种主要包含L1、L2和L16的蛋白质混合物可以在30-S亚基存在的情况下,使由10种蛋白质和23-S RNA组成的50-S“核心”颗粒重新激活,以结合氨酰基-tRNA。除了5-S RNA外,蛋白质L24对氨酰基-tRNA的结合有刺激作用。蛋白质L2、L20和L23可能是维持50-S亚基处于与氨酰基-tRNA结合的正确构象所必需的。