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具有共存的液态有序相和液态无序相行为的生物膜中的优先蛋白分配:潜在的设计原则。

Preferential Protein Partitioning in Biological Membrane with Coexisting Liquid Ordered and Liquid Disordered Phase Behavior: Underlying Design Principles.

机构信息

Molecular Biophysics Unit, Indian Institute of Science, Bangalore, Karnataka, 560012, India.

出版信息

J Membr Biol. 2020 Dec;253(6):551-562. doi: 10.1007/s00232-020-00150-1. Epub 2020 Nov 10.

Abstract

Several studies now show that certain proteins exhibit selective preference toward liquid ordered (L[Formula: see text]) or toward liquid disordered (L[Formula: see text]) regions of the heterogeneous membrane and some of them have preference for the L[Formula: see text]-L[Formula: see text] interface. Spatially heterogenous organization of lipids, enriched in specific protein molecules, function as platforms for signaling and are involved in several other physiologically critical functions. In this review, we collate together some of the experimental observations of cases where proteins preferentially segregate into different phases and highlight the importance of these preferential localization in terms of underlying functions. We also try to understand the structural features and chemical makeup of the membrane-interacting motifs of these proteins. Finally, we put forth some preliminary analysis on class I viral fusion proteins, some of which are known to partition at the L[Formula: see text]-L[Formula: see text] interface, and through them we try to understand the evolutionary design principles of phase segregating proteins. Put together, this review summarizes the existing studies on preferential partitioning of proteins into different membrane phases while emphasizing the need to understand the molecular design-level features that can help us "engineer" functionally rich peptides and proteins with a programmed membrane partitioning.

摘要

目前有几项研究表明,某些蛋白质对异质膜中的有序液体(Ld)或无序液体(Lo)区域具有选择性偏好,其中一些蛋白质对 Ld-Lo 界面具有偏好。脂质的空间异质组织富含特定的蛋白质分子,作为信号转导的平台,并参与其他几种生理关键功能。在这篇综述中,我们汇集了一些实验观察结果,这些结果表明蛋白质优先分离到不同的相中,并强调了这些优先定位在潜在功能方面的重要性。我们还试图了解这些蛋白质的膜相互作用基序的结构特征和化学组成。最后,我们对 I 类病毒融合蛋白进行了一些初步分析,其中一些已知在 Ld-Lo 界面处分配,通过它们,我们试图了解相分离蛋白质的进化设计原则。综上所述,本综述总结了目前关于蛋白质优先分配到不同膜相的研究,同时强调需要了解分子设计层面的特征,这些特征可以帮助我们“设计”具有编程膜分配功能的富含肽和蛋白质。

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