1307:片段分析仪系统对长IVT mRNA片段的评估

Kyle D. Luttgeharm, Solange Borg, C. Pocernich
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引用次数: 0

摘要

长段体外转录(IVT) RNA的质量控制分析是具有挑战性的,因为缺乏商用试剂盒来测定超过6000 nt的RNA大小,因此,为了分析长段体外转录RNA, Agilent 5200片段分析仪开发了一种扩展的分离方法,使用商用RNA阶梯。使用RiboMAX大规模RNA生产系统(Promega)生产IVT mRNA。长度为9,000和10,000 nt的RNA转录本在无核酸酶的水中稀释,并使用Agilent RNA试剂盒(15 nt) (p/n DNF-471)在Agilent 5200片段分析仪系统上进行以下修改。Lonza RNA标记物(Lonza) (long RNA Ladder)代替Agilent RNA Ladder,用无核酸酶水稀释至96 ng/μL。根据RNA试剂盒方案,将长RNA梯加入Agilent RNA稀剂标记物(15 nt) (p/n DNF-369-0004)。对于大于6000 nt的片段,在Agilent 5200 Fragment Analyzer软件中,将RNA试剂盒(15 nt)的标准分离方法(8 kV, 45分钟)手动更改为扩展RNA方法(4 kV, 90分钟)。随后的所有运行均采用带有长RNA阶梯的扩展RNA方法。与标准方法相比,扩展方法分离的长RNA阶梯显示出更高的分辨率,这可以从阶梯峰之间的间距增加和9,000 nt峰的清晰度增加中看出。与标准RNA方法(8.4%)相比,扩展RNA方法在试剂盒的整个浓度范围内报告了较低的平均施胶百分比误差(- 0.7%),用于9000 nt样品。在整个稀释系列中,两种分离方法的10,000 nt IVT mRNA平均百分比大小误差相似。使用扩展方法,成功分析了9,000和10,000 nt IVT mRNA样品,具有良好的尺寸精度和准确性,表明商用RNA阶梯可以与片段分析仪系统一起使用,以提供大型IVT mRNA样品的准确尺寸。当需要非常准确的大小或高分辨率来确定IVT mRNA样品中长度超过6,000 nt的不完全转录的降解或大小差异的存在时,推荐使用扩展RNA方法。不适用于诊断程序。引文格式:Kyle D. Luttgeharm, Solange Borg, Chava Pocernich。片段分析仪系统对长IVT mRNA片段的评估[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):1307。
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Abstract 1307: Assessment of long IVT mRNA fragments with the Fragment Analyzer system
Quality control analysis of long in vitro transcribed (IVT) RNAs is challenging due to the lack of commercially available kits for sizing RNA over 6,000 nt, thus, to analyze long IVT RNAs, an extended separation method was developed for the Agilent 5200 Fragment Analyzer using a commercially available RNA ladder. IVT mRNA was produced using the RiboMAX Large Scale RNA Production System (Promega). RNA transcripts 9,000 and 10,000 nt in length were diluted in nuclease-free water and separated on the Agilent 5200 Fragment Analyzer system with the Agilent RNA kit (15 nt) (p/n DNF-471) with the following modifications. The Lonza RNA marker (Lonza) (long RNA Ladder) replaced the Agilent RNA Ladder and was diluted in nuclease-free water to 96 ng/μL. The long RNA Ladder was added to the Agilent RNA Diluent Marker (15 nt) (p/n DNF-369-0004) according to the RNA kit protocol. The standard separation method (8 kV for 45 minutes) for the RNA kit (15 nt) was manually altered to the extended RNA method (4 kV for 90 minutes) in the Agilent 5200 Fragment Analyzer software for fragments greater than 6,000 nt. The extended RNA method with the long RNA Ladder was employed for all subsequent runs. The long RNA Ladder separated with the extended method displayed enhanced resolution compared to separation with the standard method as seen by the increased spacing between the ladder peaks and the increased sharpness of the 9,000 nt peak. The extended RNA method reported a lower average sizing percent error (-0.7 %) over the entire concentration range of the kit compared to the standard RNA method (8.4 %) for the 9,000 nt sample. The 10,000 nt IVT mRNA average percent sizing error was similar between the two separation methods throughout the dilution series. Using the extended method, the 9,000 and 10,000 nt IVT mRNA samples were successfully analyzed with good sizing precision and accuracy, demonstrating that a commercially available RNA ladder can be used with the Fragment Analyzer system to provide accurate sizing of large IVT mRNA samples. The extended RNA method is recommended when extremely accurate sizing or high resolution is needed for determining the presence of degradation or sizing differences from incomplete transcription in IVT mRNA samples longer than 6,000 nt. For Research Use Only. Not for use in diagnostic procedures. Citation Format: Kyle D. Luttgeharm, Solange Borg, Chava Pocernich. Assessment of long IVT mRNA fragments with the Fragment Analyzer system [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 1307.
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