Nieves R A, Himmel M E, Todd R J, Ellis R P
Department of Microbiology, Colorado State University, Fort Collins 80525.
Appl Environ Microbiol. 1990 Apr;56(4):1103-8. doi: 10.1128/aem.56.4.1103-1108.1990.
Splenocytes derived from mice inoculated with a commercial cellulase preparation or purified cellulases were fused with a stable myeloma cell line (SP2/0). Specific monoclonal antibodies to cellobiohydrolases I and II and endoglucanases I and II were established. In addition to specific monoclonal antibodies, we were also able to establish stable hybridoma cell lines which produced monoclonal antibodies that recognized similar epitopes possessed by two or more of the above cellulases. By obtaining monospecific antibodies for all four individual cellulases, the role and function of the individual cellulases can thus be studied in greater detail.
将接种了商业纤维素酶制剂或纯化纤维素酶的小鼠的脾细胞与稳定的骨髓瘤细胞系(SP2/0)进行融合。建立了针对纤维二糖水解酶I和II以及内切葡聚糖酶I和II的特异性单克隆抗体。除了特异性单克隆抗体外,我们还能够建立稳定的杂交瘤细胞系,这些细胞系产生的单克隆抗体能够识别上述两种或更多种纤维素酶所共有的相似表位。通过获得针对所有四种单独纤维素酶的单特异性抗体,从而可以更详细地研究各个纤维素酶的作用和功能。