Single-cell Proteomics: Progress and Prospects

被引:241
作者
Kelly, Ryan T. [1 ]
机构
[1] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
基金
美国国家卫生研究院;
关键词
ELECTROPHORESIS-MASS SPECTROMETRY; SUBAMBIENT PRESSURE IONIZATION; ELECTROSPRAY-IONIZATION; BOTTOM-UP; INTERFACE; MS; SENSITIVITY; EFFICIENCY; COVERAGE; PLATFORM;
D O I
10.1074/mcp.R120.002234
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
MS-based proteome profiling has become increasingly comprehensive and quantitative, yet a persistent short-coming has been the relatively large samples required to achieve an in-depth measurement. Such bulk samples, typically comprising thousands of cells or more, provide a population average and obscure important cellular heterogeneity. Single-cell proteomics capabilities have the potential to transform biomedical research and enable understanding of biological systems with a new level of granularity. Recent advances in sample processing, separations and MS instrumentation now make it possible to quantify >1000 proteins from individual mammalian cells, a level of coverage that required an input of thousands of cells just a few years ago. This review discusses important factors and parameters that should be optimized across the workflow for single-cell and other low-input measurements. It also highlights recent developments that have advanced the field and opportunities for further development.
引用
收藏
页码:1739 / 1748
页数:10
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