Suehiro T, Yoshida K, Yamano T, Ohno F
Second Department of Internal Medicine, Kochi Medical School, Japan.
Jpn J Med. 1990 Nov-Dec;29(6):587-94. doi: 10.2169/internalmedicine1962.29.587.
A new variant of apolipoprotein E (apo E), named apo E-Kochi, was identified in the sera of a 29-year-old male with hyperlipoproteinemia as characterized by a broad-beta band. The characteristic double bands of apo E were seen in the isoelectric focusing gel of very low density lipoprotein from the proband and three members of his family. Of the double bands from the probands, the more cationic component was identical to ordinary apo E3 and the other anionic band was located at approximately a distance of one-half charge to the anode side. This anionic band is a new electrophoretical isoform of apo E (apo E-Kochi), and the molecular weight by sodium dodecyl sulfate electrophoresis and its antigenicity against anti apo E serum are the same as apo E3. Sequence analysis of lysyl endopeptidase fragments showed that apo E-Kochi differs from normal apo E3 at residue 145, where an arginine residue is substituted for histidine.
在一名29岁患有以宽β带为特征的高脂蛋白血症男性的血清中,鉴定出一种新的载脂蛋白E(apo E)变体,命名为apo E-高知。在该先证者及其家族三名成员的极低密度脂蛋白的等电聚焦凝胶中观察到了apo E的特征性双链。在先证者的双链中,阳离子性更强的成分与普通apo E3相同,另一条阴离子带位于距阳极侧约半个电荷的位置。这条阴离子带是apo E的一种新的电泳同工型(apo E-高知),其通过十二烷基硫酸钠电泳测得的分子量以及对抗apo E血清的抗原性与apo E3相同。赖氨酰内肽酶片段的序列分析表明,apo E-高知在第145位残基处与正常apo E3不同,该位置的组氨酸被精氨酸残基取代。