PHAGE DISPLAY USED FOR GENE CLONING OF HUMAN RECOMBINANT ANTIBODY AGAINST THE ERYTHROCYTE SURFACE-ANTIGEN, RHESUS-D

被引：36

作者：

DZIEGIEL, M

NIELSEN, LK

ANDERSEN, PS

BLANCHER, A

DICKMEISS, E

ENGBERG, J

机构：

[1] ROYAL DANISH SCH PHARM,DEPT BIOL,DK-2100 COPENHAGEN,DENMARK

[2] CHU PURPAN,CTR REG TRANSFUS SANGUINE TOULOUSE,F-31052 TOULOUSE,FRANCE

来源：

JOURNAL OF IMMUNOLOGICAL METHODS | 1995年 / 182卷 / 01期

关键词：

PHAGE DISPLAY; RHESUS D; AGGLUTINATION; RECOMBINANT ANTIBODY; ERYTHROCYTE;

D O I：

10.1016/0022-1759(95)00013-Z

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

A novel phage display system has been developed for PCR amplification and cloning of the Fab fragments of human immunoglobulin genes. Using this system, we have cloned an antibody from a mouse-human hybridoma cell line directed against the erythrocyte antigen rhesus D. Intact erythrocytes were used for absorption of the Fab phages. Soluble Fab fragments produced from the cloned material showed identical performance to the parental antibody in agglutination assays. Gel filtration confirmed that the Fab fragment consists of a kappa-Fd heterodimer. The successful use of intact cells for selection of specific Fab phages demonstrates that it is possible to by-pass purification of the antigen of interest. Comparison with published germline sequences demonstrated that the immunoglobulin coding regions had the highest homology to the V-H 1.9III and V, Hum kappa v325 germline genes, respectively.

引用

页码：7 / 19

页数：13

共 26 条

[1] EFFICIENT SECRETION OF MURINE FAB FRAGMENTS BY ESCHERICHIA-COLI IS DETERMINED BY THE 1ST CONSTANT DOMAIN OF THE HEAVY-CHAIN [J].