Developing Cell-Specific Antibodies to Endothelial Progenitor Cells Using Avian Immune Phage Display Technology

被引:9
|
作者
Bowes, Tyrone [1 ]
Hanley, Shirley A. [1 ]
Liew, Aaron [1 ]
Eglon, Marc [1 ]
Mashayekhi, Kaveh [1 ]
O'Kennedy, Richard [2 ,3 ]
Barry, Frank [1 ]
Taylor, W. Robert [5 ,6 ]
O'Brien, Timothy [1 ]
Griffin, Matthew D. [1 ]
Finlay, William J. J. [2 ,3 ,4 ]
Greiser, Udo [1 ]
机构
[1] Natl Univ Ireland, Regenerat Med Inst, Natl Ctr Biomed Engn Sci, Galway, Ireland
[2] Dublin City Univ, Sch Biotechnol, Dublin 9, Ireland
[3] Dublin City Univ, Biomed Diagnost Inst, Dublin 9, Ireland
[4] Pfizer R&D, Dublin, Ireland
[5] Emory Univ, Sch Med, Dept Med & Biomed Engn, Atlanta, GA USA
[6] Atlanta VA Med Ctr, Atlanta, GA USA
基金
爱尔兰科学基金会;
关键词
phage display; single-chain antibodies; endothelial progenitor cells; cell surface markers; vasculature; CORONARY-ARTERY-DISEASE; MONOCLONAL-ANTIBODY; PERIPHERAL-BLOOD; CHICKEN GENOME; FRAGMENTS; GENERATION; ANGIOGENESIS; PHENOTYPE; LIBRARIES; SYSTEM;
D O I
10.1177/1087057111407067
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This study aims at generating immune chicken phage display libraries and single-chain antibodies (scFvs) specifically directed against cell surface markers of cultured peripheral blood mononuclear cells (PBMCs) that contain endothelial progenitor cells (EPCs). In contrast to previous approaches that use well-defined recombinant antigens attached to plastic surfaces that may alter the structure of the proteins, the authors describe a method that maintains the cell surface markers on live cells while providing the opportunity to rapidly screen entire libraries for antibodies that bind to unknown cell surface markers of progenitor/stem cells. Chickens immunized with live EPCs, consisting of a heterogeneous population of lymphocytes and monocytes, demonstrated a robust immune response. After three rounds of biopanning, the authors purified and characterized three unique scFvs called UG1-3. Codon-optimized recombinant UG1 (gUG-1) shows binding by flow cytometry to circulating CD14-positive cells in peripheral blood consistent with predominant expression of a target protein on monocyte subsets. The authors describe the successful use of immunization of chickens for the generation of scFvs against a heterogenous population of EPCs displaying unknown cell surface markers and demonstrate the strong potential of phage display technology in the development of reagents for the isolation and characterization of stem/progenitor cells. (Journal of Biomolecular Screening. 2011; 16: 744-754)
引用
收藏
页码:744 / 754
页数:11
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