Pattern formation by curvature-inducing proteins on spherical membranes

被引:9
作者
Agudo-Canalejo, Jaime [1 ,2 ,3 ]
Golestanian, Ramin [2 ,4 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Theory & Biosyst Dept, D-14424 Potsdam, Germany
[2] Univ Oxford, Rudolf Peierls Ctr Theoret Phys, Oxford OX1 3NP, England
[3] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[4] Max Planck Inst Phys Komplexer Syst, Nothnitzer Str 38, D-01187 Dresden, Germany
基金
美国国家科学基金会;
关键词
bacterial cell division; membrane elasticity; protein organisation; FLUCTUATION-INDUCED INTERACTIONS; LIPID RAFTS; PLASMA-MEMBRANE; CELL POLARITY; VESICLES; DIVISION; ORGANIZATION; MECHANISMS; TENSION; MODELS;
D O I
10.1088/1367-2630/aa983c
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Spatial organisation is a hallmark of all living cells, and recreating it in model systems is a necessary step in the creation of synthetic cells. It is therefore of both fundamental and practical interest to better understand the basic mechanisms underlying spatial organisation in cells. In this work, we use a continuum model of membrane and protein dynamics to study the behaviour of curvature-inducing proteins on membranes of spherical shape, such as living cells or lipid vesicles. We show that the interplay between curvature energy, entropic forces, and the geometric constraints on the membrane can result in the formation of patterns of highly-curved/protein-rich and weakly-curved/protein-poor domains on the membrane. The spontaneous formation of such patterns can be triggered either by an increase in the average density of curvature-inducing proteins, or by a relaxation of the geometric constraints on the membrane imposed by the membrane tension or by the tethering of the membrane to a rigid cell wall or cortex. These parameters can also be tuned to select the size and number of the protein-rich domains that arise upon pattern formation. The very general mechanism presented here could be related to protein self-organisation in many biological processes, ranging from (proto)cell division to the formation of membrane rafts.
引用
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页数:13
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共 45 条
[1]   Uniform and Janus-like nanoparticles in contact with vesicles: energy landscapes and curvature-induced forces [J].
Agudo-Canalejo, Jaime ;
Lipowsky, Reinhard .
SOFT MATTER, 2017, 13 (11) :2155-2173
[2]   Model for Probing Membrane-Cortex Adhesion by Micropipette Aspiration and Fluctuation Spectroscopy [J].
Alert, Ricard ;
Casademunt, Jaume ;
Brugues, Jan ;
Sens, Pierre .
BIOPHYSICAL JOURNAL, 2015, 108 (08) :1878-1886
[3]   Cytokinesis: Placing and making the final cut [J].
Barr, Francis A. ;
Gruneberg, Ulrike .
CELL, 2007, 131 (05) :847-860
[4]   A polymeric protein anchors the chromosomal origin/ParB complex at a bacterial cell pole [J].
Bowman, Grant R. ;
Comolli, Luis R. ;
Zhu, Jian ;
Eckart, Michael ;
Koenig, Marcelle ;
Downing, Kenneth H. ;
Moerner, W. E. ;
Earnest, Thomas ;
Shapiro, Lucy .
CELL, 2008, 134 (06) :945-955
[5]   HYDRODYNAMICS AND DYNAMIC FLUCTUATIONS OF FLUID MEMBRANES [J].
CAI, WC ;
LUBENSKY, TC .
PHYSICAL REVIEW E, 1995, 52 (04) :4251-4266
[6]   A practical guide to giant vesicles. Probing the membrane nanoregime via optical microscopy [J].
Dimova, Rumiana ;
Aranda, Said ;
Bezlyepkina, Natalya ;
Nikolov, Vesselin ;
Riske, Karin A. ;
Lipowsky, Reinhard .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2006, 18 (28) :S1151-S1176
[7]   Origins of cell polarity [J].
Drubin, DG ;
Nelson, WJ .
CELL, 1996, 84 (03) :335-344
[8]   A self-associating protein critical for chromosome attachment, division, and polar organization in Caulobacter [J].
Ebersbach, Gitte ;
Briegel, Ariane ;
Jensen, Grant J. ;
Jacobs-Wagner, Christine .
CELL, 2008, 134 (06) :956-968
[9]   Supramolecular structure in the membrane of Staphylococcus aureus [J].
Garcia-Lara, Jorge ;
Weihs, Felix ;
Ma, Xing ;
Walker, Lucas ;
Chaudhuri, Roy R. ;
Kasturiarachchi, Jagath ;
Crossley, Howard ;
Golestanian, Ramin ;
Foster, Simon J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (51) :15725-15730
[10]   Cleavage furrow positioning [J].
Glotzer, M .
JOURNAL OF CELL BIOLOGY, 2004, 164 (03) :347-351