Exp Mol Med.  2008 Apr;40(2):254-260. 10.3858/emm.2008.40.2.254.

An NH(2)-terminal truncated cytochrome P450 CYP3A4 showing catalytic activity is present in the cytoplasm of human liver cells

  • 1Department of Dermatology, Dongguk University School of Medicine,Goyang 410-773, Korea. leeay@duih.org
  • 2Research Institute of Biotechnology, Medical Science Research Center, Dongguk University, Goyang 410-773, Korea.
  • 3School of Biological Sciences and Technology, Chonnam National University, Gwangju 500-757, Korea.
  • 4Department of General Surgery, Eulji University School of Medicine, Seoul 139-872, Korea.
  • 5Department of Internal Medicine, Bundang Hospital, Seoul National University College of Medicine, Seongnam 463-707, Korea.
  • 6Department of General Surgery, Bundang Hospital, Seoul National University College of Medicine, Seongnam 463-707, Korea.
  • 7Department of Internal Medicine, Dongguk University School of Medicine, Goyang 410-773, Korea.


Cytochrome P450 3A4 (CYP3A4), is the dominant human liver hemoprotein enzyme localized in the endoplasmic reticulum (ER), and is responsible for the metabolism of more than 50% of clinically relevant drugs. While we were studying CYP3A4 expression and activity in human liver, we found that anti-CYP3A4 antibody cross-reacted with a lower band in liver cytoplasmic fraction. We assessed the activities of CYP3A4 and its truncated form in the microsomal and cytoplasmic fraction, respectively. In the cytoplasmic fraction, truncated CYP3A4 showed catalytic activity when reconstituted with NADPH-cytochrome P-450 reductase and cytochrome b5. In order to determine which site was deleted in the truncated form in vitro, we transfected cells with N-terminal tagged or C-terminal tagged human CYP3A4 cDNA. The truncated CYP3A4 is the N-terminal deleted form and was present in the soluble cytoplasmic fraction. Our result shows, for the first time, that N-terminal truncated, catalytically active CYP3A4 is present principally in the cytoplasm of human liver cells.


cytochrome P-450 CYP3A; cytoplasm; enzymology; microsomes, liver
Full Text Links
  • EMM
export Copy
  • Twitter
  • Facebook
Similar articles
Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr