首页> 美国卫生研究院文献>Nucleic Acids Research >A synthetic alanyl-initiator tRNA with initiator tRNA properties as determined by fluorescence measurements: comparison to a synthetic alanyl-elongator tRNA.
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A synthetic alanyl-initiator tRNA with initiator tRNA properties as determined by fluorescence measurements: comparison to a synthetic alanyl-elongator tRNA.

机译:具有通过荧光测量确定的引发剂tRNA特性的合成丙氨酰引发剂tRNA:与合成丙氨酰延长剂tRNA的比较。

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摘要

Two synthetic tRNAs have been generated that can be enzymatically aminoacylated with alanine and have AAA anticodons to recognize a poly(U) template. One of the tRNAs (tRNA(eAla/AAA)) is nearly identical to Escherichia coli elongator tRNA(Ala). The other has a sequence similar to Escherichia coli initiator tRNA(Met) (tRNA(iAla/AAA)). Although both tRNAs can be used in poly(U)-directed nonenzymatic initiation at 15 mM Mg2+, only the elongator tRNA can serve for peptide elongation and polyalanine synthesis. Only the initiator tRNA can be bound to 30S ribosomal subunits or 70S ribosomes in the presence of initiation factor 2 (IF-2) and low Mg2+ suggesting that it can function in enzymatic peptide initiation. A derivative of coumarin was covalently attached to the alpha amino group of alanine of these two Ala-tRNA species. The fluorescence spectra, quantum yield and anisotropy for the two Ala-tRNA derivatives are different when they are bound to 70S ribosomes (nonenzymatically in the presence of 15 mM Mg2+) indicating that the local environment of the probe is different. Also, the effect of erythromycin on their fluorescence is quite different, suggesting that the probes and presumably the alanine moiety to which they are covalently linked are in different positions on the ribosomes.
机译:已经产生了两个合成的tRNA,它们可以被丙氨酸酶促氨酰化并具有AAA反密码子以识别poly(U)模板。其中一种tRNA(tRNA(eAla / AAA))与大肠杆菌延伸子tRNA(Ala)几乎相同。另一个具有与大肠杆菌启动子tRNA(Met)(tRNA(iAla / AAA))类似的序列。尽管两个tRNA均可用于15 mM Mg2 +的多聚(U)定向非酶法起始反应,但只有延伸剂tRNA可用于肽延伸和聚丙氨酸合成。在存在起始因子2(IF-2)和低Mg2 +的情况下,只有启动子tRNA可以与30S核糖体亚基或70S核糖体结合,这表明它可以在酶促肽起始中发挥作用。香豆素的衍生物共价附于这两个Ala-tRNA种类的丙氨酸的α氨基上。当两个Ala-tRNA衍生物与70S核糖体结合时(在15 mM Mg2 +存在下非酶促结合),荧光光谱,量子产率和各向异性是不同的,这表明探针的局部环境是不同的。同样,红霉素对其荧光的影响也大不相同,这表明探针以及与它们共价连接的丙氨酸部分在核糖体上的位置不同。

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