NOVEL T-CELL ANTIGEN 4-1BB ASSOCIATES WITH THE PROTEIN-TYROSINE KINASE P56(LCK1)

被引:0
|
作者
KIM, YJ
POLLOK, KE
ZHOU, Z
SHAW, A
BOHLEN, JB
FRASER, M
KWON, BS
机构
[1] INDIANA UNIV,SCH MED,WALTHER ONCOL CTR,DEPT MICROBIOL & IMMUNOL,635 BARNHILL DR,INDIANAPOLIS,IN 46202
[2] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
[3] BRISTOL MYERS SQUIBB,PHARMACEUT RES INST,PRINCETON,NJ 08543
[4] UNIV NOTRE DAME,DEPT BIOL SCI,NOTRE DAME,IN 46556
来源
JOURNAL OF IMMUNOLOGY | 1993年 / 151卷 / 03期
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
4-1BB is a 30-kDa inducible T cell Ag, and is expressed predominantly as a 55-kDa dimer on both CD4+ and CD8+ T lymphocytes. The cytoplasmic tail of 4-1BB contains the sequence Cys-Arg-Cys-Pro, which is similar to the sequence Cys-X-Cys-Pro, which mediates the binding of the CD4 and CD8 molecules to the protein tyrosine kinase p56lck . An anti-4-1BB mAb, 53A2, was used to determine whether 4-1BB may associate with p56lck. The 53A2 mAb specifically recognized 4-1BB on a CD8+ T cell line, CTLL-2, and coimmunoprecipitated a 56-kDa protein along with 4-1 BB. Peptide mapping indicated that the 56-kDa phosphoprotein was identical to p56lck. The coimmunoprecipitation of p56lck with 4-1BB also occurred in nonlymphoid cells such as insect (Sf-21) and HeLa cells when the two recombinant proteins were coexpressed. Analysis of mutant p56lck recombinant proteins showed that two cysteine residues critical for p56lck-D4 (or -CD8) complex formation are also required for the p56lck-4-1BB interaction. These studies establish that 4-1BB physically associates with p56lck. 151: 1255.
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页码:1255 / 1262
页数:8
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