Owen P, Kaback H R
Biochemistry. 1979 Apr 17;18(8):1422-6. doi: 10.1021/bi00575a005.
The antigenic architecture of membrane vesicles prepared from Escherichia coli ML 308--225 has been studied using crossed immunoelectrophoresis. Progressive immunoadsorption experiments conducted with control vesicles and with physically disrupted vesicles were used to monitor and quantitate the expression of 14 different immunogens. Eleven immunogens, including NADH dehydrogenase (EC 1.6.33.3), D-lactate dehydrogenase (EC 1.1.1.27), dihydro-orotate dehydrogenase (EC 1.3.3.1), 6-phosphogluconate dehydrogenase (EC 1.1.1.43), polynucleotide phosphorylase (EC 2.3.7.8), and beta-galactosidase (EC 3.2.1.23), exhibit minimal expression (10% or less) unless the vesicles are disrupted. Three unidentified antigens are expressed to a similar extent in untreated and disrupted vesicles. Consideration of these and other results [Owen, P., & Kaback, H. R. (1978) Proc. Natl. Acad. Sci. U.S.A. 75, 3148] in terms of membrane polarity, dislocation of antigens, and possible transmembrane orientation of some immunogens reveals that over 95% of the membrane in the vesicle preparations is in the form of sealed sacculi with the same orientation as the intact cell. Furthermore, antigens are distributed across the membrane in a highly asymmetric manner, indicating that dislocation of components from the inner to the outer surface of the membrane during vesicle preparation does not occur to an extent exceeding 10%.
利用交叉免疫电泳技术研究了从大肠杆菌ML 308 - 225制备的膜泡的抗原结构。用对照膜泡和物理破碎的膜泡进行的逐步免疫吸附实验,用于监测和定量14种不同免疫原的表达。11种免疫原,包括NADH脱氢酶(EC 1.6.33.3)、D - 乳酸脱氢酶(EC 1.1.1.27)、二氢乳清酸脱氢酶(EC 1.3.3.1)、6 - 磷酸葡萄糖酸脱氢酶(EC 1.1.1.43)、多核苷酸磷酸化酶(EC 2.3.7.8)和β - 半乳糖苷酶(EC 3.2.1.23),除非膜泡被破坏,否则表达极少(10%或更低)。三种未鉴定的抗原在未处理和破碎的膜泡中表达程度相似。根据膜极性、抗原错位以及一些免疫原可能的跨膜方向来考虑这些及其他结果[欧文,P.,& 卡巴克,H. R.(1978年)美国国家科学院院刊75,3148],发现膜泡制剂中超过95%的膜呈密封囊泡形式,其方向与完整细胞相同。此外,抗原在膜上的分布高度不对称,这表明在膜泡制备过程中,成分从膜的内表面向外表面的错位程度不超过10%。