Turner T N, Smith C L, Bohach G A
Department of Bacteriology and Biochemistry, University of Idaho, Moscow 83843.
Infect Immun. 1992 Feb;60(2):694-7. doi: 10.1128/iai.60.2.694-697.1992.
Nonconserved residues of staphylococcal enterotoxin C1 (SEC1) were converted to their counterparts in SEC2. The mutants that resulted were examined for reactivity with monoclonal antibodies (MAbs). Substitution at position 20, 22, or 26 interfered with binding of an SEC1-specific MAb. SEC1 mutants with substitutions at all three positions reacted only with an SEC2-specific MAb. Antibody-binding patterns were not associated with isoelectric point differences. All mutants retained biological activity.
将葡萄球菌肠毒素C1(SEC1)的非保守残基替换为SEC2中的对应残基。对所得突变体进行单克隆抗体(MAb)反应性检测。在第20、22或26位的替换干扰了SEC1特异性单克隆抗体的结合。在所有这三个位置都有替换的SEC1突变体仅与SEC2特异性单克隆抗体反应。抗体结合模式与等电点差异无关。所有突变体均保留生物活性。