Lambris J D, Ross G D
J Exp Med. 1982 May 1;155(5):1400-11. doi: 10.1084/jem.155.5.1400.
Antibody to the binding site (idiotype) of anti-factor H was shown to have specificity for both B lymphocyte membrane H receptors and C3b. Goat F(ab')(2) anti-human H was purified by absorption and elution from H agarose and used for rabbit immunization to produce anti-anti-H (aaH). After absorption with nonimmune goat IgG, (125)I-labeled aaH bound to B lymphocytes and to sheep erythrocytes coated with C3b (EC3b) but did not bind to T lymphocytes or to EC3d. All B cell- and C3b-specific activities of the aaH were removed and subsequently recovered by absorption and elution of the antibody from either C3-agarose or goat-anti-H-agarose. This indicated that the aaH probably recognized a single common antigenic structure that was shared by anti-H, C3b, and the membranes of B cells. Affinity-purified aaH resembled H in that it bound to B cells, blocked the uptake of H onto B cell H receptors, and triggered B cells to release endogenous factor I (C3b inactivator). In addition, aaH functioned with factor I as either a cofactor for cleavage of fluid-phase C3b or a potentiator for cleavage of bound C3b. This same spectrum of C3 binding functions could not be demonstrated with either sheep anti-C3b or rabbit-anti-C3c. Analysis by sodium dodecyl sulfate- polyacrylamide get electrophoresis of the [(3)H]leucine intrinsically labeled B cell proteins reactive with the purified aaH revealed proteins of 100,000 M(r) and 50,000 M(r) without reduction, and after complete reduction of disulfide bonds, a single protein band of 50,000 M(r). This same protein molecular weight profile was also demonstrated with labeled B cell proteins that were absorbed and eluted from H-agarose. Thus, aaH is apparently specific for both B cell H receptors and C3b. However, because parallel analysis of C3b confirmed its known 115,000- and 75,000-M(r) polypeptide chain structure, the H receptor is probably not C3b and shares only the structure of the H binding site with C3b.
抗抗因子H(aaH)的结合位点(独特型)抗体显示出对B淋巴细胞膜H受体和C3b均具有特异性。山羊F(ab')(2)抗人H通过从H琼脂糖上吸收和洗脱进行纯化,并用于兔免疫以产生抗抗H(aaH)。在用非免疫山羊IgG吸收后,(125)I标记的aaH与B淋巴细胞以及包被有C3b的绵羊红细胞(EC3b)结合,但不与T淋巴细胞或EC3d结合。aaH的所有B细胞特异性和C3b特异性活性通过从C3 - 琼脂糖或山羊抗H - 琼脂糖上吸收和洗脱抗体而被去除,随后又得以恢复。这表明aaH可能识别一种由抗H、C3b和B细胞膜共享的单一共同抗原结构。亲和纯化的aaH与H相似,它能与B细胞结合,阻断H与B细胞H受体的结合,并触发B细胞释放内源性因子I(C3b灭活剂)。此外,aaH与因子I一起作为液相C3b裂解的辅因子或结合型C3b裂解的增强剂发挥作用。绵羊抗C3b或兔抗C3c均未表现出相同的C3结合功能谱。用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分析与纯化的aaH反应的[(3)H]亮氨酸内在标记的B细胞蛋白,未还原时显示出分子量为100,000和50,000的蛋白,在二硫键完全还原后,出现一条分子量为50,000的单一蛋白带。从H - 琼脂糖上吸收和洗脱的标记B细胞蛋白也显示出相同的蛋白质分子量谱。因此,aaH显然对B细胞H受体和C3b均具有特异性。然而,由于对C3b的平行分析证实了其已知的115,000和75,000分子量的多肽链结构,H受体可能不是C3b,仅与C3b共享H结合位点的结构。