首页> 外文期刊>Nucleic Acids Research >Discriminating duplex and hairpin oligonucleotides using chemical shifts: application to the anticodon stem-loop of Escherichia coli tRNA(Phe).
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Discriminating duplex and hairpin oligonucleotides using chemical shifts: application to the anticodon stem-loop of Escherichia coli tRNA(Phe).

机译:使用化学位移区分双链和发夹寡核苷酸:应用于大肠杆菌tRNA(Phe)的反密码子茎环。

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摘要

A sensitive NMR spectroscopic method for detection of duplex forms of self-complementary nucleic acid sequences has been implemented. The G.U wobble base pair formed between a (15)N-labeled strand and an unlabeled probe strand is used to identify the duplex. The guanine imino resonance, with its characteristic chemical shift, is detected using a 2D (15)N-(1)H heteronuclear multiple quantum coherence (HMQC) spectrum and provides a sensitive and unambiguous route to hairpin-duplex discrimination. The method has been used to identify the duplex and hairpin forms of an RNA oligonucleotide at concentrations of approximately 20 microM. This method has also been used to rule out possible duplex formation of an RNA oligonucleotide corresponding to the unmodified anticodon stem-loop of Escherichia coli tRNA(Phe) and suggests that this hairpin has a 3 nt loop.
机译:已经实现了用于检测双链形式的自身互补核酸序列的灵敏NMR光谱法。在(15)N标记的链和未标记的探针链之间形成的G.U摆动碱基对用于识别双链体。使用2D(15)N-(1)H异核多量子相干(HMQC)光谱检测鸟嘌呤亚氨基共振及其特征性的化学位移,并为发夹双链体识别提供了灵敏且明确的途径。该方法已用于鉴定浓度约为20 microM的RNA寡核苷酸的双链体和发夹形式。此方法也已被用来排除可能与RNA寡核苷酸tRNA(Phe)的未修饰反密码子茎环相对应的RNA寡核苷酸的双链体形成,并暗示该发夹具有3 nt环。

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