Yoshiike T, Woodley D T, Briggaman R A
Department of Dermatology, University of North Carolina, School of Medicine, Chapel Hill 27514.
J Invest Dermatol. 1988 Feb;90(2):127-33. doi: 10.1111/1523-1747.ep12462092.
To clarify the relationship of the 290 and 145 kDa chains of the epidermolysis bullosa acquisita (EBA) antigen, we subjected urea extracts of skin basement membrane zone (BMZ) proteins and isolated 290 and 145 kDa chains of the EBA antigen cut out of sodium dodecyl sulfate polyacrylamide gels to treatment with clostridial collagenase. When the reaction products were electrophoresed, transblotted, and reacted with EBA patient sera or two monoclonal antibodies to the EBA antigen, the 290 kDa chain was degraded into the 145 kDa band that was resistant to cleavage with collagenase. The 145 kDa domain, isolated after collagenase treatment of the whole BMZ extract, was resistant to degradation by hyaluronidase, chondroitinase ABC, heparinase, and heparitinase but was readily degraded by V-8 protease. These data suggest that the EBA antigen consists of collagen and noncollagen domains of identical size (Mr 145,000), and that the 145 kDa noncollagen domain is generated via degradation of the native 290 kDa species by collagenase.
为阐明获得性大疱性表皮松解症(EBA)抗原的290 kDa和145 kDa链之间的关系,我们对皮肤基底膜带(BMZ)蛋白的尿素提取物进行处理,并将从十二烷基硫酸钠聚丙烯酰胺凝胶中切下的EBA抗原的290 kDa和145 kDa链用梭菌胶原酶处理。当反应产物进行电泳、转印并与EBA患者血清或两种抗EBA抗原的单克隆抗体反应时,290 kDa链被降解为对胶原酶切割具有抗性的145 kDa条带。在对整个BMZ提取物进行胶原酶处理后分离出的145 kDa结构域,对透明质酸酶、软骨素酶ABC、肝素酶和硫酸乙酰肝素酶的降解具有抗性,但很容易被V-8蛋白酶降解。这些数据表明,EBA抗原由大小相同(Mr 145,000)的胶原结构域和非胶原结构域组成,并且145 kDa非胶原结构域是通过胶原酶对天然290 kDa分子的降解产生的。