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Studies on ribosome structure and interactions near the m62Am62A sequence.

机译:研究m62Am62A序列附近的核糖体结构及其相互作用。

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摘要

Antibodies raised against N6, N6-dimethyl adenosine were used to study the environment and role of the m62Am62A sequences in the E. coli ribosome. It is observed that this sequence is exposed on the surface of isolated 30S subunits, but becomes inaccessible for IgG interaction upon heat activation. The m62Am62A sequence is also inaccessible for IgG interaction in 70S ribosomes or 30S subunits immediately after dissociation of 70S particles. The presence of IgGs results in a significant inhibition of IF3 binding to unactivated 30S particles. IF3 binding to activated 30S subunits is unaffected by the IgGs. Crosslinking of 30S proteins S18 and S21 with the bifunctional phenylene dimaleimide reagents results in a reduction in the extent of 30S-IgG interaction. From what is already known about the location of S18, S21 and the IF3 binding site, it is suggested that the m62Am62A sequence is located close to the initiator tRNA binding site of the 30S subunit during initiation of protein synthesis.
机译:针对N6,N6-二甲基腺苷的抗体被用来研究m62Am62A序列在大肠杆菌核糖体中的环境和作用。观察到该序列暴露于分离的30S亚基的表面,但是在热激活后变得不可与IgG相互作用。刚解离70S颗粒后,m62Am62A序列也无法在70S核糖体或30S亚基中进行IgG相互作用。 IgG的存在会显着抑制IF3与未激活的30S颗粒的结合。 IF3与活化的30S亚基的结合不受IgG的影响。 30S蛋白S18和S21与双功能亚苯基二马来酰亚胺试剂的交联可降低30S-IgG相互作用的程度。根据关于S18,S21和IF3结合位点的位置的已知信息,建议m62Am62A序列在蛋白质合成起始过程中位于靠近30S亚基的起始tRNA结合位点的位置。

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