Boucher A, Bernard N, Miller A, Rodien P, Salvi M, Wall J R
Thyroid Studies Center, Montreal General Hospital, Quebec, Canada.
J Endocrinol Invest. 1994 Jan;17(1):7-13. doi: 10.1007/BF03344954.
Among the candidate eye muscle autoantigens proposed as being relevant to the pathogenesis of thyroid-associated ophthalmopathy (TAO), a 64 kDa membrane autoantigen appears to be most closely associated with the eye disorder. We have examined the tissue localization and some of the physicochemical properties of this molecule in 3 human tissues, namely thyroid (THY), eye muscle (EM) and skeletal muscle (SKE), and in pig eye muscle (PEM), by two-dimensional (2-D) [isoelectric focusing (IEF)/sodium dodecyl polyacrylamide gel electrophoresis (SDS-PAGE)] gel electrophoresis followed by Western blotting. Antibody probes used were whole sera from patients with TAO and antibodies affinity purified from TAO sera by binding to, and elution from, a sepharose-4B column conjugated with D1, a 98 amino acid peptide fragment of a recombinant 64 kDa thyroid autoantigen. Soluble membrane proteins eluted from a slice of SDS-PAGE gel containing 60-70 kDa material was prepared from the four tissues and used as antigen for 2-D gel separation. The presence of a 64 kDa antigen in THY and EM recognized by sera from patients with TAO, but only rarely by those from normal individuals, was confirmed. Pretreatment of the eluted 60-70 kDa material with N-Glycosidase F to eliminate charge heterogeneity resulting from glycosylation differences, changed the pI and MW of molecules recognized by TAO sera, in THY and EM. This suggests that the 64 kDa molecule(s) in EM and THY targeted by sera from patients with TAO are glycoproteins and that they are different in the two tissues.(ABSTRACT TRUNCATED AT 250 WORDS)
在被认为与甲状腺相关眼病(TAO)发病机制相关的候选眼肌自身抗原中,一种64 kDa的膜自身抗原似乎与该眼部疾病关系最为密切。我们通过二维(2-D)[等电聚焦(IEF)/十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)]凝胶电泳,随后进行蛋白质印迹法,检测了该分子在3种人体组织,即甲状腺(THY)、眼肌(EM)和骨骼肌(SKE)以及猪眼肌(PEM)中的组织定位和一些物理化学性质。所用的抗体探针是TAO患者的全血清以及通过与结合有重组64 kDa甲状腺自身抗原的98个氨基酸肽片段D1的琼脂糖-4B柱结合并洗脱而从TAO血清中亲和纯化的抗体。从这四种组织中制备了从含有60 - 70 kDa物质的SDS-PAGE凝胶切片上洗脱的可溶性膜蛋白,并用作二维凝胶分离的抗原。证实了TAO患者血清能识别THY和EM中存在的64 kDa抗原,而正常个体的血清很少能识别。用N-糖苷酶F对洗脱的60 - 70 kDa物质进行预处理以消除糖基化差异导致的电荷异质性,改变了THY和EM中TAO血清识别的分子的pI和MW。这表明TAO患者血清靶向的EM和THY中的64 kDa分子是糖蛋白,并且它们在两种组织中有所不同。(摘要截短至250字)