Trivalent bispecific antibody and its preparation process and use
A bispecific antibody and antibody technology, applied in the direction of antibodies, chemical instruments and methods, specific peptides, etc., can solve the problems of poor guiding effect and low affinity of target molecules, and achieve the effects of reducing concentration, enhancing effector function, and high affinity
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Embodiment 1
[0053] Example 1 Preparation of anti-Her2 / neu×anti-CD16 trivalent BsAb
[0054] 1. Materials
[0055] Mouse anti-human CD16 monoclonal antibody light chain, heavy chain variable region genes (VL, VH) were cloned from hybridoma cell B88-9, commercially available (refer to "Molecular Cloning" (Science Press, second edition) for experimental methods); mouse anti-P185 erbB2 Monoclonal antibody VL and VH genes were cloned from hybridoma cells Her2 (commercially available), and scFv was synthesized according to conventional methods, and the amino acid sequence of the linking peptide between VL and VH was (GGGGS) 3 (See "Genetic Engineering Antibodies", edited by Dong Zhiwei and Wang Yan); human IgG1 heavy chain first constant region CH1 and kappa chain constant region CL genes were provided by Dr. Yigang Tong of the Academy of Military Medical Sciences (GenBank AF027159, X95747); Escherichia coli strain JM109, BL21(DE3), prokaryotic expression vector pET22b(+) is the standard stra...
Embodiment 2
[0071] Example 2 FACS analysis to detect the activity detection of anti-Her2 / neu×anti-CD16 trivalent BsAb
[0072] 1. Materials
[0073] Same as embodiment one.
[0074] 2. Methods and results
[0075] 1. FACS analysis of the binding activity of BsAb to SK-BR-3 cells
[0076] SK-BR-3 cells were digested with 0.02% EDTA and washed with cold PBA (PBS, 2% BSA, 0.1% NaN 3 ) and washed twice by centrifugation; incubated with BsAb (0.1 mg / L) at 0°C for 30 minutes; washed by cold PBA twice, and incubated with FITC-GAH by shaken at 0°C for 30 minutes; washed twice by cold PBA, and resuspended cells in PBS , analyzed with a Becton-Dickenson FACsort instrument. The results showed that the BsAb could specifically bind to intact SK-BR-3 cells, and the relative average fluorescence intensity was 92.08, which was 25.4 times that of the negative control, as shown in FIG. 12 .
[0077] 2. FACS analysis of the binding activity between BsAb and CD16 surface antigen-positive cells was taken...
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