评估 RNA 循环效率的分析方法

IF 3 3区生物学 Q2 BIOCHEMICAL RESEARCH METHODS

ELECTROPHORESIS Pub Date : 2024-09-30 DOI:10.1002/elps.202400067

Yali Sun, Anis H. Khimani, Yanhong Tong, Zhi-xiang Lu

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引用次数: 0

摘要

环状 RNA（circRNA）已成为 RNA 疗法中的关键角色。与线性 RNA 不同，circRNA 具有闭环结构，使其具有更高的稳定性和抗降解性。基于核酸酶的策略通过精确裂解和促进共价环状结构的形成，成为合成 circRNA 的主要方法。然而，目前仍缺乏能提供高通量定量分析的分析方法，以促进 circRNA 载体的工程化进程。在报告中，我们详细介绍了表征和评估基于核糖酶的 RNA 环化效率的分析方法。我们的方法将吸引对优化 RNA 环化效率感兴趣的研究人员以及那些专注于探索核糖酶催化活性关键要素的研究人员的注意。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Analytical Methods to Evaluate RNA Circularization Efficiency

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Analytical Methods to Evaluate RNA Circularization Efficiency

Circular RNAs (circRNAs) have emerged as pivotal players in RNA therapeutics. Unlike linear counterparts, circRNAs possess a closed-loop structure, conferring them with enhanced stability and resistance to degradation. Ribozyme-based strategy stands out as the predominant method for synthetic circRNA production, by precisely cleaving and promoting the formation of a covalent circular structure. However, there is still a lack of analytical methods that can provide high-throughput and quantitative analysis to facilitate the circRNA vector engineering process. In the report, we detail analytical methods to characterize and evaluate ribozyme-based RNA circularization efficiency. Our approach will capture the attention of researchers interested in optimizing RNA circularization efficiency, as well as those focused on exploring key elements for ribozyme catalytic activity.

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来源期刊

ELECTROPHORESIS 生物-分析化学

CiteScore

6.30

自引率

13.80%

发文量

244

审稿时长

1.9 months

期刊介绍： ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.