| Literature DB >> 34524823 |
Stephanie Biedka1, Brigitte F Schmidt2,3, Nolan M Frey3, Sarah M Boothman3, Jonathan S Minden1,3, Amber Lee Wilson1.
Abstract
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.Entities:
Keywords: click chemistry; protein; protein chemistry; protein mass spectrometry; protein modification; proteomics; reversible chemistry; sample cleanup; sample preparation; two-dimensional gel electrophoresis
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Year: 2021 PMID: 34524823 PMCID: PMC9392872 DOI: 10.1021/acs.jproteome.1c00443
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 5.370