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本文引用的文献

1
The molecular structure of polyadenylic acid.聚腺苷酸的分子结构。
J Mol Biol. 1961 Feb;3:71-86. doi: 10.1016/s0022-2836(61)80009-0.
2
Internal organization of the ribosome.核糖体的内部结构
Nature. 1967 Dec 2;216(5118):864-8. doi: 10.1038/216864a0.
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A possible method for characterizing the secondary structure of ribonucleic acids.一种表征核糖核酸二级结构的可能方法。
Biochem J. 1966 Jul;100(1):146-68. doi: 10.1042/bj1000146.
4
Determination of an upper limit to the phosphorus content of polypeptide chain elongation factor and ribosomal proteins in Escherichia coli.大肠杆菌中多肽链延伸因子和核糖体蛋白磷含量上限的测定。
Biochem Biophys Res Commun. 1971 Aug 6;44(3):579-86. doi: 10.1016/s0006-291x(71)80122-5.
5
On the catalytic center of peptidyl transfer: a part of the 50 S ribosome structure.关于肽基转移的催化中心:50 S核糖体结构的一部分。
Cold Spring Harb Symp Quant Biol. 1969;34:39-48. doi: 10.1101/sqb.1969.034.01.008.
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An infrared study of the conformation of RNA and protein in the ribosome.
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Peptide antibiotic-dinucleotide interactions. Nuclear magnetic resonance investigations of complex formation between actinomycin D and d-pGpC in aqueous solution.肽抗生素 - 二核苷酸相互作用。放线菌素D与d - pGpC在水溶液中形成复合物的核磁共振研究。
Biochemistry. 1974 May 21;13(11):2388-95. doi: 10.1021/bi00708a024.
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Preparation of ribosomal subunits by large-scale zonal centrifugation.通过大规模区带离心法制备核糖体亚基。
Methods Enzymol. 1974;30:349-54. doi: 10.1016/0076-6879(74)30037-7.
9
Frequency dependence of 31P NMR linewidths in sonicated phospholipid vesicles: effects of chemical shift anisotropy.超声处理的磷脂囊泡中31P NMR线宽的频率依赖性:化学位移各向异性的影响
FEBS Lett. 1974 Sep 15;46(1):55-8. doi: 10.1016/0014-5793(74)80333-9.
10
Fluorotyrosine alkaline phosphatase: internal mobility of individual tyrosines and the role of chemical shift anisotropy as a 19F nuclear spin relaxation mechanism in proteins.氟代酪氨酸碱性磷酸酶:单个酪氨酸的内部迁移率以及化学位移各向异性作为蛋白质中¹⁹F核自旋弛豫机制的作用。
J Mol Biol. 1975 Oct 15;98(1):121-53. doi: 10.1016/s0022-2836(75)80105-7.

大肠杆菌核糖体的磷-31核磁共振研究。

Phosphorus-31 NMR studies of E. coli ribosomes.

作者信息

Tritton T R, Armitage I M

出版信息

Nucleic Acids Res. 1978 Oct;5(10):3855-69. doi: 10.1093/nar/5.10.3855.

DOI:10.1093/nar/5.10.3855
PMID:31604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC342715/
Abstract

Phosphorus-31 nuclear magnetic resonance spectra, relaxation times and nuclear Overhauser (NOE) enhancement have been measured for E. coli ribosomes, subunits and rRNA. NOE and T1 experiments reveal that the phosphorus relaxation in this organelle is largely dipolar in origin. Moreover these results imply the presence of internal motion within the RNA chain with a correlation time of about 3-5 x 10(-9) sec. In all cases the predominant resonance is centered at about -1.5 ppm (relative to 85% H3PO4) as expected for a phosphodiester linkage where there is a large degree of double helix. The linewidth narrows by about a factor of four when the ribosomal proteins are removed indicating a substantial immobilization of the RNA when it is assembled into the ribosome. In addition to the phosphodiester resonance, ribosomes also reveal one or two narrower resonances shifted to low field by 1-4 ppm. Based on the observation that these resonances show a pH dependent chemical shift, we assign them to phosphate monoesters i.e. terminal 3' or 5' phosphate groups. These terminal phosphates are due to short oligomers of RNA derived from the terminus of the chain.

摘要

已对大肠杆菌核糖体、亚基和rRNA进行了磷-31核磁共振光谱、弛豫时间和核Overhauser效应(NOE)增强的测量。NOE和T1实验表明,该细胞器中的磷弛豫在很大程度上源于偶极作用。此外,这些结果表明RNA链内部存在相关时间约为3 - 5×10(-9)秒的内部运动。在所有情况下,主要共振峰集中在约-1.5 ppm(相对于85% H3PO4)处,这对于存在大量双螺旋的磷酸二酯键来说是预期的。去除核糖体蛋白后,线宽变窄约四倍,这表明RNA组装到核糖体中时会发生显著的固定。除了磷酸二酯共振峰外,核糖体还显示出一两个向低场移动1 - 4 ppm的较窄共振峰。基于这些共振峰显示出pH依赖性化学位移的观察结果,我们将它们归属于磷酸单酯,即末端3'或5'磷酸基团。这些末端磷酸是由RNA链末端衍生的短寡聚物产生的。