McDonald J A, Broekelmann T J, Kelley D G, Villiger B
J Biol Chem. 1981 Jun 10;256(11):5583-7.
Antisera against a Mr = 60,000 peptide containing the gelatin-binding domain of human plasma fibronectin (McDonald, J. A., and Kelley, D. G. (1980) J. Biol. Chem. 255, 8848-8858) bound the Mr = 60,000 peptide and intact fibronectin but not three other fragments released by leukocyte elastase proteinolysis (the Mr = 25,000 amino-terminal sequence, Mr = 140,000 sequence containing cell adhesive activity, and a Mr = 31,000 fragment). Affinity-purified Fab' blocked Mr = 60,000 peptide binding to gelatin and inhibited plasma and cellular fibronectin gelatin binding without affecting fibronectin-mediated cell spreading. In contrast, antifibronectin Fab' absorbed with the gelatin-binding fragment completely blocked fibronectin-mediated cell spreading. These data indicate that the gelatin-binding domain of fibronectin is immunogenic, and antisera against this domain recognize cellular fibronectin gelatin-binding sites. Inhibition of gelatin binding but not cell spreading by anti-gelatin binding domain Fab' confirms the hypothesis that fibronectin has separate sites mediating these activities. Selective inhibition of fibronectin-collagen binding by domain-specific antisera may help elucidate the role of fibronectin in organization of the extracellular matrix.
针对一种分子量为60,000的肽段(含人血浆纤连蛋白的明胶结合结构域,见麦克唐纳,J. A.,以及凯利,D. G.(1980年)《生物化学杂志》255卷,8848 - 8858页)的抗血清,能结合该分子量为60,000的肽段及完整的纤连蛋白,但不能结合白细胞弹性蛋白酶蛋白水解释放出的其他三个片段(分子量为25,000的氨基末端序列、含有细胞黏附活性的分子量为140,000的序列以及一个分子量为31,000的片段)。亲和纯化的Fab'可阻断分子量为60,000的肽段与明胶的结合,并抑制血浆和细胞纤连蛋白与明胶的结合,而不影响纤连蛋白介导的细胞铺展。相比之下,用明胶结合片段吸收的抗纤连蛋白Fab'则完全阻断了纤连蛋白介导的细胞铺展。这些数据表明,纤连蛋白的明胶结合结构域具有免疫原性,针对该结构域的抗血清可识别细胞纤连蛋白的明胶结合位点。抗明胶结合结构域Fab'抑制明胶结合但不抑制细胞铺展,这证实了纤连蛋白具有介导这些活性的独立位点这一假说。结构域特异性抗血清对纤连蛋白 - 胶原蛋白结合的选择性抑制,可能有助于阐明纤连蛋白在细胞外基质组织中的作用。