Preparation and activity detection of monoclonal antibody against anti-CD3 ScFv.
- Author:
Xiao-Feng SHAO
1
;
Ying-Dai GAO
;
Juan-Ni LIU
;
Jin-Hong WANG
;
Yuan-Fu XU
;
Dong-Mei FAN
;
Chun-Zheng YANG
;
Dong-Sheng XIONG
Author Information
- Publication Type:Journal Article
- MeSH: Antibodies, Monoclonal; biosynthesis; immunology; isolation & purification; CD3 Complex; immunology; Cell Line; Chromatography, Affinity; Humans; Hybridomas; metabolism; Jurkat Cells; K562 Cells
- From: Acta Academiae Medicinae Sinicae 2008;30(3):354-359
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo prepare monoclonal antibody (McAb) against anti-CD3 ScFv for purifying and detecting serum anti-CD3 antibody concentration.
METHODSMcAb against anti-CD3 ScFv was prepared by hybridoma technique and used to prepare affinity chromatography column, which was used to purify anti-CD3 ScFv and Diabody [CD3 x Pgp] without E-tag. The binding activities of anti-CD3 ScFv, Diabody [CD3 x Pgp] without E-tag, and Diabody [CD3 x Pgp] purified by anti-CD3 affinity chromatography column or anti-E-tag affinity chromatography column against K562/A02 cell and Jurket cells were detected by fluorescence activated cell sorting (FACS) method. ELISA was used to identify the specificity of the McAb.
RESULTSMcAb against anti-CD3 ScFv specifically detected serum anti-CD3 ScFv without reacting with sera. The anti-CD3 ScFv purified by anti-CD3 affinity chromatography column and purified by anti-E-tag affinity chromatography column had the same specific binding activity with Jurkat cells. The positive binding rates of Diabody [CD3 x Pgp] without E-tag to K562/A02 and Jurkat cells were 89.87% and 83.95%, respectively. In the competitive binding experiments with K562/A02 and Jurkat cells, the binding rates of Diabody [CD3 x Pgp] without E-tag decreased to 56.30% and 43.78%, respectively.
CONCLUSIONThe McAb against anti-CD3 ScFv prepared in our lab can be used to purify and detect serum anti-CD3 antibody concentration.