Trifilieff E, Skalidis G, Hélynck G, Lepage P, Sorokine O, Van Dorsselaer A, Luu B
C R Acad Sci III. 1985;300(7):241-6.
By a combination of chromatographic methods, we have obtained in an apparently homogeneous state the 24 kDa "major myelin proteolipid" (MMPL) and the 20 kDa "myelin proteolipid" (DM-20). Contrary to a commonly held view, the second one is not a conformationally different form of its major companion, as it differs markedly by its amino-acid composition, its electrophoretic behaviour after performic acid oxidation, and the results of tryptic digestion; however, they are obviously very closely related, as shown by the selective cleavages at the level of methionines and tryptophanes. These results are most simply interpreted by a single deletion in DM-20 of the hydrophilic fragment 100-140 of the (known) structure of the 24 kDa proteolipid. Lees' hypothesis of a deletion of fragment 197-267 cannot be retained.
通过多种色谱方法的组合,我们以明显均一的状态获得了24 kDa的“主要髓鞘蛋白脂质”(MMPL)和20 kDa的“髓鞘蛋白脂质”(DM - 20)。与普遍观点相反,后者并非其主要同伴的构象不同形式,因为它在氨基酸组成、过甲酸氧化后的电泳行为以及胰蛋白酶消化结果方面存在显著差异;然而,正如甲硫氨酸和色氨酸水平的选择性裂解所示,它们显然密切相关。这些结果最简单的解释是,在DM - 20中,24 kDa蛋白脂质(已知)结构的亲水片段100 - 140发生了单一缺失。利斯关于片段197 - 267缺失的假设不能成立。