Lewis D M, Lewis J C, Loegering D A, Gleich G J
J Cell Biol. 1978 Jun;77(3):702-13. doi: 10.1083/jcb.77.3.702.
The localization of the guinea pig eosinophil major basic protein (MBP) within the cell was investigated by the use of immunoelectron microscopy and by isolation of the granule crystalloids. First, by immunoperoxidase electron microscopy, we found that the MBP of eosinophil granules is contained within the crystalloid core of the granule. Specific staining of cores was present when rabbit antiserum to MBP was used as the first stage antibody in a double antibody staining procedure, whereas staining was not seen when normal rabbit serum was used as the first stage antibody. Second, crystalloids were isolated from eosinophil granules by disruption in 0.1% Triton X-100 and centrifugation through a cushion of 50% sucrose. Highly purified core preparations yielded essentially a single band when analyzed by electrophoresis on polyacrylamide gels containing 1% sodium dodecyl sulfate (SDS). The E1%1cm of the core protein was 26.8 +/- 1.0 (X +/- SEM); the E1%1cm for the MBP was 26.3. The core protein could not be distinguished from the MBP by radioimmunoassay (RIA) and essentially all of the protein in the core preparations could be accounted for as MBP. The results indicate that the MBP is contained in the core of the guinea pig eosinophil granule and that it is probably the only protein present in the core.
利用免疫电子显微镜和颗粒晶体的分离技术,对豚鼠嗜酸性粒细胞主要碱性蛋白(MBP)在细胞内的定位进行了研究。首先,通过免疫过氧化物酶电子显微镜,我们发现嗜酸性粒细胞颗粒的MBP包含在颗粒的晶体核心内。在双抗体染色程序中,当使用兔抗MBP血清作为第一阶段抗体时,核心出现特异性染色,而当使用正常兔血清作为第一阶段抗体时则未见染色。其次,通过在0.1% Triton X-100中破碎并通过50%蔗糖垫层离心,从嗜酸性粒细胞颗粒中分离出晶体。当在含有1%十二烷基硫酸钠(SDS)的聚丙烯酰胺凝胶上进行电泳分析时,高度纯化的核心制剂产生了基本上单一的条带。核心蛋白的E1%1cm为26.8 +/- 1.0(X +/- SEM);MBP的E1%1cm为26.3。通过放射免疫分析(RIA)无法将核心蛋白与MBP区分开来,并且核心制剂中的基本上所有蛋白质都可被视为MBP。结果表明,MBP包含在豚鼠嗜酸性粒细胞颗粒的核心中,并且它可能是核心中唯一存在的蛋白质。