首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >The energy relay: a proofreading scheme based on dynamic cooperativity and lacking all characteristic symptoms of kinetic proofreading in DNA replication and protein synthesis.
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The energy relay: a proofreading scheme based on dynamic cooperativity and lacking all characteristic symptoms of kinetic proofreading in DNA replication and protein synthesis.

机译:能量继电器:一种基于动态合作性的校对方案在DNA复制和蛋白质合成中缺乏动力学校对的所有特征性症状。

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摘要

A mechanism for proofreading biosynthetic processes requiring high accuracy is described. The previously understood "kinetic proofreading" mechanism of enhancing accuracy has distinguishing characteristics such as the non-stoichiometric use of substrate or cosubstrate that have allowed its identification in aspects of DNA and protein synthesis. The proofreading scheme developed here, though generically related, lacks all the previous identifying features. A DNA polymerase proofreading in this manner need neither generate dNMP nor have a 3' leads to 5' exonuclease activity. Protein synthesis could be proofread even with stoichiometric GTP consumption or without elongation factor Tu . GTP. The kinetic scheme that generates this proofreading makes use of an "energy relay" from previous substrate molecules and is a representative of a class of nonequilibrium processes displaying dynamic cooperativity. This proofreading mechanism has its own identifying characteristics, which are sufficiently subtle that they would have generally escaped notice or defied interpretation.
机译:描述了用于校对需要高精度的生物合成过程的机制。先前理解的提高精确度的“动力学校对”机制具有明显的特征,例如底物或共底物的非化学计量使用,这使得可以在DNA和蛋白质合成方面进行鉴定。尽管这里开发的校对方案具有一般性的关联性,但它缺少所有以前的识别功能。以这种方式校对的DNA聚合酶既不需要产生dNMP,也不需要3'导致5'核酸外切酶活性。即使消耗化学计量的GTP或不使用延伸因子Tu,蛋白质合成也可以得到校对。 GTP。产生这种校对的动力学方案利用了来自先前底物分子的“能量中继”,并且是显示动态协同性的一类非平衡过程的代表。这种校对机制具有自己的识别特征,这些特征非常微妙,以至于通常不会引起注意或反抗。

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