Baden H P, Jackson C E, Weiss L, Jimbow K, Lee L, Kubilus J, Gold R J
Am J Hum Genet. 1976 Sep;28(5):514-21.
The physicochemical properties of hair from a new recessive syndrome associated with brittle hair, intellectual impairment, decreased fertility, and short stature have been studied. Electrophoresis of the SCM-structural proteins showed that the alpha polypeptides appeared normal, but the matrix component was markedly reduced. This was confirmed by finding a normal alpha X-ray diffraction pattern but a reduced 1/2 cystine content of hair and an abnormal stress-strain curve. Electron-microscopic studies revealed extreme disorganization of the filaments which most likely resulted from the absence of normal cross-linking. Nails, which contain structural proteins similar to hair, also showed the abnormality. Since the matrix component seen by electrophoresis consists of more than one component the defect cannot be explained as a single structural gene abnormality.
对一种与脆发、智力障碍、生育力下降和身材矮小相关的新隐性综合征患者的头发进行了理化性质研究。对SCM结构蛋白进行电泳分析表明,α多肽看起来正常,但基质成分明显减少。这一点通过以下发现得到证实:头发的αX射线衍射图谱正常,但半胱氨酸含量降低,且应力-应变曲线异常。电子显微镜研究显示细丝极度紊乱,这很可能是由于缺乏正常交联所致。指甲含有与头发相似的结构蛋白,也表现出异常。由于电泳中观察到的基质成分由多种成分组成,因此不能将这种缺陷解释为单一结构基因异常。