Haem-dependent dimerization of PGRMC1/Sigma-2 receptor facilitates cancer proliferation and chemoresistance

نویسندگان

  • Yasuaki Kabe
  • Takanori Nakane
  • Ikko Koike
  • Tatsuya Yamamoto
  • Yuki Sugiura
  • Erisa Harada
  • Kenji Sugase
  • Tatsuro Shimamura
  • Mitsuyo Ohmura
  • Kazumi Muraoka
  • Ayumi Yamamoto
  • Takeshi Uchida
  • So Iwata
  • Yuki Yamaguchi
  • Elena Krayukhina
  • Masanori Noda
  • Hiroshi Handa
  • Koichiro Ishimori
  • Susumu Uchiyama
  • Takuya Kobayashi
  • Makoto Suematsu
چکیده

Progesterone-receptor membrane component 1 (PGRMC1/Sigma-2 receptor) is a haem-containing protein that interacts with epidermal growth factor receptor (EGFR) and cytochromes P450 to regulate cancer proliferation and chemoresistance; its structural basis remains unknown. Here crystallographic analyses of the PGRMC1 cytosolic domain at 1.95 Å resolution reveal that it forms a stable dimer through stacking interactions of two protruding haem molecules. The haem iron is five-coordinated by Tyr113, and the open surface of the haem mediates dimerization. Carbon monoxide (CO) interferes with PGRMC1 dimerization by binding to the sixth coordination site of the haem. Haem-mediated PGRMC1 dimerization is required for interactions with EGFR and cytochromes P450, cancer proliferation and chemoresistance against anti-cancer drugs; these events are attenuated by either CO or haem deprivation in cancer cells. This study demonstrates protein dimerization via haem-haem stacking, which has not been seen in eukaryotes, and provides insights into its functional significance in cancer.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2016