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Intracellular Transport and Kinesin Superfamily Proteins, KIFs: Structure, Function, and Dynamics.

机译:细胞内转运和驱动蛋白超家族蛋白,KIFs:结构,功能和动力学。

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Various molecular cell biology and molecular genetic approaches have indicated significant roles for kinesin superfamily proteins (KIFs) in intracellular transport and have shown that they are critical for cellular morphogenesis, functioning, and survival. KIFs not only transport various membrane organelles, protein complexes, and mRNAs for the maintenance of basic cellular activity, but also play significant roles for various mechanisms fundamental for life, such as brain wiring, higher brain functions such as memory and learning and activity-dependent neuronal survival during brain development, and for the determination of important developmental processes such as left-right asymmetry formation and suppression of tumorigenesis. Accumulating data have revealed a molecular mechanism of cargo recognition involving scaffolding or adaptor protein complexes. Intramolecular folding and phosphorylation also regulate the binding activity of motor proteins. New techniques using molecular biophysics, cryoelectron microscopy, and X-ray crystallography have detected structural changes in motor proteins, synchronized with ATP hydrolysis cycles, leading to the development of independent models of monomer and dimer motors for processive movement along microtubules.
机译:各种分子细胞生物学和分子遗传学方法已表明驱动蛋白超家族蛋白(KIF)在细胞内运输中起着重要作用,并表明它们对于细胞形态发生,功能和存活至关重要。 KIF不仅转运各种膜细胞器,蛋白质复合物和mRNA,以维持基本的细胞活动,而且还在生命基本机制中发挥重要作用,例如脑部连线,高级脑功能(例如记忆力,学习能力和活动依赖性)神经元在大脑发育过程中的存活,并用于确定重要的发育过程,例如左右不对称形成和抑制肿瘤发生。越来越多的数据揭示了涉及脚手架或衔接蛋白复合物的货物识别的分子机制。分子内折叠和磷酸化也调节运动蛋白的结合活性。使用分子生物物理学,低温电子显微镜和X射线晶体学的新技术已经检测到了运动蛋白的结构变化,并与ATP水解循环同步,从而导致了单体和二聚体电机沿微管进行过程性运动的独立模型的发展。

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