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真核起始因子4D(eIF-4D)的hypusine修饰或丰度变化与HeLa细胞中的翻译抑制无关。

Changes in eIF-4D hypusine modification or abundance are not correlated with translational repression in HeLa cells.

作者信息

Duncan R F, Hershey J W

出版信息

J Biol Chem. 1986 Sep 25;261(27):12903-6.

PMID:3091607
Abstract

Initiation factor eIF-4D is represented by about 11 X 10(6) molecules/HeLa cell (0.45% of the cytoplasmic protein molecules). The fraction of eIF-4D that contains the post-translational modification of lysine converted to hypusine is not regulated with respect to translation rate in HeLa cells. It is proportional to the rate of eIF-4D synthesis in exponentially growing cells (maximal protein synthesis rates) as well as in serum-depleted cells (protein synthesis rates depressed about 6-8-fold). In cells in which protein synthesis is arrested by cycloheximide, no hypusine addition or exchange is detected. During rapid repressions of protein synthesis due to either heat shock or hypertonic shock there is no change in the extent of eIF-4D containing hypusine. These results are most consistent with an eIF-4D biogenesis in which all molecules are modified to contain hypusine during or shortly after the translation process itself, and the modification state is not regulated thereafter.

摘要

起始因子eIF - 4D在每个海拉细胞中约有11×10⁶个分子(占细胞质蛋白分子的0.45%)。在海拉细胞中,含有经翻译后修饰赖氨酸转化为hypusine的eIF - 4D部分,其含量不受翻译速率的调节。它与指数生长细胞(最大蛋白质合成速率)以及血清饥饿细胞(蛋白质合成速率降低约6 - 8倍)中eIF - 4D的合成速率成正比。在用环己酰亚胺使蛋白质合成停滞的细胞中,未检测到hypusine的添加或交换。在因热休克或高渗休克导致蛋白质合成快速抑制期间,含有hypusine的eIF - 4D的程度没有变化。这些结果与eIF - 4D的生物合成最为一致,即在翻译过程中或之后不久,所有分子都被修饰为含有hypusine,且此后修饰状态不再受调节。

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