Construction and application of bispecific antibody HER2*CD3
A bispecific antibody and antibody technology, applied in the direction of antibody, anti-animal/human immunoglobulin, anti-receptor/cell surface antigen/cell surface determinant immunoglobulin, etc., can solve the problem of limited curative effect of solid tumors , to increase the effect of immunotherapy
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Embodiment 1
[0076] Example 1: Construction of expression vectors for bispecific antibodies (HER2×CD3, M802)
[0077] 1. Bispecific antibody sequence design
[0078] The bispecific antibody targeting HER2 and CD3 is named HER2×CD3 MSBODY, in which the monovalent unit is the pair of heavy and light chains against HER2, and the amino acid sequence of the variable region refers to the sequence of the monoclonal antibody Herceptin (PDB database No. .1N8Z), including anti-HER2 heavy chain and light chain, containing Fab and Fc domains; the single chain unit is in the form of anti-CD3 ScFv-Fc, and the amino acids of the variable region refer to the sequence of monoclonal antibody L2K (refer to US20070123479 sequence number 2) , including anti-CD3 VH, VL, 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 human IgG1) are modified by amino acid mutations. For the specific Fc modification process, see PCT / CN2012 / 0849...
Embodiment 2
[0102] Example 2: Expression and purification of bispecific antibodies
[0103] 1. Expression of bispecific antibodies
[0104] 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 CDFortiCHO medium (Invitrogen, Cat. 2 Culture in a cell culture incubator. After the cells were prepared, the plasmid pCHO1.0-Herceptin-HL-KKW and pCHO1.0-Hygromycin-L2K-ScFv were transferred using a MaxcyteSTX electroporator according to the manufacturer's instructions (Maxcyte). -Fc-LDY were co-transfected into CHO-S cells to express the anti-HER2×CD3 bispecific antibody M802. After culturing for 14 days, the expression supernatant was harvested by centrifugation at 800×g.
[0105] 2. Purification of bispecific antibodies
[0106] The expression supernatant was filtered with a 0.22uM filter membrane, and all ...
Embodiment 3
[0107] Example 3: Determination of the binding activity of bispecific antibodies to cells (FACS)
[0108] The bispecific antibody of the invention binds to the target antigen on the corresponding cell. The present invention uses SK-BR-3 (purchased from China Type Culture Collection Center) as HER2-positive cells, Jurkat (American Type Culture Collection (ATCC), TIB-152) as CD3-positive cells, and uses this The diabodies prepared by the invention were tested for their cell binding activity.
[0109] 1. Detection of binding activity of bispecific antibody to SK-BR-3 cells by flow cytometry
[0110] Cultivate enough SK-BR-3 cells, digest with 0.25% trypsin, and collect the cells by centrifugation. Dilute the bispecific antibody at the same time, the concentration starts from 160nmol, and 4-fold gradient dilution is obtained to obtain 6 concentration gradients, which are ready for use. Wash the collected cells twice with PBS+1%FBS, then resuspend the cells in PBS+1%FBS to 4×10 ...
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