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Physique théorique des systèmes biologiques
(24) Production(s) de l'année 2016
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Multipole analysis of the strain-mediated coupling between proteins adsorbed at tubular lipid membrane surface.
Auteur(s): Golushko I., Rochal S B, Lorman V.
(Article) Publié:
European Physical Journal E, vol. 39 p.128 (2016)
Ref HAL: hal-01529981_v1
PMID 28000047
DOI: 10.1140/epje/i2016-16128-0
WoS: 000397028700001
Exporter : BibTex | endNote
Résumé: The tubular lipid membranes (TLMs) pulled out from vesicles are often used in in vitro studies of the interactions between curvature-inducing proteins and highly curved membranes. The protein molecules adsorbed at the membrane surface deform the TLM and couple with each other due to the induced strain. Here we propose an approach which models the single curvature-inducing protein action on the lipid bilayer by the multipole, the superposition of the point forces applied to the membrane in the region of the protein adsorption. We show that to be localized in the area of the protein size at the TLM surface, the force multipoles satisfying the mechanical equilibrium conditions should be composed of three or more point forces. The protein coupling energy mediated by the membrane strain is studied in detail. In the region of the tubular membrane stability the maximal distance between two neighboring interacting protein-induced force multipoles is estimated to be of the order of the TLM cross section perimeter. In the vicinity of the TLM instability in the region of the vanishing stretching force applied to the TLM, the interaction radius increases drastically. The high affinity of the single curvature-inducing protein molecule to the regions in the vicinity of the TLM ends is explained and related to the boundary conditions in the experimental set-ups. The reasons for the aggregate formation on the membrane surface are also discussed.
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Hidden symmetry of small spherical viruses and organization principles in "anomalous" and double-shelled capsid nanoassemblies.
Auteur(s): Rochal S.B., Konevtsova O., Myasnikova A.E., Lorman V.
(Article) Publié:
Nanoscale, vol. 8 p.16976-16988 (2016)
Ref HAL: hal-01374628_v1
PMID 27714069
DOI: 10.1039/c6nr04930c
WoS: 000385383100021
Exporter : BibTex | endNote
13 Citations
Résumé: We propose the principles of structural organization in spherical nanoassemblies with icosahedral symmetry constituted by asymmetric protein molecules. The approach modifies the paradigmatic geometrical Caspar and Klug (CK) model of icosahedral viral capsids and demonstrates the common origin of both the "anomalous" and conventional capsid structures. In contrast to all previous models of "anomalous" viral capsids the proposed modified model conserves the basic structural principles of the CK approach and reveals the common hidden symmetry underlying all small viral shells. We demonstrate the common genesis of the "anomalous" and conventional capsids and explain their structures in the same frame. The organization principles are derived from the group theory analysis of the positional order on the spherical surface. The relationship between the modified CK geometrical model and the theory of two-dimensional spherical crystallization is discussed. We also apply the proposed approach to complex double-shelled capsids and capsids with protruding knob-like proteins. The introduced notion of commensurability for the concentric nanoshells explains the peculiarities of their organization and helps to predict analogous, but yet undiscovered, double-shelled viral capsid nanostructures.
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A variational approach to the liquid-vapor phase transition for hardcore ions in the bulk and in nanopores.
Auteur(s): Loubet Bastien, Manghi Manoel, Palmeri J.
(Article) Publié:
The Journal Of Chemical Physics, vol. 145 p.044107 (2016)
Texte intégral en Openaccess :
Ref HAL: hal-01360415_v1
Ref Arxiv: 1604.05532
DOI: 10.1063/1.4959034
WoS: 000381679800009
Ref. & Cit.: NASA ADS
Exporter : BibTex | endNote
7 Citations
Résumé: We employ a field-theoretical variational approach to study the behavior of ionic solutions in the grand canonical ensemble. To describe properly the hardcore interactions between ions, we use a cutoff in Fourier space for the electrostatic contribution of the grand potential and the Carnahan-Starling equation of state with a modified chemical potential for the pressure one. We first calibrate our method by comparing its predictions at room temperature with Monte Carlo results for excess chemical potential and energy. We then validate our approach in the bulk phase by describing the classical “ionic liquid-vapor” phase transition induced by ionic correlations at low temperature, before applying it to electrolytes at room temperature confined to nanopores embedded in a low dielectric medium and coupled to an external reservoir of ions. The ionic concentration in the nanopore is then correctly described from very low bulk concentrations, where dielectric exclusion shifts the transition up to room temperature for sufficiently tight nanopores, to high concentrations where hardcore interactions dominate which, as expected, modify only slightly this ionic “capillary evaporation.”
