論文

査読有り 国際誌
2020年10月20日

PIM 3 kinase, a proto-oncogene product, regulates phosphorylation of the measles virus nucleoprotein tail domain at Ser 479 and Ser 510.

Biochemical and biophysical research communications
  • Akihiro Sugai
  • ,
  • Hiroki Sato
  • ,
  • Misako Yoneda
  • ,
  • Chieko Kai

531
3
開始ページ
267
終了ページ
274
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrc.2020.06.002

The tail domain of the measles virus (MeV) N protein is typically phosphorylated at S479 and S510. However, the protein kinase responsible for this phosphorylation has not been identified. To identify the protein kinase responsible, we conducted an in vitro kinase assay in the presence of various protein kinase inhibitors. Phosphorylation of S479 and S510 was suppressed in the presence of SP600125. We demonstrated that purified PIM 3 kinase, which is sensitive to SP600125, successfully phosphorylated both phosphorylation sites. Inhibitors of PIM kinase, CX6258 and LY294002, also suppressed phosphorylation of the N protein. These findings indicate that PIM 3 kinase is associated with the tail domain of the N protein and that PIM 3 kinase regulates N protein phosphorylation.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2020.06.002
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32800554
ID情報
  • DOI : 10.1016/j.bbrc.2020.06.002
  • PubMed ID : 32800554

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