Mulac-Jericević B, Kurisaki J, Atassi M Z
Proc Natl Acad Sci U S A. 1987 Jun;84(11):3633-7. doi: 10.1073/pnas.84.11.3633.
Reaction of overlapping synthetic peptides spanning the extracellular part (residues 1-210) of the alpha chain of the Torpedo californica acetylcholine receptor (an alpha 2 beta gamma delta pentamer) with anti-receptor antibodies produced the profiles of the continuous antigenic regions of the correlate segment. Essentially similar profiles were recognized by rabbit and outbred mouse antibodies against isolated receptor or mouse antibodies against membrane-bound receptor. The antigenic sites reside within eight continuous regions: residues 1-14, 25-36, 41-53, 63-75, 102-114, 128-138, 172-182, and 188-198. Five of these regions (the second and the fifth through the eighth) appeared to be immunodominant. Significantly, two of these antigenic regions (i.e., those residing within residues 128-138 and 188-198) coincided with known toxin-binding regions. The antigenic profile suggests that recognition is directed to the intact molecule and only very slightly to the processed (fragmented) protein.
用电鳐乙酰胆碱受体α链(一种α₂βγδ五聚体)胞外部分(第1至210位氨基酸残基)的重叠合成肽与抗受体抗体反应,得到了相关片段连续抗原区域的图谱。针对分离受体的兔抗体和远交系小鼠抗体,以及针对膜结合受体的小鼠抗体,识别出了基本相似的图谱。抗原位点位于八个连续区域:第1至14位氨基酸残基、第25至36位氨基酸残基、第41至53位氨基酸残基、第63至75位氨基酸残基、第102至114位氨基酸残基、第128至138位氨基酸残基、第172至182位氨基酸残基以及第188至198位氨基酸残基。其中五个区域(第二个区域以及第五至第八个区域)似乎是免疫显性的。值得注意的是,这些抗原区域中的两个(即位于第128至138位氨基酸残基和第188至198位氨基酸残基内的区域)与已知的毒素结合区域重合。抗原图谱表明,识别作用针对的是完整分子,而对加工后的(片段化的)蛋白质的识别作用非常微弱。