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Proteins are the primary effectors of cellular function, including cellular metabolism, structural dynamics, and information processing. However, quantitative characterization of proteins at the single-cell level is challenging due to the tiny amount of protein available. Here, we present Abseq, a method to detect and quantitate proteins in single cells at ultrahigh throughput. Like flow and mass cytometry, Abseq uses specific antibodies to detect epitopes of interest; however, unlike these methods, antibodies are labeled with sequence tags that can be read out with microfluidic barcoding and DNA sequencing. We demonstrate this novel approach by characterizing surface proteins of different cell types at the single-cell level and distinguishing between the cells by their protein expression profiles. DNA-tagged antibodies provide multiple advantages for profiling proteins in single cells, including the ability to amplify low-abundance tags to make them detectable with sequencing, to use molecular indices for quantitative results, and essentially limitless multiplexing.
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Payam Shahi
10X Genomics (United States)
Samuel Kim
University of California, Irvine
John Haliburton
Chan Zuckerberg Initiative (United States)
Scientific Reports
University of California, San Francisco
QB3
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Shahi et al. (Tue,) studied this question.
synapsesocial.com/papers/6a125972965b75813866d9f8 — DOI: https://doi.org/10.1038/srep44447
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