SCoPE-MS: mass spectrometry of single mammalian cells quantifies proteome heterogeneity during cell differentiation

被引:540
作者
Budnik, Bogdan [1 ]
Levy, Ezra [2 ]
Harmange, Guillaume [2 ]
Slavov, Nikolai [2 ,3 ]
机构
[1] Harvard Univ, Div Sci, MSPRL, FAS, Cambridge, MA 02138 USA
[2] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[3] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
RIBOSOMAL-PROTEINS; STEM-CELLS; DATABASE; DRUG; IDENTIFICATION; CYTOMETRY; PLATFORM; CANCER; RANGE; YEAST;
D O I
10.1186/s13059-018-1547-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Some exciting biological questions require quantifying thousands of proteins in single cells. To achieve this goal, we develop Single Cell ProtEomics by Mass Spectrometry (SCoPE-MS) and validate its ability to identify distinct human cancer cell types based on their proteomes. We use SCoPE-MS to quantify over a thousand proteins in differentiating mouse embryonic stem cells. The single-cell proteomes enable us to deconstruct cell populations and infer protein abundance relationships. Comparison between single-cell proteomes and transcriptomes indicates coordinated mRNA and protein covariation, yet many genes exhibit functionally concerted and distinct regulatory patterns at the mRNA and the protein level.
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页数:12
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