Cholesterol stabilizes recombinant exocytic fusion pores by altering membrane bending rigidity

Author(s):  
Lanxi Wu ◽  
Kevin C. Courtney ◽  
Edwin R. Chapman
2012 ◽  
Vol 102 (3) ◽  
pp. 413a
Author(s):  
George Khelashvili ◽  
Michael Rappolt ◽  
See-Wing Chiu ◽  
Georg Pabst ◽  
Daniel Harries

2019 ◽  
Author(s):  
Feng Xue ◽  
Charles D. Cox ◽  
Navid Bavi ◽  
Paul R Rohde ◽  
Yoshitaka Nakayama ◽  
...  

AbstractProkaryotic mechanosensitive (MS) channels have an intimate relationship with membrane lipids. Membrane lipids may influence channel activity by directly interacting with bacterial MS channels or by influencing the global properties of the membrane such as area stretch and bending moduli. Previous work has implicated membrane stiffness as a key determinant of the mechanosensitivity of E. coli (Ec)MscS. Here we systematically tested this hypothesis using patch fluorometry of azolectin liposomes doped with lipids of increasing area stretch moduli. Increasing DOPE content of azolectin liposomes causes a rightward shift in the tension response curve of EcMscS. These rightward shifts are further magnified by the addition of stiffer forms of PE such as the branched chain lipid DPhPE and the fully saturated lipid DSPE. Furthermore, a comparison of the branched chain lipid DPhPC to the stiffer DPhPE showed a rightward shift in the tension response curve in the presence of the stiffer DPhPE. We show that these changes are not due to changes in membrane bending rigidity as the tension threshold of EcMscS in membranes doped with PC18:1 and PC18:3 are the same, despite a two-fold difference in their bending rigidity. We also show that after prolonged pressure application sudden removal of force in softer membranes causes a rebound reactivation of EcMscS and we discuss the relevance of this phenomenon to bacterial osmoregulation. Collectively, our data demonstrate that membrane stiffness is a key determinant of the mechanosensitivity of EcMscS.


2007 ◽  
Vol 18 (08) ◽  
pp. 1277-1291 ◽  
Author(s):  
Y. SUI ◽  
Y. T. CHEW ◽  
P. ROY ◽  
H. T. LOW

The transient deformation of liquid capsules enclosed by elastic membranes in two-dimensional extensional flow is studied numerically, using an improved immersed boundary-lattice Boltzmann method. The purpose of the present study is to investigate the effect of interfacial bending stiffness on the deformation of such capsules, under the subcritical elasticity capillary number conditions. The present model can simulate flow-induced deformation of capsules with arbitrary resting shapes (concerning the in-plane tension) and bending-free configurations. The deformation of capsules with initially circular, elliptical, and biconcave resting shapes was investigated in the present study; the capsules' bending-free configurations were considered as either circular shapes or their initially resting shapes. The results show that for capsules with bending-free configuration as circles, membrane bending rigidity has significant rounding effect on the steady deformed profiles. For elliptical and biconcave capsules with resting shapes as the bending-free configurations, it is found that with the bending stiffness increasing, the capsules' steady shapes are more akin to their initial shapes.


2007 ◽  
Vol 98 (25) ◽  
Author(s):  
Erol Kurtisovski ◽  
Nicolas Taulier ◽  
Raymond Ober ◽  
Marcel Waks ◽  
Wladimir Urbach

Langmuir ◽  
2004 ◽  
Vol 20 (3) ◽  
pp. 540-543 ◽  
Author(s):  
H. Bermúdez ◽  
D. A. Hammer ◽  
D. E. Discher

2011 ◽  
Vol 440 (2) ◽  
pp. 185-193 ◽  
Author(s):  
Jean-Philippe Richard ◽  
Evgenia Leikina ◽  
Ralf Langen ◽  
William Mike Henne ◽  
Margarita Popova ◽  
...  

Cell-to-cell fusion plays an important role in normal physiology and in different pathological conditions. Early fusion stages mediated by specialized proteins and yielding fusion pores are followed by a pore expansion stage that is dependent on cell metabolism and yet unidentified machinery. Because of a similarity of membrane bending in the fusion pore rim and in highly curved intracellular membrane compartments, in the present study we explored whether changes in the activity of the proteins that generate these compartments affect cell fusion initiated by protein fusogens of influenza virus and baculovirus. We raised the intracellular concentration of curvature-generating proteins in cells by either expressing or microinjecting the ENTH (epsin N-terminal homology) domain of epsin or by expressing the GRAF1 (GTPase regulator associated with focal adhesion kinase 1) BAR (Bin/amphiphysin/Rvs) domain or the FCHo2 (FCH domain-only protein 2) F-BAR domain. Each of these treatments promoted syncytium formation. Cell fusion extents were also influenced by treatments targeting the function of another curvature-generating protein, dynamin. Cell-membrane-permeant inhibitors of dynamin GTPase blocked expansion of fusion pores and dominant-negative mutants of dynamin influenced the syncytium formation extents. We also report that syncytium formation is inhibited by reagents lowering the content and accessibility of PtdIns(4,5)P2, an important regulator of intracellular membrane remodelling. Our findings indicate that fusion pore expansion at late stages of cell-to-cell fusion is mediated, directly or indirectly, by intracellular membrane-shaping proteins.


2014 ◽  
Vol 11 (100) ◽  
pp. 20140769 ◽  
Author(s):  
Seyed Mahmoud Hashemi ◽  
Pierre Sens ◽  
Farshid Mohammad-Rafiee

The adsorption of external objects to the cell membrane often triggers cellular responses involving large deformations. In phagocytosis, upon contact with the target, the cell creates large extensions that wrap around the target and ultimately lead to its engulfment. Although active force generation, in particular by actin polymerization, is required for completion of this process, the elastic deformation of the cell membrane upon adhesion to an external object might play an important part in its initiation. In this paper, the elastic deformation of a bilayer owing to the binding of a cylindrical object is studied, taking into account the membrane bending rigidity and the surface tension, the membrane adhesion to both the external target and inner cytoskeleton. The problem is studied within the framework of the Helfrich–Hamiltonian and using force balance relations and the proper boundary conditions that are related to the adhesion energy coefficients. It is shown that membrane wrapping around the target may be a continuous or abrupt transition upon increasing the target binding energy, depending on the value of the parameter. The degree of wrapping and the shape of the membrane in the vicinity of the object are computed numerically, and analytical expressions are given for the boundaries separating the different wrapping regimes in the parameter space.


Sign in / Sign up

Export Citation Format

Share Document