Tobe T, Higashi T
J Biochem. 1980 Nov;88(5):1341-7. doi: 10.1093/oxfordjournals.jbchem.a133102.
We reinvestigated the site of synthesis of rat liver catalase, and it has been reconfirmed that catalase is synthesized not only by free polysomes but also by membrane-bound polysomes. Considerable amounts of nascent catalase on rough microsomes were released from the membrane into the medium upon incubation with puromycin, not transported directly into the intracisternal cavity of microsomes. On the other hand, catalase newly synthesized in vitro was shown to be segregated by stripped rat liver microsomal membranes in a state resistant to proteolysis. Since this segregation occurred without coupled protein synthesis, catalase appears to be transported by a mechanism different from co-translational transfer. A hypothesis is presented regarding the mechanism of intracellular transport of liver catalase.
我们重新研究了大鼠肝脏过氧化氢酶的合成位点,现已再次证实过氧化氢酶不仅由游离多核糖体合成,也由膜结合多核糖体合成。在用嘌呤霉素孵育时,粗面微粒体上相当数量的新生过氧化氢酶从膜上释放到培养基中,而不是直接转运到微粒体的潴泡腔内。另一方面,体外新合成的过氧化氢酶被去垢的大鼠肝脏微粒体膜以抗蛋白酶水解的状态分隔开来。由于这种分隔在没有偶联蛋白质合成的情况下发生,过氧化氢酶似乎是通过一种不同于共翻译转运的机制进行转运的。本文提出了一个关于肝脏过氧化氢酶细胞内转运机制的假说。