Ogawa H, Hattori M, Ishibashi Y
Arch Dermatol Res. 1979 Oct;266(2):109-16. doi: 10.1007/BF00694618.
The fibrous protein of stratum corneum was isolated from a patient with bullous congenital ichthyosiform erythroderma (BCIE), and its properties characterized using electron microscopy, amino acid analysis and SDS gel electrophoresis. Results were compared with the characteristics of the fibrous protein isolated from stratum corneum of normal controls. From 900 mg (dry weight) of stratum corneum, 68 mg of fibrous protein was obtained from the patient, while 178 mg was obtained from the normal control. Structural differences were observed with electron microscopy and chemical differences, were shown in the ratio of several amino acids. On SDS electrophoresis, the 55,000 dalton constituent of normal fibrous protein could not be identified in the fibrous protein from this patient. These results suggest that an alteration of the polypeptide composition of fibrous protein from this patient with BCIE occurred, and this alteration induced the morphological and clinical features of this dominant genetic keratinization disorder.
从一名大疱性先天性鱼鳞病样红皮病(BCIE)患者的角质层中分离出纤维蛋白,并使用电子显微镜、氨基酸分析和SDS凝胶电泳对其特性进行表征。将结果与从正常对照角质层中分离出的纤维蛋白的特性进行比较。从900毫克(干重)角质层中,患者获得了68毫克纤维蛋白,而正常对照获得了178毫克。通过电子显微镜观察到结构差异,并且几种氨基酸的比例显示出化学差异。在SDS电泳中,该患者纤维蛋白中无法鉴定出正常纤维蛋白的55,000道尔顿成分。这些结果表明,该BCIE患者的纤维蛋白多肽组成发生了改变,并且这种改变导致了这种显性遗传性角化障碍的形态学和临床特征。