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核糖体蛋白复合物L7/12-L10与蛋白L11和23S RNA 5'-三分之一区域结合的研究:50S亚基的一个功能中心

Studies on the binding of the ribosomal protein complex L7/12-L10 and protein L11 to the 5'-one third of 23S RNA: a functional centre of the 50S subunit.

作者信息

Dijk J, Garrett R A, Müller R

出版信息

Nucleic Acids Res. 1979 Jun 25;6(8):2717-29. doi: 10.1093/nar/6.8.2717.

Abstract

The RNA binding sites of the protein complex of L7/12 dimers and L10, and of protein L11, occur within the 5'-one third of 23S RNA. Binding of the L7/12-L10 protein complex to the 23S RNA is stimulated by protein L11 and vice-versa. This is the second example to be established of mutual stimulation of RNA binding by two ribosomal proteins or protein complexes, and suggests that this may be an important principle governing ribosomal protein-RNA assembly. When the L7/12-L10 complex is bound to the RNA, L10 becomes strongly resistant to trypsin. Since the L7/12 dimer does not bind specifically to the 23S RNA, this suggests that L10 constitutes a major RNA binding site of the protein complex. Only one of the L7/12 dimers is bound strongly in the (L7/12-L10)-23S RNA complex; the other can dissociate with no concurrent loss of L10.

摘要

L7/12二聚体与L10以及蛋白质L11的蛋白质复合物的RNA结合位点位于23S RNA的5'端三分之一区域内。蛋白质L11可刺激L7/12 - L10蛋白质复合物与23S RNA的结合,反之亦然。这是已确定的两个核糖体蛋白质或蛋白质复合物相互刺激RNA结合的第二个例子,表明这可能是指导核糖体蛋白质 - RNA组装的一个重要原则。当L7/12 - L10复合物与RNA结合时,L10对胰蛋白酶具有很强的抗性。由于L7/12二聚体不会特异性地结合23S RNA,这表明L10构成了该蛋白质复合物的主要RNA结合位点。在(L7/12 - L10)- 23S RNA复合物中,只有一个L7/12二聚体紧密结合;另一个可以解离,而L10不会同时丢失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae2/327888/cd743236e9c6/nar00449-0078-a.jpg

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