Multiplexed Organelles Portrait Barcodes for Subcellular MicroRNA Array Detection in Living Cells.
Wei WeiHuiting LuWenhao DaiXiaonan ZhengHaifeng DongPublished in: ACS nano (2022)
Multiplexed profiling of microRNAs' subcellular expression and distribution is essential to understand their spatiotemporal function information, but it remains a crucial challenge. Herein, we report an encoding approach that leverages combinational fluorescent dye barcodes, organelle targeting elements, and an independent quantification signal, termed Multiplexed Organelles Portrait Barcodes (MOPB), for high-throughput profiling of miRNAs from organelles. The MOPB barcodes consist of heterochromatic fluorescent dye-loaded shell-core mesoporous silica nanoparticles modified with organelle targeting peptides and molecular beacon detection probes. Using mitochondria and endoplasmic reticulum as models, we encoded four Cy3/AMCA ER-MOPB and four Cy5/AMCA Mito-MOPB by varying the Cy3 and Cy5 intensity for distinguishing eight organelles' miRNAs. Significantly, the MOPB strategy successfully and accurately profiled eight subcellular organelle miRNAs' alterations in the drug-induced Ca 2+ homeostasis breakdown. The approach should allow more widespread application of subcellular miRNAs and multiplexed subcellular protein biomarkers' monitoring for drug discovery, cellular metabolism, signaling transduction, and gene expression regulation readout.
Keyphrases
- living cells
- single cell
- endoplasmic reticulum
- high throughput
- fluorescent probe
- drug induced
- gene expression
- single molecule
- drug discovery
- liver injury
- label free
- cancer therapy
- loop mediated isothermal amplification
- poor prognosis
- small molecule
- drug delivery
- quantum dots
- highly efficient
- dna methylation
- high intensity
- high resolution
- real time pcr
- amino acid
- long non coding rna
- health information
- high density
- protein kinase