Hertzberg E L
In Vitro. 1980 Dec;16(12):1057-67. doi: 10.1007/BF02619256.
Studies on gap junctions isolated from rat liver by a procedure that avoids exogenous proteolysis (Hertzberg, E. L.; Gilula. N. B.; J. Biol. Chem. 254: 2138-2147; 1979) are described. The original isolation procedure was modified to increase the yield and has been extended to the preparation of gap junctions from mouse and bovine liver. Peptide map studies showed that the 27,000-dalton polypeptides present in liver gap junction preparations from all three sources are homologous and are not derived from other polypeptides of higher molecular weight that are observed in cruder preparations. Similar studies with lens fiber junctions demonstrated no homology between liver and lens junction polypeptides. Antibodies to the lens junction polypeptides did not cross-react with the liver gap junction polypeptide, further supporting this conclusion.
本文描述了通过避免外源性蛋白水解的方法从大鼠肝脏中分离间隙连接的研究(赫茨伯格,E.L.;吉卢拉,N.B.;《生物化学杂志》254: 2138 - 2147;1979)。对最初的分离方法进行了改进以提高产量,并已扩展到从小鼠和牛肝脏中制备间隙连接。肽图谱研究表明,来自所有这三种来源的肝脏间隙连接制剂中存在的27,000道尔顿的多肽是同源的,并非源自粗制剂中观察到的其他更高分子量的多肽。对晶状体纤维连接的类似研究表明,肝脏和晶状体连接多肽之间没有同源性。针对晶状体连接多肽的抗体与肝脏间隙连接多肽不发生交叉反应,进一步支持了这一结论。