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蛋白质-磷脂相互作用基序:聚焦于磷脂酸。

Protein⁻Phospholipid Interaction Motifs: A Focus on Phosphatidic Acid.

机构信息

Institut des Neurosciences Cellulaires et Intégratives, CNRS UPR3212 and Université de Strasbourg, 67000 Strasbourg, France.

出版信息

Biomolecules. 2018 Apr 23;8(2):20. doi: 10.3390/biom8020020.

Abstract

Cellular membranes are composed of thousands of different lipids usually maintained within a narrow range of concentrations. In addition to their well-known structural and metabolic roles, signaling functions for many lipids have also emerged over the last two decades. The latter largely depend on the ability of particular classes of lipids to interact specifically with a great variety of proteins and to regulate their localization and activity. Among these lipids, phosphatidic acid (PA) plays a unique role in a large repertoire of cellular activities, most likely in relation to its unique biophysical properties. However, until recently, only incomplete information was available to model the interaction between PA and its protein partners. The development of new liposome-based assays as well as molecular dynamic simulation are now providing novel information. We will review the different factors that have shown to modulate the capacity of PA to interact with specific domains in target proteins.

摘要

细胞膜由数千种不同的脂质组成,通常维持在狭窄的浓度范围内。除了众所周知的结构和代谢作用外,过去二十年中还出现了许多脂质的信号功能。后者在很大程度上取决于特定脂质类别的能力,这些脂质能够与各种蛋白质特异性相互作用,并调节其定位和活性。在这些脂质中,磷脂酸 (PA) 在大量细胞活动中发挥独特的作用,这很可能与其独特的物理化学性质有关。然而,直到最近,用于模拟 PA 与其蛋白质伴侣相互作用的信息才不完全。基于脂质体的新测定方法以及分子动力学模拟的发展现在提供了新的信息。我们将回顾已显示可调节 PA 与靶蛋白中特定结构域相互作用能力的不同因素。

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