Purification of full-length human Pregnane and Xenobiotic Receptor:polyclonal antibody preparation for immunological characterization  

作　　者：Mallampati SARADHI Biji KRISHNA Gauranga MUKHOPADHYAY Rakesh K TYAGI 

机构地区：[1]Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi 110067, India,Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi 110067, India,Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi 110067, India,Special Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi 110067, India

出　　处：《Cell Research》2005年第10期785-795,共11页细胞研究（英文版）

摘　　要：Pregnane and Xenobiotic Receptor (PXR; or Steroid and Xenobiotic Receptor, SXR), a new member of the nuclear receptor superfamily, is thought to modulate a network of genes that are involved in xenobiotic metabolism and elimination. To further explore the role of PXR in body’s homeostatic mechanisms, we for the first time, report successful prokary- otic expression and purification of full-length PXR and preparation of polyclonal antibody against the whole protein. The full-length cDNA encoding a 434 amino acids protein was sub-cloned into prokaryotic expression vector, pET-30b and transformed into E. coli BL21(DE3) cells for efficient over expression. The inclusion body fraction, containing the expressed recombinant protein, was purified first by solubilizing in sarcosine extraction buffer and then by affinity column chromatography using Ni-NTA His-Bind matrix. The efficacy of anti-PXR antibody was confirmed by immunocytology, Western blot analysis, EMSA and immunohistochemistry. The antibody obtained was capable of detecting human and mouse PXR with high specificity and sensitivity. Immunofluorescence staining of COS-1 cells transfected with human or mouse PXR showed a clear nuclear localization. Results from immunohistochemistry showed that level of PXR in liver sections is immunologically detectable in the nuclei. Similar to exogenously transfected PXR, Western blot analysis of cell extract from HepG2 and COLO320DM cells revealed a major protein band for endogenous PXR having the expected molecular weight of 50 kDa. Relevance of other immunodetectable bands with reference to PXR isoforms and current testimony are evaluated. Advantages of antibody raised against full-length PXR protein for functional characterization of receptor is discussed and its application for clinical purposes is envisaged.

关 键 词：Pregnane and Xenobiotic Receptor Steroid and Xenobiotic Receptor prokaryotic expression polyclonal antibody isoforms. 

分 类 号：R392.1[医药卫生—免疫学]