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通过 NETD 串联质谱法分析硫代磷酸酯 RNA。

Phosphorothioate RNA Analysis by NETD Tandem Mass Spectrometry.

机构信息

Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA; Department of Biomolecular Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Department of Biomolecular Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.

出版信息

Mol Cell Proteomics. 2024 Apr;23(4):100742. doi: 10.1016/j.mcpro.2024.100742. Epub 2024 Feb 23.

DOI:10.1016/j.mcpro.2024.100742
PMID:38401707
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11047293/
Abstract

Therapeutic RNAs are routinely modified during their synthesis to ensure proper drug uptake, stability, and efficacy. Phosphorothioate (PS) RNA, molecules in which one or more backbone phosphates are modified with a sulfur atom in place of standard nonbridging oxygen, is one of the most common modifications because of ease of synthesis and pharmacokinetic benefits. Quality assessment of RNA synthesis, including modification incorporation, is essential for drug selectivity and performance, and the synthetic nature of the PS linkage incorporation often reveals impurities. Here, we present a comprehensive analysis of PS RNA via tandem mass spectrometry (MS). We show that activated ion-negative electron transfer dissociation MS/MS is especially useful in diagnosing PS incorporation, producing diagnostic a- and z-type ions at PS linkage sites, beyond the standard d- and w-type ions. Analysis using resonant and beam-type collision-based activation reveals that, overall, more intense sequence ions and base-loss ions result when a PS modification is present. Furthermore, we report increased detection of b- and x-type product ions at sites of PS incorporation, in addition to the standard c- and y-type ions. This work reveals that the gas-phase chemical stability afforded by sulfur alters RNA dissociation and necessitates inclusion of additional product ions for MS/MS of PS RNA.

摘要

治疗性 RNA 在其合成过程中通常会被修饰,以确保药物的摄取、稳定性和疗效。硫代磷酸酯 (PS) RNA 是最常见的修饰物之一,其分子中的一个或多个骨架磷酸酯被硫原子取代,而不是标准的非桥接氧,这是因为其合成容易且具有药代动力学优势。RNA 合成的质量评估,包括修饰物的掺入,对于药物的选择性和性能至关重要,而 PS 键合掺入的合成性质通常会揭示杂质。在这里,我们通过串联质谱 (MS) 对 PS RNA 进行了全面分析。我们表明,活化离子-负电子转移解离 MS/MS 特别有助于诊断 PS 掺入,在 PS 键合位点产生诊断的 a- 和 z-型离子,而不仅仅是标准的 d- 和 w-型离子。使用共振和束流型基于碰撞的激活分析表明,总体而言,当存在 PS 修饰时,会产生更强烈的序列离子和碱基缺失离子。此外,我们报告在 PS 掺入部位检测到更多的 b-和 x-型产物离子,除了标准的 c-和 y-型离子。这项工作表明,硫赋予的气相化学稳定性改变了 RNA 的解离,需要包括更多的产物离子用于 PS RNA 的 MS/MS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/9910d91268ae/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/37cafb9bf3a9/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/9bdc9aa2187c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/8f6d516a9182/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/75a324d86707/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/e6431138d85b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/96c0ea54b0d8/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/9910d91268ae/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/37cafb9bf3a9/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/9bdc9aa2187c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/8f6d516a9182/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/75a324d86707/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/e6431138d85b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/96c0ea54b0d8/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4e/11047293/9910d91268ae/gr6.jpg

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