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Foci of cyclin A2 interact with actin and RhoA in mitosis
Auteur(s): Loukil Abdelhalim, Izard Fanny, Georgieva Mariya, Mashayekhan Shaereh, Blanchard Jean-Marie, Parmeggiani A., Peter Marion
(Article) Publié:
Scientific Reports, vol. 6 p.27215 (2016)
Texte intégral en Openaccess :
Ref HAL: hal-01345990_v1
DOI: 10.1038/srep27215
WoS: WOS:000377338000001
Exporter : BibTex | endNote
Résumé: Cyclin A2 is a key player in the regulation of the cell cycle. Its degradation in mid-mitosis depends primarily on the ubiquitin-proteasome system (UPS), while autophagy also contributes. However, a fraction of cyclin A2 persists beyond metaphase. In this work, we focus on cyclin A2-rich foci detected in mitosis by high resolution imaging and analyse their movements. We demonstrate that cyclin A2 interacts with actin and RhoA during mitosis, and that cyclin A2 depletion induces a dramatic decrease in active RhoA in mitosis. Our data suggest cyclin A2 participation in RhoA activation in late mitosis.
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Theory of morphological transformation of viral capsid shell during the maturation process in the HK97 bacteriophage and similar viruses.
Auteur(s): Konevtsova O., Lorman V., Rochal S.B.
(Article) Publié:
Physical Review E: Statistical, Nonlinear, And Soft Matter Physics, vol. 93 p.052412 (2016)
Texte intégral en Openaccess :
Ref HAL: hal-01319073_v1
PMID 27300929
DOI: 10.1103/PhysRevE.93.052412
WoS: 000376262700007
Exporter : BibTex | endNote
4 Citations
Résumé: We consider the symmetry and physical origin of collective displacement modes playing a crucial role in the morphological transformation during the maturation of the HK97 bacteriophage and similar viruses. It is shown that the experimentally observed hexamer deformation and pentamer twist in the HK97 procapsid correspond to the simplest irreducible shear strain mode of a spherical shell. We also show that the icosahedral faceting of the bacteriophage capsid shell is driven by the simplest irreducible radial displacement field. The shear field has the rotational icosahedral symmetry group I while the radial field has the full icosahedral symmetry I_{h}. This difference makes their actions independent. The radial field sign discriminates between the icosahedral and the dodecahedral shapes of the faceted capsid shell, thus making the approach relevant not only for the HK97-like viruses but also for the parvovirus family. In the frame of the Landau-Ginzburg formalism we propose a simple phenomenological model valid for the first reversible step of the HK97 maturation process. The calculated phase diagram illustrates the discontinuous character of the virus shape transformation. The characteristics of the virus shell faceting and expansion obtained in the in vitro and in vivo experiments are related to the decrease in the capsid shell thickness and to the increase of the internal capsid pressure.
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Principles of formation of viral capsids with double protein shells
Auteur(s): Konevtsova O., Rochal S.B., Lorman V.
Conference: 50th Winter School on Condensed Matter Physics (Saint Petersbourg, RU, 2016-03-14)
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Physics of virus self-assembly and virus-like biological nanoparticles
Auteur(s): Lorman V., Rochal S.b.
Conference: 50th Winter School on Condensed Matter Physics (Saint Petersbourg, RU, 2016-03-14)
Résumé: Physics of virus self-assembly and virus-like biological nanoparticles
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