VEGF (Vascular Endothelial Growth Factor) resistant antibody and application thereof
A technology of human antibody and variable region, which is applied in the field of biotechnology and immunology to achieve the effects of growth inhibition, strong antibody antigen binding ability, and inhibition of proliferation of vascular endothelial cells
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Embodiment 1
[0029] Example 1 Antibody Screening
[0030] In order to avoid the bias of individual immune background and ensure the diversity of the antibody library as much as possible, the peripheral blood of 162 healthy adults and 10 neonatal umbilical cord blood lymphocytes were separated by lymphocyte separation medium, and a total of 2×10 lymphocytes were collected. 9 cells. Total RNA was extracted by Trizol method, reverse transcribed into cDNA, and the variable region genes of different antibody subtypes were amplified by conventional PCR. According to the pDF information of the antibody library vector, the restriction site BssH II, Nhe I and the connecting peptide with the Loxp511 sequence were introduced, and then spliced into ScFv (single-chain antibody: VL-Linker (containing the Loxp511 sequence)-VH, above) by overlapping PCR method BssH II and Nhe I sites) were introduced downstream respectively (for specific methods, see "Biological Library Technology", edited by Shao Ning...
Embodiment 2
[0033] Example 2 Antibody expression and purification
[0034] The obtained 4D3 clone variable region gene was cloned into the eukaryotic expression vector containing the human IgG constant region gene to construct the whole antibody expression vector pCMV-163, its physical map is as follows figure 1 shown. The whole antibody is called FD006 antibody. The obtained eukaryotic expression vector was transfected into CHO cells by liposome-mediated method, and ELISA test (using goat anti-human IgG and horseradish enzyme-labeled goat anti-human IgG to perform double-sandwich ELISA method to detect the supernatant Antibody content (with non-transfected supernatant as negative control and pure human IgG as standard), detect antibody expression in culture supernatant, and screen to obtain monoclonal cell lines with higher expression.
[0035] The results of ELISA experiments showed that the antibody was expressed in the expression supernatant, and the expression level was about 15.3±...
Embodiment 3
[0036] Example 3 Antibody Affinity Determination
[0037] Antibody association and dissociation constants were determined using Fortibio.
[0038] Using Octet RED (Fortebio, USA) instrument, the affinity of anti-VEGF antibody was determined. Antibody concentration diluted in PBS was 10 μg / mL, coated with AHC sensor; PBS was used as control, diluted VEGF concentration was 1 μg / mL, 3 μg / mL, 10 μg / mL, and the binding and dissociation curves of the interaction between anti-VEGF antibody and VEGF were determined; Globe Fitting fits the curve and calculates the binding constant, dissociation constant and affinity constant of the interaction between the two. The results are shown in Table 1, the FD006 antibody affinity is 3.11×10 -10 , slightly higher than Avastin's 6.50×10 -10 .
[0039] Table 1. Affinity analysis of the interaction between Avastin antibody and FD006 antibody and VEGF
[0040]
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