PURIFICATION OF E-COLI-SYNTHESIZED PAN PROTEINS AND DEVELOPMENT OF A PAN-SPECIFIC MONOCLONAL-ANTIBODY

被引:3
作者
VIERRA, CA
XIN, XQ
JACOBS, YT
CAMPBELL, JM
SHEN, LP
RUTTER, WJ
NELSON, C
机构
[1] UNIV CALIF RIVERSIDE,DEPT BIOCHEM,RIVERSIDE,CA 92521
[2] CHIRON CORP,EMERYVILLE,CA 94608
[3] UNIV CALIF SAN FRANCISCO,HORMONE RES INST,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94143
来源
HYBRIDOMA | 1994年 / 13卷 / 03期
关键词
D O I
10.1089/hyb.1994.13.191
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The helix-loop-helix (HLH) transcription factors, Pan-1 (E47) and Pan-2 (E12), are produced by the mechanism of alternative transcript splicing. Pan-1 and Pan-2 were expressed in Escherichia coli, and a purification scheme was developed. Purified Pan-2 was used to immunize Smith-Webster mice and a hybridoma was generated that produced a monoclonal antibody (Yae) that specifically recognized both native and denatured Pan-1 and Pan-2. Deletion mapping and sequence transfer studies have localized the determinant recognized by the Yae antibody to the region 195-208 of Pan-2, This region is conserved in Pan-1 and Pan-2. The Yae antibody recognized in vitro-synthesized ITF-1, a third E2A (Pan) gene product also produced by the mechanism of alternative RNA splicing, but did not recognize the related HLH proteins, ITF-2, REB alpha, or REB beta. By Western blot assay of pancreatic acinar cells, the Yae antibody detected a single protein species of 72 kD that comigrated with in vitro-synthesized Pan-1 and Pan-2.
引用
收藏
页码:191 / 197
页数:7
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