| Literature DB >> 28105180 |
Fei Liu1, Chun-Ling Qi2, Mian Kong3, Ting-Ting Liu1, Lei Li1, Bao-Jiang Li1.
Abstract
The present study aimed to identify polypeptides that specifically bond to breast cancer stem cells from a phage display random 12 peptide library, in addition to the affinity and specificity of polypeptides. A phage display random 12 peptide library was screened using breast cancer stem cells as targets isolated from the MDA-MB-231 cell line using the serum-free culture technique with hs578bst and MDA-MB-231 cells as subtract-screening cells. Positive and specific binding clones were amplified and sent for sequencing. The affinity and specificity of the positive clones were subsequently identified by ELISA and 3,3'-diaminobenzidine staining. The results demonstrated that phages were gathered ~500 times following three rounds of biopanning. ELISA identified that the affinity to breast cancer stem cells of the no. 6 phage was 6.14 times higher than that in the control group. In addition, immunohistochemistry observed that the no. 6 phage exhibited high-specificity bonding to breast cancer stem cells, and the peptide sequence of the positive phage was GYSASRSTIPGK following DNA sequencing and translation. Thus, the present study isolated a specific peptide that bonds to breast cancer stem cells from a phage display random peptide library, which may facilitate further studies regarding the stem cell-targeted therapy of breast cancer.Entities:
Keywords: breast cancer stem cell; phage display random 12 peptide library; polypeptide; subtract screening
Year: 2016 PMID: 28105180 PMCID: PMC5228583 DOI: 10.3892/ol.2016.5248
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967