Construction and application of bispecific antibody EGFR*CD3
A bispecific antibody, antibody technology, applied in the direction of antibodies, anti-animal/human immunoglobulin, anti-receptor/cell surface antigen/cell surface determinant immunoglobulin, etc., can solve the problem of limited efficacy in solid tumors , to increase the effect of immunotherapy and improve the efficacy
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Embodiment 1
[0066] Example 1: Construction of expression vectors for bispecific antibodies (EGFR×CD3, M1001, M1003)
[0067] 1. Bispecific antibody sequence design
[0068] The bispecific antibody targeting EGFR and CD3 is named EGFR×CD3MSBODY, in which the monovalent unit is the anti-EGFR heavy chain and light chain pair, and the amino acid sequence of the variable region refers to the sequence of the monoclonal antibody Erbitux (PDB database sequence number 1YY8 ) and the sequence of Vectibix (the source is the sequence number 38 and 49 in the patent US6235883), including the anti-EGFR heavy chain and light chain, containing Fab and Fc domains; the single-chain unit is the ScFv-Fc form of anti-CD3, the variable region Amino acids refer to the sequence of monoclonal antibody L2K (refer to US20070123479 sequence number 2), including anti-CD3 VH, VL, and Fc domains. Among them, the heavy chain Fc of the monovalent unit and the Fc of the single chain unit (same as the heavy chain Fc of hum...
Embodiment 2
[0100] Example 2: Expression and purification of bispecific antibodies
[0101] 1. Expression of bispecific antibodies
[0102] The endotoxin-free large-scale extraction kit (Qiagen, 12391) was used for large-scale extraction of plasmids, and the specific operation was performed according to the instructions provided by the manufacturer. CHO-S cells were cultured in CD FortiCHO medium (Invitrogen, Cat. 2 The cells were cultured in the incubator. After the cells were prepared, the plasmid pCHO1.0-Erbitux-HL-KKW and pCHO1.0-Hygromycin-L2K-ScFv- Fc-LDY were co-transfected into CHO-S cells to express anti-EGFR×CD3 bispecific antibody M1001; the plasmid pCHO1.0-Vectibix-HL-KKW and pCHO1.0-hygromycin -L2K-ScFv-Fc-LDY were co-transfected into CHO-S cells in the same way as above to express the anti-EGFR×CD3 bispecific antibody M1003. After culturing for 14 days, the expression supernatant was harvested by centrifugation at 800×g.
[0103] 2. Purification of bispecific antibodies ...
Embodiment 3
[0105] Example 3: Determination of the binding activity of bispecific antibodies to cells (FACS)
[0106] The bispecific antibody of the invention binds to the target antigen on the corresponding cell. In the present invention, HT29 (purchased from China Center for Type Culture Collection) is used as EGFR-positive cells, Jurkat (ATCC, TIB-152) is used as CD3-positive cells, and the cell binding activity is determined by the diabody prepared in the present invention.
[0107] 1. Detection of binding activity of bispecific antibody to HT29 cells by flow cytometry
[0108] Sufficient HT29 cells were cultivated, digested with 0.25% trypsin, and collected by centrifugation. Simultaneously dilute the bispecific antibody, starting from 160nM, 4-fold serial dilution to obtain 6 concentration gradients for future use. Wash the collected cells twice with PBS+1%FBS, then resuspend the cells in PBS+1%FBS to 4×10 6 cells / ml, the cells were plated in a 96-well plate, 50ul per well (2×10 ...
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