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蛋白激酶A可调节细胞内运输,它与细胞器上的分子马达形成复合物。

Protein kinase A, which regulates intracellular transport, forms complexes with molecular motors on organelles.

作者信息

Kashina Anna S, Semenova Irina V, Ivanov Pavel A, Potekhina Ekaterina S, Zaliapin Ilya, Rodionov Vladimir I

机构信息

University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06032-1507, USA.

出版信息

Curr Biol. 2004 Oct 26;14(20):1877-81. doi: 10.1016/j.cub.2004.10.003.

Abstract

Major signaling cascades have been shown to play a role in the regulation of intracellular organelle transport . Aggregation and dispersion of pigment granules in melanophores are regulated by the second messenger cAMP through the protein kinase A (PKA) signaling pathway ; however, the exact mechanisms of this regulation are poorly understood. To study the role of signaling molecules in the regulation of pigment transport in melanophores, we have asked the question whether the components of the cAMP-signaling pathway are bound to pigment granules and whether they interact with molecular motors to regulate the granule movement throughout the cytoplasm. We found that purified pigment granules contain PKA and scaffolding proteins and that PKA associates with pigment granules in cells. Furthermore, we found that the PKA regulatory subunit forms two separate complexes, one with cytoplasmic dynein ("aggregation complex") and one with kinesin II and myosin V ("dispersion complex"), and that the removal of PKA from granules causes dissociation of dynein and disruption of dynein-dependent pigment aggregation. We conclude that cytoplasmic organelles contain protein complexes that include motor proteins and signaling molecules involved in different components of intracellular transport. We propose to call such complexes 'regulated motor units' (RMU).

摘要

主要的信号级联反应已被证明在细胞内细胞器运输的调节中发挥作用。黑素细胞中色素颗粒的聚集和分散是由第二信使环磷酸腺苷(cAMP)通过蛋白激酶A(PKA)信号通路调节的;然而,这种调节的确切机制尚不清楚。为了研究信号分子在黑素细胞色素运输调节中的作用,我们提出了一个问题,即cAMP信号通路的成分是否与色素颗粒结合,以及它们是否与分子马达相互作用以调节颗粒在整个细胞质中的运动。我们发现纯化的色素颗粒含有PKA和支架蛋白,并且PKA在细胞中与色素颗粒相关联。此外,我们发现PKA调节亚基形成两个独立的复合物,一个与细胞质动力蛋白(“聚集复合物”)结合,另一个与驱动蛋白II和肌球蛋白V(“分散复合物”)结合,并且从颗粒中去除PKA会导致动力蛋白解离并破坏依赖动力蛋白的色素聚集。我们得出结论,细胞质细胞器含有蛋白质复合物,这些复合物包括参与细胞内运输不同成分的马达蛋白和信号分子。我们建议将这种复合物称为“调节运动单元”(RMU)。

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