Conde R D, Scornik O A
Biochem J. 1977 Jul 15;166(1):115-21. doi: 10.1042/bj1660115.
A study is presented of the liver protein gain during the early stages of postnatal development. Fractional rates of protein synthesis and degradation were determined in vivo in livers of 4-day-old mice. At this age, liver protein accumulated at a rate of 18% per day. Synthesis was measured after the injection of massive amounts of radioactive leucine. Degradation was extimated as the balance between synthesis and accumulation of stable liver proteins, or from the disappearance of radioactivity from liver protein previously labelled by the administration of NaH14CO3. We found that the neonatal livers: (1) synthesize 139% as much protein per unit time and unit mass as adult tissue, which is accounted for by a higher ribosome concentration (synthesis per mg of RNA was the same); (2) retain 39% of the newly synthesized protein as stable liver components (compared with 48% in adult mice); (3) degrade protein at 56% of the rate in the adult liver. This lower rate of degradation is quantitatively the most significant difference between the growing and non-growing liver.
本文呈现了一项关于出生后发育早期肝脏蛋白质增加情况的研究。测定了4日龄小鼠肝脏中蛋白质合成与降解的分数率。在这个年龄段,肝脏蛋白质以每天18%的速率积累。在注射大量放射性亮氨酸后测量合成情况。降解量通过稳定肝脏蛋白质的合成与积累之间的平衡来估算,或者根据先前通过给予NaH¹⁴CO₃标记的肝脏蛋白质中放射性的消失情况来估算。我们发现新生肝脏:(1)每单位时间和单位质量合成的蛋白质是成年组织的139%,这是由更高的核糖体浓度导致的(每毫克RNA的合成量相同);(2)将新合成蛋白质的39%保留为稳定的肝脏成分(成年小鼠为48%);(3)蛋白质降解速率为成年肝脏的56%。这种较低的降解速率在数量上是生长中的肝脏和非生长中的肝脏之间最显著的差异。