Multiplexed, targeted profiling of single-cell proteomes and transcriptomes in a single reaction

Alex S. Genshaft(Massachusetts Institute of Technology), Shuqiang Li(Broad Institute), Caroline J. Gallant(Uppsala University), Spyros Darmanis(Uppsala University), Sanjay M. Prakadan(Broad Institute), Carly G.K. Ziegler(Massachusetts Institute of Technology), Martin Lundberg(Olink Bioscience (Sweden)), Simon Fredriksson(Olink Bioscience (Sweden)), Joyce Hong(Massachusetts Institute of Technology), Aviv Regev(Massachusetts Institute of Technology), Kenneth J. Livak, Ulf Landegren(Science for Life Laboratory), Alex K. Shalek(Ragon Institute of MGH, MIT and Harvard)
Genome biology
September 19, 2016
Cited by 177Open Access
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Abstract

We present a scalable, integrated strategy for coupled protein and RNA detection from single cells. Our approach leverages the DNA polymerase activity of reverse transcriptase to simultaneously perform proximity extension assays and complementary DNA synthesis in the same reaction. Using the Fluidigm C1™ system, we profile the transcriptomic and proteomic response of a human breast adenocarcinoma cell line to a chemical perturbation, benchmarking against in situ hybridizations and immunofluorescence staining, as well as recombinant proteins, ERCC Spike-Ins, and population lysate dilutions. Through supervised and unsupervised analyses, we demonstrate synergies enabled by simultaneous measurement of single-cell protein and RNA abundances. Collectively, our generalizable approach highlights the potential for molecular metadata to inform highly-multiplexed single-cell analyses.


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