Epitope identification for human neutrophil flavocytochrome b monoclonals 48 and 449

被引:19
作者
Burritt, JB
Fritel, GN
Dahan, I
Pick, E
Roos, D
Jesaitis, AJ
机构
[1] Montana State Univ, Dept Microbiol, Bozeman, MT 59717 USA
[2] Tel Aviv Univ, Sackler Sch Med, Dept Human Microbiol, Julius Friedrich Cohnheim Minerva Ctr Phagocyte, IL-69978 Tel Aviv, Israel
[3] Univ Amsterdam, Acad Med Ctr, Cent Lab, Netherlands Blood Transfus Serv, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Expt & Clin Immunol Lab, NL-1105 AZ Amsterdam, Netherlands
关键词
neutrophil; flavocytochrome b; phage display; epitope mapping; monoclonal antibodies;
D O I
10.1034/j.1600-0609.2000.065006407.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Flavocytochrome b(558) (CYt b) is important in generating superoxide and other toxic oxygen species involved in inflammation and host defense. Monoclonal antibodies (mAbs) 48 and 449 bind the gp91(phox) and p22(phox) subunits of Cyt b, respectively, and have been used to characterize this enzyme complex. Until now, data were unavailable to predict which regions of the protein were bound by each antibody. Random sequence phage-display peptide library analysis of each antibody was used to select peptides that mimic the sequence of each protein epitope. Phage sequences selected by mAb 48 presented the consensus peptide sequence DRDVXTGL, which closely resembles (498)EKDVITGL(505) Of gp91(phox). Phage selected by mAb 449 contributed the consensus WRWPGPQVL, resembling in part (182)GpQV(185) Of p22(phox). Confirmation for this second epitope was provided by peptide walking analysis. Identifying the protein residues bound by these antibodies makes each a more informative probe for Cyt b analysis.
引用
收藏
页码:407 / 413
页数:7
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