SCITO-seq: single-cell combinatorial indexed cytometry sequencing.
Byungjin HwangDavid S LeeWhitney TamakiYang SunAnton OgorodnikovGeorge C HartoularosAidan WintersBertrand Z YeungKristopher L NazorYun S SongEric D ChowMatthew H SpitzerChun Jimmie YePublished in: Nature methods (2021)
The development of DNA-barcoded antibodies to tag cell surface molecules has enabled the use of droplet-based single-cell sequencing (dsc-seq) to profile protein abundances from thousands of cells simultaneously. As compared to flow and mass cytometry, the high per cell cost of current dsc-seq-based workflows precludes their use in clinical applications and large-scale pooled screens. Here, we introduce SCITO-seq, a workflow that uses splint oligonucleotides (oligos) to enable combinatorially indexed dsc-seq of DNA-barcoded antibodies from over 105 cells per reaction using commercial microfluidics. By encoding sample barcodes into splint oligos, we demonstrate that multiplexed SCITO-seq produces reproducible estimates of cellular composition and surface protein expression comparable to those from mass cytometry. We further demonstrate two modified splint oligo designs that extend SCITO-seq to achieve compatibility with commercial DNA-barcoded antibodies and simultaneous expression profiling of the transcriptome and surface proteins from the same cell. These results demonstrate SCITO-seq as a flexible and ultra-high-throughput platform for sequencing-based single-cell protein and multimodal profiling.
Keyphrases
- single cell
- rna seq
- high throughput
- induced apoptosis
- single molecule
- circulating tumor
- cell free
- cell cycle arrest
- genome wide
- mesenchymal stem cells
- cell surface
- endoplasmic reticulum stress
- high resolution
- nucleic acid
- oxidative stress
- randomized controlled trial
- signaling pathway
- electronic health record
- small molecule
- bone marrow
- protein protein
- cell death
- cell therapy
- cell proliferation
- finite element analysis