| Literature DB >> 34354295 |
Byungjin Hwang1,2,3,4,5, David S Lee1,2, Whitney Tamaki6, Yang Sun1,2, Anton Ogorodnikov1,2, George C Hartoularos1,2,7, Aidan Winters7, Bertrand Z Yeung8, Kristopher L Nazor8, Yun S Song9,10,11, Eric D Chow12, Matthew H Spitzer13,14,15,11, Chun Jimmie Ye16,17,18,19,20,21,22,23.
Abstract
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.Entities:
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Year: 2021 PMID: 34354295 PMCID: PMC8643207 DOI: 10.1038/s41592-021-01222-3
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547