Chan L S, Wang X S, Lapiere J C, Marinkovich M P, Jones J C, Woodley D T
Department of Dermatology, Northwestern University Medical School, Chicago, Illinois 60611-3010, USA.
J Invest Dermatol. 1995 Jul;105(1):75-9. doi: 10.1111/1523-1747.ep12313340.
A 105-kD lower lamina lucida antigen (p105) has been detected by autoantibodies (anti-p105) from patients with a novel immunobullous disease. To distinguish p105 from other known lamina lucida components, we performed comparative immunoblotting on purified human amniotic laminin-5 (kalinin), 804G matrix (enriched in laminin-5), and keratinocyte and fibroblast proteins using anti-804G matrix antibody (J-18) and anti-p105. J-18 labeled the truncated laminin-5 gamma 2 chain in amniotic laminin-5, 804G matrix, and keratinocyte conditioned medium, but did not label fibroblast cytosol. Conversely, anti-p105 did not label amniotic laminin-5 or 804G matrix, but did label p105 in both keratinocyte conditioned medium and fibroblast cytosol. J-18 labeled the 105-kD laminin-5 gamma 2 chain in reduced keratinocyte proteins and a 400-kD laminin-5 complex under non-reducing conditions. In contrast, anti-p105 labeled p105 under both reducing and non-reducing conditions but did not label a 400-kD protein complex. Similarly, comparative immunoblotting on keratinocyte proteins using anti-p105 and anti-laminin-1 revealed no commonly labeled protein bands. Electrophoretic fractionations by preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting of these fractions revealed that the peak fractions of keratinocyte proteins reactive with anti-p105 are different from those reactive with J-18. Furthermore, keratinocyte proteins fractionated by Mono Q anion-exchange chromatography revealed fractions immunoreactive with anti-p105, whereas J-18 showed no reactivity with these fractions. Two-dimensional gel electrophoresis and immunoblotting with anti-p105 revealed p105 to be an acidic protein with isoelectric points between 5.7 and 6.3, distinct from the isoelectric points of laminin-5 gamma 2 chain. We conclude that p105 is an acidic protein located in the lamina lucida and distinct from the truncated laminin-5 gamma 2 chain and the laminin-1 family.
一种新型免疫性大疱性疾病患者的自身抗体(抗 - p105)检测到一种105-kD的透明层下抗原(p105)。为了将p105与其他已知的透明层成分区分开来,我们使用抗804G基质抗体(J - 18)和抗 - p105对纯化的人羊膜层粘连蛋白 - 5(kalinin)、804G基质(富含层粘连蛋白 - 5)以及角质形成细胞和成纤维细胞蛋白进行了比较免疫印迹分析。J - 18标记了羊膜层粘连蛋白 - 5、804G基质和角质形成细胞条件培养基中的截短层粘连蛋白 - 5γ2链,但未标记成纤维细胞胞质溶胶。相反,抗 - p105未标记羊膜层粘连蛋白 - 5或804G基质,但标记了角质形成细胞条件培养基和成纤维细胞胞质溶胶中的p105。J - 18在还原条件下标记了角质形成细胞蛋白中的105-kD层粘连蛋白 - 5γ2链,在非还原条件下标记了一个400-kD的层粘连蛋白 - 5复合物。相比之下,抗 - p105在还原和非还原条件下均标记p105,但未标记400-kD的蛋白复合物。同样,使用抗 - p105和抗层粘连蛋白 - 1对角质形成细胞蛋白进行比较免疫印迹分析,未发现共同标记的蛋白条带。通过制备性十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳对这些蛋白进行电泳分离并对分离组分进行免疫印迹分析,结果显示与抗 - p105反应的角质形成细胞蛋白的峰值组分与与J - 18反应的不同。此外,通过Mono Q阴离子交换色谱法分离的角质形成细胞蛋白显示出与抗 - p105反应的组分,而J - 18对这些组分无反应。二维凝胶电泳和用抗 - p105进行免疫印迹分析显示p105是一种酸性蛋白,其等电点在5.7至6.3之间,与层粘连蛋白 - 5γ2链的等电点不同。我们得出结论,p105是一种位于透明层的酸性蛋白,与截短的层粘连蛋白 - 5γ2链和层粘连蛋白 - 1家族不同。