Hierarchical DNA branch assembly-encoded fluorescent nanoladders for single-cell transcripts imaging.
Xiaowen CaoFeng ChenJing XueYue ZhaoMin BaiYongxi ZhaoPublished in: Nucleic acids research (2022)
Spatial visualization of single-cell transcripts is limited by signal specificity and multiplexing. Here, we report hierarchical DNA branch assembly-encoded fluorescent nanoladders, which achieve denoised and highly multiplexed signal amplification for single-molecule transcript imaging. This method first offers independent RNA-primed rolling circle amplification without nonspecific amplification based on circular DNAzyme. It then executes programmable DNA branch assembly on these amplicons to encode virtual signals for visualizing numbers of targets by FISH. In theory, more virtual signals can be encoded via the increase of detection spectral channels and repeats of the same sequences on barcode. Our method almost eliminates nonspecific amplification in fixed cells (reducing nonspecific spots of single cells from 16 to nearly zero), and achieves simultaneous quantitation of nine transcripts by using only two detection spectral channels. We demonstrate accurate RNA profiling in different cancer cells, and reveal diverse localization patterns for spatial regulation of transcripts.
Keyphrases
- nucleic acid
- single cell
- single molecule
- living cells
- label free
- rna seq
- high resolution
- high throughput
- atomic force microscopy
- fluorescent probe
- circulating tumor
- induced apoptosis
- optical coherence tomography
- mass spectrometry
- real time pcr
- loop mediated isothermal amplification
- cell cycle arrest
- cell free
- ms ms
- magnetic resonance
- gene expression
- genome wide
- magnetic resonance imaging
- photodynamic therapy
- cell death
- oxidative stress
- signaling pathway
- cell proliferation
- structural basis
- computed tomography