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远距离信号传递:单细胞内的梯度模式和磷酸化波。

Signalling over a distance: gradient patterns and phosphorylation waves within single cells.

机构信息

Systems Biology Ireland, University College Dublin, Belfield, Dublin 4, Ireland.

出版信息

Biochem Soc Trans. 2010 Oct;38(5):1235-41. doi: 10.1042/BST0381235.

Abstract

Recent discoveries of phosphorylation gradients and microdomains with different protein activities have revolutionized our perception of information transfer within single cells. The different spatial localization of opposing reactions in protein-modification cycles has been shown to bring about heterogeneous stationary patterns and travelling waves of protein activities. We review spatial patterns and modes of signal transfer through phosphorylation/dephosphorylation and GDP/GTP exchange cycles and cascades. We show how switches between low-activity and high-activity states in a bistable activation-deactivation cycle can initiate the propagation of travelling protein-modification waves in the cytoplasm. Typically, an activation wave is initiated at the plasma membrane and propagates through the cytoplasm until it reaches the nucleus. An increase in deactivator activity is followed by the initiation of an inactivation wave that moves in the reverse direction from the nucleus. We show that the ratio of opposing enzyme rates is a key parameter that controls both the spread of activation through cascades and travelling waves.

摘要

最近发现的磷酸化梯度和具有不同蛋白质活性的微区彻底改变了我们对单个细胞内信息传递的认识。已经证明,在蛋白质修饰循环中,相反反应的不同空间定位会导致蛋白质活性的不均匀稳定模式和移动波。我们回顾了通过磷酸化/去磷酸化和 GDP/GTP 交换循环和级联进行信号传递的空间模式和方式。我们展示了在双稳态激活-失活循环中从低活性状态到高活性状态的转换如何引发细胞质中蛋白质修饰波的传播。通常,激活波在质膜处起始,并在细胞质中传播,直到它到达细胞核。去激活剂活性的增加随后引发了从核反向移动的失活波。我们表明,相反酶活性的比率是控制级联和移动波中激活传播的关键参数。

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