Reversible Click Chemistry Tag for Universal Proteome Sample Preparation for Top-Down and Bottom-Up Analysis

被引:5
|
作者
Biedka, Stephanie [1 ]
Schmidt, Brigitte F. [2 ,3 ]
Frey, Nolan M. [3 ]
Boothman, Sarah M. [3 ]
Minden, Jonathan S. [1 ,3 ]
Lucas, Amber [1 ]
机构
[1] Impact Prote LLC, Pittsburgh, PA 15206 USA
[2] JGS Res Co, Pittsburgh, PA 15212 USA
[3] Carnegie Mellon Univ, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
sample preparation; click chemistry; proteomics; protein; protein modification; protein chemistry; sample cleanup; two-dimensional gel electrophoresis; protein mass spectrometry; reversible chemistry; BIOMARKER DISCOVERY; QUANTIFICATION; MIXTURES; STRATEGY;
D O I
10.1021/acs.jproteome.1c00443
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Successful proteome analysis requires reliable sample preparation beginning with protein solubilization and ending with a sample free of contaminants, ready for downstream analysis. Most proteome sample preparation technologies utilize precipitation or filter-based separation, both of which have significant disadvantages. None of the current technologies are able to prepare both intact proteins or digested peptides. Here, we introduce a reversible protein tag, ProMTag, that enables whole proteome capture, cleanup, and release of intact proteins for top-down analysis. Alternatively, the addition of a novel Trypsin derivative to the workflow generates peptides for bottom-up analysis. We show that the ProMTag workflow yields >90% for intact proteins and >85% for proteome digests. For top-down analysis, ProMTag cleanup improves resolution on 2D gels; for bottom-up exploration, this methodology produced reproducible mass spectrometry results, demonstrating that the ProMTag method is a truly universal approach that produces high-quality proteome samples compatible with multiple downstream analytical techniques. Data are available via ProteomeXchange with identifier PXD027799.
引用
收藏
页码:4787 / 4800
页数:14
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