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首页> 外文期刊>Journal of Physics. Condensed Matter >Biophysics of membrane curvature remodeling at molecular and mesoscopic lengthscales
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Biophysics of membrane curvature remodeling at molecular and mesoscopic lengthscales

机译:分子和介观型卷材卷材重塑的生物物理学

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At the micron scale, where cell organelles display an amazing complexity in their shape and organization, the physical properties of a biological membrane can be better-understood using continuum models subject to thermal (stochastic) undulations. Yet, the chief orchestrators of these complex and intriguing shapes are a specialized class of membrane associating often peripheral proteins called curvature remodeling proteins (CRPs) that operate at the molecular level through specific protein-lipid interactions. We review multiscale methodologies to model these systems at the molecular as well as at the mesoscopic and cellular scales, and also present a free energy perspective of membrane remodeling through the organization and assembly of CRPs. We discuss the morphological space of nearly planar to highly curved membranes, methods to include thermal fluctuations, and review studies that model such proteins as curvature fields to describe the emergent curved morphologies. We also discuss several mesoscale models applied to a variety of cellular processes, where the phenomenological parameters (such as curvature field strength) are often mapped to models of real systems based on molecular simulations. Much insight can be gained from the calculation of free energies of membranes states with protein fields, which enable accurate mapping of the state and parameter values at which the membrane undergoes morphological transformations such as vesiculation or tubulation. By tuning the strength, anisotropy, and spatial organization of the curvature-field, one can generate a rich array of membrane morphologies that are highly relevant to shapes of several cellular organelles. We review applications of these models to budding of vesicles commonly seen in cellular signaling and trafficking processes such as clathrin mediated endocytosis, sorting by the ESCRT protein complexes, and cellular exocytosis regulated by the exocyst complex. We discuss future prospects where such models c
机译:在微米尺度,其中的细胞器在它们的形状和组织显示一个惊人的复杂性,生物膜的物理性质可以更好地理解的利用连续模型经受热(随机)起伏。然而,这些复杂的和有趣的形状的主要协调器是一个专门的类膜的缔合,在通过特定的蛋白 - 脂质相互作用的分子水平上进行操作经常周蛋白称为曲率重塑蛋白(的CRP)。我们回顾了多尺度方法,以这些系统在分子,以及在中观和细胞尺度模型,也存在通过组织和组装的CRP重塑膜的自由能的角度。我们讨论了近平面到高度弯曲的膜的形态空间,方法包括热波动,和审查研究,模型等蛋白质曲率字段来描述新兴弯曲形态。我们还讨论适用于各种细胞过程,其中,所述现象的参数(如曲率场强度)通常映射到基于分子模拟真实系统的模型的几个尺度模式。很大的启示可以从与蛋白质字段,其中能够在所述膜经历形状上变换,如囊泡或制管的状态和参数值的准确映射膜状态的自由能的计算来获得。通过调整强度,各向异性,曲率场的空间组织,可以产生丰富的膜的形态是对几个细胞器的形状高度相关的阵列。我们回顾这些模型的应用程序在细胞信号常见的囊泡的萌芽和贩运过程,如网格蛋白介导的内吞作用,由ESCRT蛋白复合物排序,并通过exocyst复杂调节的细胞胞吐。我们讨论了未来的发展前景,其中这种型号C

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