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Updated: May 29, 2026
Construction of Synthetic Phage Displayed Fab Library with Tailored Diversity
Published on: May 1, 2018
[Construction of rheumatoid arthritis-specific full-length fully human mammalian display antibody libraries]
Ye Zhou1, Zhen-rui Chen, Wei He
1Institute of Genetic Engineering, Southern Medical University, Guangzhou, China. lzhouye@126.com
Objective:
To construct a rheumatoid arthritis-specific full-length fully human mammalian display antibody libraries.
Methods:
Peripheral blood lymphocytes were isolated from patients with rheumatoid arthritis. The repertoires of kappa light chain (LCκ) and heavy chain variable region (VH) of the antibodies were amplified by RT-PCR. The amplified LCκ and VH genes were inserted into the vector pDGB-HC-TM separately, and the ligated libraries were transformed into competent E.coli TOPO-10 strain to construct the rheumatoid arthritis-specific antibody heavy and light chain libraries. 293T cells were co-transfected with the libraries and the full-length fully human antibody expressed on the surface of 293T cells were analyzed by flow cytometry.
Results:
The libraries of rheumatoid arthritis-specific antibody LCκ and heavy chain (IgG1) were constructed. The expression of full-length fully human antibody on the surface of 293T cells was confirmed by flow cytometry. With the rates of correct LCκ and heavy chain sequence insertion reaching 80% and 60%, respectively, as shown by DNA sequence analysis of the randomly selected clones, the libraries showed an expressible combinatory diversity of 6.13×10(10).
Conclusion:
The constructed libraries provide a useful platform for screening rheumatoid arthritis-specific antibodies.
