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利用场非对称波形离子淌度和电化学洗脱液相色谱技术扩展表观转录组 RNA 测序和修饰图谱质谱工具箱。

Expanding the Epitranscriptomic RNA Sequencing and Modification Mapping Mass Spectrometry Toolbox with Field Asymmetric Waveform Ion Mobility and Electrochemical Elution Liquid Chromatography.

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6243, United States.

Epigenetic Institute and Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6243, United States.

出版信息

Anal Chem. 2023 Mar 28;95(12):5187-5195. doi: 10.1021/acs.analchem.2c04114. Epub 2023 Mar 14.

DOI:10.1021/acs.analchem.2c04114
PMID:36916610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10190205/
Abstract

Post-transcriptional modifications of RNA strongly influence the RNA structure and function. Recent advances in RNA sequencing and mass spectrometry (MS) methods have identified over 140 of these modifications on a wide variety of RNA species. Most next-generation sequencing approaches can only map one RNA modification at a time, and while MS can assign multiple modifications simultaneously in an unbiased manner, MS cannot accurately catalog and assign RNA modifications in complex biological samples due to limitations in the fragment length and coverage depth. Thus, a facile method to identify novel RNA modifications while simultaneously locating them in the context of their RNA sequences is still lacking. We combined two orthogonal modes of RNA ion separation before MS identification: high-field asymmetric ion mobility separation (FAIMS) and electrochemically modulated liquid chromatography (EMLC). FAIMS RNA MS increases both coverage and throughput, while EMLC LC-MS orthogonally separates RNA molecules of different lengths and charges. The combination of the two methods offers a broadly applicable platform to improve the length and depth of MS-based RNA sequencing while providing contextual access to the analysis of RNA modifications.

摘要

RNA 的转录后修饰强烈影响 RNA 的结构和功能。最近在 RNA 测序和质谱 (MS) 方法方面的进展已经在多种 RNA 物种上鉴定出了超过 140 种修饰。大多数下一代测序方法一次只能映射一种 RNA 修饰,而 MS 可以以无偏倚的方式同时分配多个修饰,但由于片段长度和覆盖深度的限制,MS 无法准确地对复杂生物样本中的 RNA 修饰进行编目和分配。因此,仍然缺乏一种能够在鉴定新的 RNA 修饰的同时,在 RNA 序列的背景下定位它们的简便方法。我们在 MS 鉴定之前结合了两种正交的 RNA 离子分离模式:高场非对称离子淌度分离 (FAIMS) 和电化学调制液相色谱 (EMLC)。FAIMS RNA MS 提高了覆盖率和通量,而 EMLC LC-MS 则正交分离了不同长度和电荷的 RNA 分子。两种方法的结合为提高基于 MS 的 RNA 测序的长度和深度提供了一个广泛适用的平台,同时为 RNA 修饰的分析提供了上下文访问。

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