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Open AccessJournal ArticleDOI

Thermodynamics and Mechanics of Membrane Curvature Generation and Sensing by Proteins and Lipids

TLDR
The present review first provides an overview of important classes of membrane proteins for which function is coupled to membrane curvature, and surveys several mechanisms that are assumed to underlie membranes curvature sensing and generation.
Abstract
Research investigating lipid membrane curvature generation and sensing is a rapidly developing frontier in membrane physical chemistry and biophysics. The fast recent progress is based on the discovery of a plethora of proteins involved in coupling membrane shape to cellular membrane function, the design of new quantitative experimental techniques to study aspects of membrane curvature, and the development of analytical theories and simulation techniques that allow a mechanistic interpretation of quantitative measurements. The present review first provides an overview of important classes of membrane proteins for which function is coupled to membrane curvature. We then survey several mechanisms that are assumed to underlie membrane curvature sensing and generation. Finally, we discuss relatively simple thermodynamic/mechanical models that allow quantitative interpretation of experimental observations.

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Dynamin, a membrane-remodelling GTPase

TL;DR: Understanding of the mechanisms by which dynamin acts, its essential roles in cell physiology and the specific function of different dynamin isoforms are improved, highlighting specific contributions of this GTPase to the physiology of different tissues.
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The Fluid—Mosaic Model of Membrane Structure: Still relevant to understanding the structure, function and dynamics of biological membranes after more than 40 years

TL;DR: In updated versions of the model more emphasis has been placed on the mosaic nature of the macrostructure of cellular membranes where many protein and lipid components are limited in their rotational and lateral motilities in the membrane plane, especially in their natural states.
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Membrane bending by protein-protein crowding

TL;DR: A third general mechanism for bending fluid cellular membranes: protein–protein crowding is proposed, and it is found that even proteins unrelated to membrane curvature, such as green fluorescent protein (GFP), can bend membranes when sufficiently concentrated.
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Computational Modeling of Realistic Cell Membranes

TL;DR: The state of the art in the field of realistic membrane simulations is reviewed and the current limitations and challenges ahead are discussed.
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Recent developments in the field of bending rigidity measurements on membranes.

TL;DR: The effect on the bending rigidity of membranes as a function of membrane composition, presence of various inclusions in the bilayer and molecules and ions in the bathing solutions is summarized.
References
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Journal ArticleDOI

Elastic Properties of Lipid Bilayers: Theory and Possible Experiments

TL;DR: A theory of the elasticity of lipid bilayers is proposed and it is argued that in the case of vesicles (= closed bilayer films) the only elasticity controlling nonspherical shapes is that of curvature.
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Membrane curvature and mechanisms of dynamic cell membrane remodelling

TL;DR: Membrane curvature is no longer seen as a passive consequence of cellular activity but an active means to create membrane domains and to organize centres for membrane trafficking.
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BAR domains as sensors of membrane curvature: the amphiphysin BAR structure

TL;DR: The structure of the Drosophila amphiphysin BAR domain is solved and it is predicted that BAR domains are in many protein families, including sorting nexins, centaurins, and oligophrenins.
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Configurations of fluid membranes and vesicles

TL;DR: In this article, the authors describe the systematic physical theory developed to understand the static and dynamic aspects of membrane and vesicle configurations, and the preferred shapes arise from a competition between curvature energy which derives from the bending elasticity of the membrane, geometrical constraints such as fixed surface area and fixed enclosed volume, and a signature of the bilayer aspect.
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