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Long-range signaling by phosphoprotein waves arising from bistability in protein kinase cascades

机译:蛋白激酶级联中的双稳性引起的磷蛋白波的远程信号传导

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摘要

A hallmark of protein kinase/phosphatase cascades, including mitogen-activated protein kinase (MAPK) pathways, is the spatial separation of their components within cells. The top-level kinase, MAP3K, is phosphorylated at the cell membrane, and cytoplasmic kinases at sequential downstream levels (MAP2K and MAPK) spread the signal to distant targets. Given measured protein diffusivity and phosphatase activities, signal propagation by diffusion would result in a steep decline of MAP2K activity and low bisphosphorylated MAPK (ppMAPK) levels near the nucleus, especially in large cells, such as oocytes. Here, we show that bistability in a two-site MAPK (de)phosphorylation cycle generates a novel type of phosphoprotein wave that propagates from the surface deep into the cell interior. Positive feedback from ppMAPK to cytoplasmic MAP2K enhances the propagation span of the ppMAPK wave, making it possible to convey phosphorylation signals over exceedingly long distances. The finding of phosphorylation waves traveling with constant amplitude and high velocity may solve a long-standing enigma of survival signaling in developing neurons.
机译:包括有丝分裂原激活的蛋白激酶(MAPK)途径在内的蛋白激酶/磷酸酶级联反应的标志是它们在细胞内的空间分离。最高水平的激酶MAP3K在细胞膜上被磷酸化,并且在下游连续水平(MAP2K和MAPK)的胞质激酶将信号传播到远处的靶标。给定测量的蛋白质扩散性和磷酸酶活性,通过扩散进行的信号传播将导致MAP2K活性急剧下降,并且靠近细胞核的双磷酸化MAPK(ppMAPK)水平降低,尤其是在大细胞(如卵母细胞)中。在这里,我们表明,在两个位点的MAPK(去磷酸化)循环中的双稳态产生了一种新型的磷蛋白波,该磷蛋白波从表面传播到细胞内部。从ppMAPK到细胞质MAP2K的正反馈增强了ppMAPK波的传播范围,从而可以在非常长的距离上传递磷酸化信号。发现以恒定幅度和高速度传播的磷酸化波可以解决发育中神经元中生存信号的长期谜团。

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