Sloan D D, Barrett R W, Tate E H, England B P
Affymax Research Institute, Palo Alto, California 94304, USA.
Protein Expr Purif. 1997 Oct;11(1):119-24. doi: 10.1006/prep.1997.0777.
In order to screen combinatorial libraries of peptides and/or small organic molecules against the human C5a receptor, we have developed a novel method for immobilizing and screening 7-transmembrane segment (7-TMS) receptors. The epitope for a high affinity monoclonal antibody (mAb179) was added to the C-terminus of the human C5a receptor, and CHO cell lines expressing the epitope tagged receptor (C5aR-KH) and the wild-type receptor (C5aR) were established. The addition of the epitope tag did not affect the affinity of C5aR-KH for C5a. The epitope tag allowed for mAb179-mediated immobilization of active receptor either in intact membranes or following detergent extraction with digitonin or Chaps. If this method is generally applicable to other 7-TMS receptors it may have broad utility for drug discovery screening as well as other applications.
为了筛选针对人C5a受体的肽和/或小有机分子组合文库,我们开发了一种用于固定和筛选7跨膜结构域(7-TMS)受体的新方法。将高亲和力单克隆抗体(mAb179)的表位添加到人C5a受体的C末端,并建立了表达表位标记受体(C5aR-KH)和野生型受体(C5aR)的CHO细胞系。表位标签的添加不影响C5aR-KH对C5a的亲和力。该表位标签允许mAb179介导的活性受体在完整膜中或在用洋地黄皂苷或CHAPS进行去污剂提取后固定。如果该方法普遍适用于其他7-TMS受体,它可能在药物发现筛选以及其他应用中具有广泛的用途。