Suppr超能文献

红外基质辅助激光解吸/电离质谱中核酸的离子稳定性

Ion stability of nucleic acids in infrared matrix-assisted laser desorption/ionization mass spectrometry.

作者信息

Nordhoff E, Cramer R, Karas M, Hillenkamp F, Kirpekar F, Kristiansen K, Roepstorff P

机构信息

Institute for Medical Physics and Biophysics, University of Münster, Germany.

出版信息

Nucleic Acids Res. 1993 Jul 25;21(15):3347-57. doi: 10.1093/nar/21.15.3347.

Abstract

Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) with infrared laser light of a wavelength of 2.94 microns has been used for the analysis of nucleic acids. Spectra of oligodeoxynucleotides up to 26 nucleotides, oligothymidylic acids up to 100 nucleotides as well as different synthetic RNA oligomers and RNA transcripts up to 104 nucleotides are presented. A main problem in the analysis of oligodeoxynucleotides was found to be related to the loss of bases. The stability of oligothymidylic acids as opposed to oligodeoxynucleotides containing all four bases indicates that the loss of bases is correlated with A, C and G protonation which decreases the stability of the N-glycosidic bond. Experiments indicate that the breakage of the N-glycosidic bond probably occurs during the desorption process due to proton transfer from the phosphodiester groups to the ionizable bases. RNA displayed a significantly higher stability in MALDI-MS due to the presence of a 2'-OH group. Consequently, signals of RNA transcripts with a length of up to 142 nucleotides could be detected by MALDI-MS. Technical details of the method, including the distribution of positive counterions on the phosphodiester backbone, the upper mass limit and mass accuracy are discussed along with a number of potential analytical applications.

摘要

波长为2.94微米的红外激光基质辅助激光解吸/电离质谱(MALDI-MS)已用于核酸分析。文中展示了长达26个核苷酸的寡脱氧核苷酸、长达100个核苷酸的寡胸苷酸以及长达104个核苷酸的不同合成RNA寡聚物和RNA转录本的光谱。研究发现,寡脱氧核苷酸分析中的一个主要问题与碱基丢失有关。与含有所有四种碱基的寡脱氧核苷酸相比,寡胸苷酸的稳定性表明,碱基丢失与A、C和G质子化相关,而这会降低N-糖苷键的稳定性。实验表明,N-糖苷键的断裂可能发生在解吸过程中,原因是质子从磷酸二酯基团转移到可电离碱基上。由于存在2'-OH基团,RNA在MALDI-MS中表现出显著更高的稳定性。因此,MALDI-MS能够检测到长度达142个核苷酸的RNA转录本的信号。文中还讨论了该方法的技术细节,包括磷酸二酯主链上正抗衡离子的分布、质量上限和质量准确度,以及一些潜在的分析应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a10b/331430/e2b14994f3db/nar00064-0023-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验