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Selenocysteine-Specific Mass Spectrometry Reveals Tissue-Distinct Selenoproteomes and Candidate Selenoproteins.

Cell Chem Biol. 2018; 
Guo L, Yang W, Huang Q, Qiang J, Hart JR, Wang W, Hu J, Zhu J, Liu N, Zhang Y.
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Recombinant Proteins 02444 Isopropanol Sigma-Aldrich Cat#W292907 Tris (hydroxymethyl) aminomethane (Tris) Sigma-Aldrich Cat#T5941 Dithiothreitol (DTT) Sigma-Aldrich Cat#43815 Citric acid Sigma-Aldrich Cat#C2404 Trypsin Promega Cat#V511A Protease inhibitor cocktail Sigma-Aldrich Cat#11836145001 QVNEDELUQK GenScript N/A LAEEHGSUGTPAK GenScript N/A MAUASSVEWR FUSSLDFR (labeled Get A Quote

Abstract

Selenoproteins, defined by the presence of selenocysteines (Sec), play important roles in a wide range of biological processes. All known selenoproteins are marked by the presence of Sec insertion sequence (SECIS) at their mRNA. The lack of an effective analytical method has hindered our ability to explore the selenoproteome and new selenoproteins beyond SECIS. Here, we develop a Sec-specific mass spectrometry-based technique, termed "SecMS," which allows the systematic profiling of selenoproteomes by selective alkylation of Sec. Using SecMS, we quantitatively characterized the age- and stress-regulated selenoproteomes for nine tissues from mice of different ages and mammalian cells, demonstrating tissue-specif... More

Keywords

Sec-specific mass spectrometry (SecMS); alkylation; quantitative proteomics; selenocysteine; selenoprotein; selenoproteomes