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核糖体亚基结合机制:以寡脱氧核苷酸作为探针

Mechanism of ribosomal subunit association: oligodeoxynucleotides as probes.

作者信息

Agrawal R K, De A, Burma D P

机构信息

Molecular Biology Unit, Banaras Hindu University, Varanasi.

出版信息

Indian J Biochem Biophys. 1992 Apr;29(2):148-53.

PMID:1398707
Abstract

From the kethoxal treatment data [Herr, W.; Chapman, N.M.; Noller, H.F. (1979) J. Mol. Biol. 130, 433-439] some regions of ribosomal RNAs are thought to be responsible for the association of 30S and 50S ribosomes of E. coli to form 70S ribosomes. In order to test this possibility about a dozen oligodeoxynucleotides complementary to the suspected regions of rRNAs were synthesised. Their association with ribosomes and naked rRNAs was tested by the gel filtration technique. In order to check the effects on the ribosomal subunit association or rRNA association either intact 30S and 50S ribosomes or naked 16S and 23S rRNAs were preincubated with the individual oligodeoxynucleotide and its effect was checked by density gradient centrifugation followed by UV absorbance monitoring. Some oligodeoxynucleotides interfered with either subunit association or 16S RNA and 23S RNA association, some with both. These data clearly indicate that RNA-RNA interaction plays the major role in ribosomal subunit association.

摘要

从乙二醛处理数据[赫尔,W.;查普曼,N.M.;诺勒,H.F.(1979年)《分子生物学杂志》130卷,433 - 439页]可知,核糖体RNA的某些区域被认为负责大肠杆菌30S和50S核糖体结合形成70S核糖体。为了验证这种可能性,合成了大约十二种与rRNA的可疑区域互补的寡脱氧核苷酸。通过凝胶过滤技术测试了它们与核糖体和裸露rRNA的结合情况。为了检查对核糖体亚基结合或rRNA结合的影响,将完整的30S和50S核糖体或裸露的16S和23S rRNA与单个寡脱氧核苷酸进行预孵育,并通过密度梯度离心,随后进行紫外吸收监测来检查其效果。一些寡脱氧核苷酸干扰亚基结合或16S RNA与23S RNA的结合,有些则两者都干扰。这些数据清楚地表明,RNA - RNA相互作用在核糖体亚基结合中起主要作用。

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