PLoS ONE (Aug 2009)

Protein-protein interactions of tandem affinity purified protein kinases from rice.

  • Jai S Rohila,
  • Mei Chen,
  • Shuo Chen,
  • Johann Chen,
  • Ronald L Cerny,
  • Christopher Dardick,
  • Patrick Canlas,
  • Hiroaki Fujii,
  • Michael Gribskov,
  • Siddhartha Kanrar,
  • Lucas Knoflicek,
  • Becky Stevenson,
  • Mingtang Xie,
  • Xia Xu,
  • Xianwu Zheng,
  • Jian-Kang Zhu,
  • Pamela Ronald,
  • Michael E Fromm

DOI
https://doi.org/10.1371/journal.pone.0006685
Journal volume & issue
Vol. 4, no. 8
p. e6685

Abstract

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Eighty-eight rice (Oryza sativa) cDNAs encoding rice leaf expressed protein kinases (PKs) were fused to a Tandem Affinity Purification tag (TAP-tag) and expressed in transgenic rice plants. The TAP-tagged PKs and interacting proteins were purified from the T1 progeny of the transgenic rice plants and identified by tandem mass spectrometry. Forty-five TAP-tagged PKs were recovered in this study and thirteen of these were found to interact with other rice proteins with a high probability score. In vivo phosphorylated sites were found for three of the PKs. A comparison of the TAP-tagged data from a combined analysis of 129 TAP-tagged rice protein kinases with a concurrent screen using yeast two hybrid methods identified an evolutionarily new rice protein that interacts with the well conserved cell division cycle 2 (CDC2) protein complex.