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用于通过基质辅助激光解吸/电离飞行时间质谱分析寡核苷酸的简化样品制备方法。

Simplified sample preparation for the analysis of oligonucleotides by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry.

作者信息

Langley G J, Herniman J M, Davies N L, Brown T

机构信息

Department of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, UK.

出版信息

Rapid Commun Mass Spectrom. 1999;13(17):1717-23. doi: 10.1002/(SICI)1097-0231(19990915)13:17<1717::AID-RCM704>3.0.CO;2-R.

Abstract

Matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOFMS) for the analyses of oligonucleotides has generally been carried out using negative ionisation conditions, usually following ammonium ion-exchange chromatography and the addition of ammonium buffers to the MALDI matrix. The molecular ion region is complex, due to the varying degrees of ammoniation of the phosphate backbone of the oligonucleotide. This gives rise to an overall decrease in sensitivity compared with similar size peptides and can cause ambiguity of assignment of the relative molecular mass of the sample. This study describes the use of H(+) ion exchange resin in situ as the means of removing alkali metal ions from the phosphate backbone of the oligonucleotide. An increase in resolution, sensitivity and identification of the molecular species is reported, with little or no difference in sensitivity observed between positive or negative ionisation spectra. This method is now used for routine screening of synthetic oligonucleotides with a gain in sensitivity of 1-2 orders of magnitude compared with previous methods, and mass assignment errors of +/-0.1% are routinely recorded for externally calibrated data.

摘要

用于寡核苷酸分析的基质辅助激光解吸/电离飞行时间质谱(MALDI-TOFMS)通常在负离子化条件下进行,通常是在铵离子交换色谱之后,并向MALDI基质中添加铵缓冲液。由于寡核苷酸磷酸骨架的氨化程度不同,分子离子区域很复杂。与类似大小的肽相比,这导致灵敏度总体下降,并可能导致样品相对分子质量的归属不明确。本研究描述了使用原位H(+)离子交换树脂作为从寡核苷酸磷酸骨架中去除碱金属离子的方法。据报道,分辨率、灵敏度和分子种类的鉴定有所提高,正离子化或负离子化光谱之间的灵敏度几乎没有差异。该方法现在用于合成寡核苷酸的常规筛选,与以前的方法相比,灵敏度提高了1-2个数量级,对于外部校准数据,质量归属误差通常记录为+/-0.1%。

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