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大肠杆菌5S核糖核酸的荧光修饰

Fluorescence modification of Escherichia coli 5S RNA.

作者信息

Digweed M, Erdmann V A, Odom O W, Hardesty B

出版信息

Nucleic Acids Res. 1981 Jul 10;9(13):3187-98. doi: 10.1093/nar/9.13.3187.

Abstract

Reaction of 5S RNA with chlorocetaldehyde leads to the conversion of unpaired adenines to the fluorescent 1,N6-etheno-adenine derivatives. Up to 16 of the 23 adenines in free 5S RNA can be modified, the fastest reacting are A29, A34, A57-59. Partial modification of adenines in this area results in a 20% reduction in the efficiency of 5S RNA incorporation into 50S subunits during reconstitution and a 15% reduction in the activity of these subunits in peptide synthesis. Fluorescence from 1,N6-etheno-adenine is quenched in free 5S RNA and is not detectably further influenced by the binding of proteins E-L5, E-L18 and E-L25, nor by the first stage of the two step E. coli 50S subunit reconstitution procedure. However, the fluorescence is further reduced to near zero after the second step of the reconstitution. Thus, 5S RNS free in solution contains 16 unpaired adenines, those in the region between A29 and A59 particularly accessible to modification by chlorocetaldehyde. This portion of the 5S RNA molecule appears to undergo either a conformational change or interacts with other ribosomal components in the last stage of subunit reassembly.

摘要

5S RNA与氯乙醛反应会导致未配对的腺嘌呤转化为荧光性的1,N6-乙撑腺嘌呤衍生物。游离5S RNA的23个腺嘌呤中多达16个可被修饰,反应最快的是A29、A34、A57 - 59。该区域腺嘌呤的部分修饰会导致在重组过程中5S RNA掺入50S亚基的效率降低20%,以及这些亚基在肽合成中的活性降低15%。1,N6-乙撑腺嘌呤的荧光在游离5S RNA中被淬灭,并且不受蛋白质E-L5、E-L18和E-L25的结合影响,也不受大肠杆菌50S亚基两步重组过程第一步的影响。然而,在重组的第二步之后,荧光进一步降低至接近零。因此,溶液中游离的5S RNS含有16个未配对的腺嘌呤,A29和A59之间区域的腺嘌呤特别容易被氯乙醛修饰。5S RNA分子的这一部分似乎在亚基重新组装的最后阶段经历了构象变化或与其他核糖体成分相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d62/327341/6c87ca37b8c2/nar00406-0208-a.jpg

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