Selenoprotein S is involved in maintenance and transport of multiprotein complexes

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Turanov A. A., Shchedrina V. A., Everley R. A., Lobanov A. V., Yim S. H., Marino S. M., ...Daha Fazla

BIOCHEMICAL JOURNAL, cilt.462, ss.555-565, 2014 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 462
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1042/bj20140076
  • Dergi Adı: BIOCHEMICAL JOURNAL
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.555-565
  • Anahtar Kelimeler: coiled-coil domain, multiprotein complex, protein-protein interaction, selenocysteine, selenoprotein S, MEMBRANE-PROTEIN, MISFOLDED PROTEINS, SELENIUM, DISLOCATION, EXPRESSION, GENE, RETROTRANSLOCATION, SELENOCYSTEINE, NETWORKS, STRESS
  • Akdeniz Üniversitesi Adresli: Evet

Özet

SelS (Selenoprotein S) is a selenocysteine-containing protein with roles in ER (endoplasmic reticulum) function and inflammation. It has been implicated in ERAD (ER-associated protein degradation), and clinical studies revealed an association of its promoter polymorphism with cytokine levels and human diseases. However, the pathways and interacting proteins that could shed light on pathogenesis of Se1S-associated diseases have not been studied systematically. We performed a large-scale affinity isolation of human SelS and its mutant forms and analysed the proteins that interact with them. All previously known SelS targets and nearly two hundred additional proteins were identified that were remarkably enriched for various multiprotein complexes. Subsequent chemical cross-linking experiments identified the specific interacting sites in SelS and its several targets. Most of these interactions involved coiled-coil domains. The data suggest that SelS participates in intracellular membrane transport and maintenance of protein complexes by anchoring them to the ER membrane.