Atassi M Z
Eur J Biochem. 1984 Nov 15;145(1):1-20. doi: 10.1111/j.1432-1033.1984.tb08516.x.
Studies in this laboratory have resulted in the delineation and synthetic verification of several complete protein antigenic structures that are recognized by antibodies. More recently, for the first time, the full profiles of the sites that are recognized by T cells have been localized and confirmed by synthesis for two proteins, myoglobin and lysozyme. These have thus far constituted the only complete antigenic structures to be determined. The availability of these antigenic structures has enabled us to investigate in detail the molecular and cellular parameters responsible for immune recognition, responses to, and control and regulation of these responses to protein antigens at the molecular and submolecular levels. Moreover, these investigations have afforded general strategies for the synthetic mimicking of not only antigenic sites, but also protein binding sites involved in other biological activities.
本实验室的研究已确定并通过合成验证了几种完整的蛋白质抗原结构,这些结构可被抗体识别。最近,首次对两种蛋白质——肌红蛋白和溶菌酶——被T细胞识别的位点进行了全面定位,并通过合成予以确认。迄今为止,这些是仅有的已确定的完整抗原结构。这些抗原结构的可得性使我们能够在分子和亚分子水平上详细研究负责免疫识别、对蛋白质抗原的反应以及对这些反应的控制和调节的分子和细胞参数。此外,这些研究不仅为抗原位点的合成模拟,也为参与其他生物活性的蛋白质结合位点的合成模拟提供了通用策略。