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Author Spotlight: Metallic Nanocomposites to Eliminate Antibiotic-Resistant Bacteria
Published on: October 4, 2024
Chitosan-Functionalized Magnetic Graphene Oxide Nanocomposites Enable High-Purity mRNA Enrichment To Avoid False
Yue Wang1, Jian-Feng Sun1, Heng-Tao Fu1
1State Key Laboratory of Mechanism and Quality of Chinese Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau 999078, China.
Abstract:
Messenger RNA (mRNA) has emerged as a transformative therapeutic frontier, and the discovery of its chemical modifications has revealed critical post-transcriptional regulatory mechanisms. Accurate investigation of these modifications requires ultrapure mRNA, yet conventional isolation methods often suffer from rRNA contamination. To address this issue, we developed chitosan-functionalized magnetic graphene oxide nanocomposites (Fe3O4/GO/CS) engineered with tailored surface properties. The nanocomposites leverage chitosan for steric hindrance against magnetic aggregation and graphene oxide for its ultrahigh surface area, enabling high-density oligo(dT) probe immobilization. The platform achieved specific mRNA capture with markedly reduced rRNA coisolation since the optimized negative zeta potential and surface chemistry preferentially capture linear poly(A)-tailed mRNA over structured rRNA through differential electrostatic and π-π stacking interactions. When applied to total RNA and mitochondrial RNA from PC12 cells, Fe3O4/GO/CS demonstrated 1.5-fold higher mRNA enrichment efficiency compared with commercial kits. Comprehensive validation of the enriched mRNA using a bioanalyzer and agarose gel electrophoresis confirmed a significant reduction of 18S and 28S rRNA contamination by Fe3O4/GO/CS, with residual levels decreasing to below 1%. The resulting high-purity mRNA enabled sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) modification profiling, allowing for accurate quantification of low-abundance mRNA modifications. Additionally, background interference from rRNA modifications (such as 2'-O-methylation) and specific oligonucleotide fragments was significantly reduced, substantially avoiding the risk of false-positive identifications. This novel platform established an effective sample preparation method for mRNA modification analysis, while its expandability to diverse downstream applications provides high-quality mRNA for empowering next-generation mRNA-based diagnostics and therapeutics.
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