首页> 外文期刊>Nucleic Acids Research >Sequencing RNA by a combination of exonuclease digestion and uridine specific chemical cleavage using MALDI-TOF.
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Sequencing RNA by a combination of exonuclease digestion and uridine specific chemical cleavage using MALDI-TOF.

机译:结合核酸外切酶消化和尿苷特异性化学裂解,使用MALDI-TOF对RNA进行测序。

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摘要

The determination of DNA sequences by partial exonuclease digestion followed by Matrix-Assisted Laser Desorption Time of Flight Mass Spectrometry (MALDI-TOF) is a well established method. When the same procedure is applied to RNA, difficulties arise due to the small (1 Da) mass difference between the nucleotides U and C, which makes unambiguous assignment difficult using a MALDI-TOF instrument. Here we report our experiences with sequence specific endonucleases and chemical methods followed by MALDI-TOF to resolve these sequence ambiguities. We have found chemical methods superior to endonucleases both in terms of correct specificity and extent of sequence coverage. This methodology can be used in combination with exonuclease digestion to rapidly assign RNA sequences.
机译:通过部分核酸外切酶消化,然后通过基质辅助激光解吸飞行时间质谱仪(MALDI-TOF)确定DNA序列是一种完善的方法。当对RNA进行相同的操作时,由于核苷酸U和C之间的质量差很小(1 Da),因此会出现困难,这使得使用MALDI-TOF仪器进行明确分配变得困难。在这里,我们报告了我们在序列特异性核酸内切酶和化学方法方面的经验,以及随后的MALDI-TOF解决这些序列歧义性的经验。我们发现在正确的特异性和序列覆盖范围方面,化学方法均优于核酸内切酶。该方法可与核酸外切酶消化结合使用,以快速分配RNA序列。

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