Single-cell Proteomics Preparation for Mass Spectrometry Analysis using Freeze-Heat Lysis and an Isobaric Carrier

被引:6
|
作者
Petelski, Aleksandra A. [1 ]
Slavov, Nikolai [1 ,2 ,3 ]
Specht, Harrison [1 ]
机构
[1] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[2] Northeastern Univ, Barnett Inst, Boston, MA USA
[3] Northeastern Univ, Dept Biol, Boston, MA USA
来源
关键词
D O I
10.3791/63802
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-cell proteomics analysis requires sensitive, quantitatively accurate, widely accessible, and robust methods. To meet these requirements, the Single-Cell ProtEomics (SCoPE2) protocol was developed as a second-generation method for quantifying hundreds to thousands of proteins from limited samples, down to the level of a single cell. Experiments using this method have achieved quantifying over 3,000 proteins across 1,500 single mammalian cells (500-1,000 proteins per cell) in 10 days of mass spectrometer instrument time. SCoPE2 leverages a freeze-heat cycle for cell lysis, obviating the need for clean-up of single cells and consequently reducing sample losses, while expediting sample preparation and simplifying its automation. Additionally, the method uses an isobaric carrier, which aids protein identification and reduces sample losses.This video protocol provides detailed guidance to enable the adoption of automated single-cell protein analysis using only equipment and reagents that are widely accessible. We demonstrate critical steps in the procedure of preparing single cells for proteomic analysis, from harvesting up to injection to liquid chromatography -tandem mass spectrometry (LC-MS/MS) analysis. Additionally, viewers are guided through the principles of experimental design with the isobaric carrier, quality control for both isobaric carrier and single-cell preparations, and representative results with a discussion of limitations of the approach.
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页数:14
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