4.5 Article

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

Journal

CELL CHEMICAL BIOLOGY
Volume 25, Issue 11, Pages 1380-+

Publisher

CELL PRESS
DOI: 10.1016/j.chembiol.2018.08.006

Keywords

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Funding

  1. National Natural Science Foundation of China [31671428, 31500665, 31530041]
  2. National Key R&D Program of China [2016YFA0501900, 2016YFA0501904]
  3. 100 Talents Program of the Chinese Academy of Sciences

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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 stressregulated selenoproteomes for nine tissues from mice of different ages and mammalian cells, demonstrating tissue-specific selenoproteomes and an age-dependent decline in specific selenoproteins in brains and hearts. We established an integrated platform using SecMS and SECIS-independent selenoprotein (SIS) database and further identified five candidate selenoproteins. The application of this integrated platform provides an effective strategy to explore the selenoproteome independent of SECIS.

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