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首页> 外文期刊>Journal of the American Chemical Society >New Macrocyclic Terbium(iii) Complex For Use In Rna Footprinting Experiments
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New Macrocyclic Terbium(iii) Complex For Use In Rna Footprinting Experiments

机译:用于Rna足迹实验的新型大环Ter(iii)配合物

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摘要

Reaction of terbium triflate with a heptadentate ligand derivative of cyclen, L1 = 2-[7-ethyl-4,10-bis(isopropylcarbamoylmethyl)-1,4,7,10-tetraazacyclododec-1-yl]-N-isopropyl-acetamide, produced a new synthetic ribonuclease, [Tb(L1)(OTf)(OH_2)](OTf)_2-MeCN (C1). X-ray crystal structure analysis indicates that the terbium(III) center in C1 is 9-coordinate, with a capped square-antiprism geometry. While the terbium(III) center is tightly bound by the L1 ligand, two of the coordination sites are occupied by labile water and triflate ligands. In water, the triflate ligand is likely to be displaced, forming [Tb(L1)(OH_2)_2]~(3+), which is able to effectively promote RNA cleavage. This complex greatly accelerates the rate of intramolecular transesterification of an activated model RNA phosphodiester, uridine-3'-p-nitrophenylphos-phate (UpNP), with k_(obs) = 5.5(1) × 10~(-2) s~(-1) at 21 ℃ and pH 7.5, corresponding to an apparent second-order rate constant of 277(5) M~(-1)s~(-1). By contrast, the analogous complex of an octadentate derivative of cyclen featuring only a single labile coordination site, [Tb(L2)(OH_2)](OTf)_3 (C2), where L2 = 2-[4,7,10-tris(isopropylcarbamoylmethyl)-1,4,7,10-tetraazacyclododec-1-yl]-N-isopropyl-acetamide, is inactive. [Tb(L1)(OH_2)_2]~(3+) is also capable of hydrolyzing short transcripts of the HIV-1 transactivation response (TAR) element, HIV-1 dimerization initiation site (DIS) and ribosomal A-site, as well as formyl methionine tRNA (tRNA~(fMet)), albeit at a considerably slower rate than UpNP transesterification (k_(obs) = 2.78(8) × 10~(-5) s~(-1) for TAR cleavage at 37℃, pH 6.5, corresponding to an apparent second-order rate constant of 0.56(2) M~(-1)s~(-1)). Cleavage is concentrated at the single-stranded "bulge" regions of these RNA motifs. Exploiting this selectivity, [Tb(L1)(OH_2)_2]~(3+) was successfully employed in footprinting experiments, in which binding of the Tat peptide and neomydn B to the bulge region of the TAR stem-loop was confirmed.
机译:三氟甲磺酸ter与周期数七齿配体衍生物的反应,L1 = 2- [7-乙基-4,10-双(异丙基氨基甲酰基甲基)-1,4,7,10-四氮杂环十二烷基-1-基] -N-异丙基乙酰胺,生产了一种新的合成核糖核酸酶[Tb(L1)(OTf)(OH_2)](OTf)_2-MeCN(C1)。 X射线晶体结构分析表明,C1中的((III)中心为9坐标,具有方形反棱镜的几何形状。 the(III)中心被L1配体紧密结合,而两个配位位点则被不稳定的水和三氟甲磺酸盐配体占据。在水中,三氟甲磺酸盐配体很可能被置换,形成[Tb(L1)(OH_2)_2]〜(3+),能够有效地促进RNA裂解。该复合物极大地加速了激活的模型RNA磷酸二酯尿苷3'-对硝基苯基磷酸酯(UpNP)的分子内酯交换速率,k_(obs)= 5.5(1)×10〜(-2)s〜( -1)在21℃和pH 7.5下,对应的表观二级速率常数为277(5)M〜(-1)s〜(-1)。相比之下,Cyclone的八齿衍生物的类似络合物仅具有一个不稳定的配位点[Tb(L2)(OH_2)](OTf)_3(C2),其中L2 = 2- [4,7,10-tris (异丙基氨基甲酰基甲基)-1,4,7,10-四氮杂环十二烷基-1-基] -N-异丙基-乙酰胺是不活泼的。 [Tb(L1)(OH_2)_2]〜(3+)还能够水解HIV-1反式激活反应(TAR)元件,HIV-1二聚化起始位点(DIS)和核糖体A位点的短转录本,以及甲硫基甲硫氨酸tRNA(tRNA〜(fMet)),尽管与UpNP酯交换反应的速率相比要慢得多(k_(obs)= 2.78(8)×10〜(-5)s〜(-1)对于TAR在37的裂解率) ,pH 6.5,对应的表观二阶速率常数为0.56(2)M〜(-1)s〜(-1))。切割集中在这些RNA基序的单链“凸起”区域。利用这种选择性,[Tb(L1)(OH_2)_2]〜(3+)被成功用于足迹实验,其中证实了Tat肽和neomydn B与TAR茎环的突出区域结合。

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