Research ArticleStress responses

The endoplasmic reticulum–residing chaperone BiP is short-lived and metabolized through N-terminal arginylation

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Sci. Signal.  02 Jan 2018:
Vol. 11, Issue 511, eaan0630
DOI: 10.1126/scisignal.aan0630

Article Information

vol. 11 no. 511

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History: 
  • Received February 27, 2017
  • Accepted November 28, 2017

Author Information

  1. Sang Mi Shim1,2,
  2. Ha Rim Choi1,2,
  3. Ki Woon Sung1,2,
  4. Yoon Jee Lee1,2,
  5. Sung Tae Kim1,2,3,
  6. Daeho Kim1,4,
  7. Su Ran Mun1,2,
  8. Joonsung Hwang5,
  9. Hyunjoo Cha-Molstad5,
  10. Aaron Ciechanover1,6,
  11. Bo Yeon Kim5,*, and
  12. Yong Tae Kwon1,2,7,*
  1. 1Protein Metabolism Medical Research Center, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  2. 2Department of Biomedical Sciences, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  3. 3Center for Pharmacogenetics and Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  4. 4Department of Biophysics and Chemical Biology, College of Natural Sciences, Seoul National University, Seoul 08826, Republic of Korea.
  5. 5World Class Institute, Korea Research Institute of Bioscience and Biotechnology, Ochang, Cheongwon 28116, Republic of Korea.
  6. 6Tumor and Vascular Biology Research Center, Rappaport Faculty of Medicine and Research Institute, Technion–Israel Institute of Technology, Haifa 31096, Israel.
  7. 7Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  1. *Corresponding author. Email: yok5{at}snu.ac.kr (Y.T.K.); bykim{at}kribb.re.kr (B.Y.K.)

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