Literature DB >> 8312492

Pattern formation in icosahedral virus capsids: the papova viruses and Nudaurelia capensis beta virus.

C J Marzec1, L A Day.   

Abstract

The capsids of the spherical viruses all show underlying icosahedral symmetry, yet they differ markedly in capsomere shape and in capsomere position and orientation. The capsid patterns presented by the capsomere shapes, positions, and orientations of three viruses (papilloma, SV40, and N beta V) have been generated dynamically through a bottom-up procedure which provides a basis for understanding the patterns. A capsomere shape is represented in two-dimensional cross-section by a mass or charge density on the surface of a sphere, given by an expansion in spherical harmonics, and referred to herein as a morphological unit (MU). A capsid pattern is represented by an icosahedrally symmetrical superposition of such densities, determined by the positions and orientations of its MUs on the spherical surface. The fitness of an arrangement of MUs is measured by an interaction integral through which all capsid elements interact with each other via an arbitrary function of distance. A capsid pattern is generated by allowing the correct number of approximately shaped MUs to move dynamically on the sphere, positioning themselves until an extremum of the fitness function is attained. The resulting patterns are largely independent of the details of both the capsomere representation and the interaction function; thus the patterns produced are generic. The simplest useful fitness function is sigma 2, the average square of the mass (or charge) density, a minimum of which corresponds to a "uniformly spaced" MU distribution; to good approximation, the electrostatic free energy of charged capsomeres, calculated from the linearized Poisson-Boltzmann equation, is proportional to sigma 2. With disks as MUs, the model generates the coordinated lattices familiar from the quasi-equivalence theory, indexed by triangulation numbers. Using fivefold MUs, the model generates the patterns observed at different radii within the T = 7 capsid of papilloma and at the surface of SV40; threefold MUs give the T = 4 pattern of Nudaurelia capensis beta virus. In all cases examined so far, the MU orientations are correctly found.

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Year:  1993        PMID: 8312492      PMCID: PMC1225998          DOI: 10.1016/S0006-3495(93)81313-4

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  22 in total

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Authors:  D L CASPAR; A KLUG
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1962

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Authors:  T S Baker; J Drak; M Bina
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Journal:  J Mol Biol       Date:  1988-08-20       Impact factor: 5.469

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Journal:  J Mol Biol       Date:  1979-06-15       Impact factor: 5.469

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Journal:  Ultramicroscopy       Date:  1988       Impact factor: 2.689

6.  Structure of tomato busy stunt virus IV. The virus particle at 2.9 A resolution.

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Journal:  J Mol Biol       Date:  1983-11-25       Impact factor: 5.469

7.  Structure and inherent properties of the bacteriophage lambda head shell. IV. Small-head mutants.

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Journal:  J Mol Biol       Date:  1983-12-15       Impact factor: 5.469

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Journal:  J Mol Biol       Date:  1982-07-25       Impact factor: 5.469

9.  The capsid of small papova viruses contains 72 pentameric capsomeres: direct evidence from cryo-electron-microscopy of simian virus 40.

Authors:  T S Baker; J Drak; M Bina
Journal:  Biophys J       Date:  1989-02       Impact factor: 4.033

10.  The structure of the adenovirus capsid. II. The packing symmetry of hexon and its implications for viral architecture.

Authors:  R M Burnett
Journal:  J Mol Biol       Date:  1985-09-05       Impact factor: 5.469

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  10 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-14       Impact factor: 11.205

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Authors:  D M Belnap; N H Olson; N M Cladel; W W Newcomb; J C Brown; J W Kreider; N D Christensen; T S Baker
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Authors:  C J Marzec; L A Day
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5.  Local rules simulation of the kinetics of virus capsid self-assembly.

Authors:  R Schwartz; P W Shor; P E Prevelige; B Berger
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

6.  Electrostatics-Driven Inflation of Elastic Icosahedral Shells as a Model for Swelling of Viruses.

Authors:  Anže Lošdorfer Božič; Antonio Šiber
Journal:  Biophys J       Date:  2018-08-07       Impact factor: 4.033

7.  How simple can a model of an empty viral capsid be? Charge distributions in viral capsids.

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8.  Pentagon packing models for "all-pentamer" virus structures.

Authors:  T Tarnai; Z Gáspár; L Szalai
Journal:  Biophys J       Date:  1995-08       Impact factor: 4.033

9.  Organized assemblies of colloids formed at the poles of micrometer-sized droplets of liquid crystal.

Authors:  Xiaoguang Wang; Daniel S Miller; Juan J de Pablo; Nicholas L Abbott
Journal:  Soft Matter       Date:  2014-11-28       Impact factor: 3.679

10.  Cleavage and Structural Transitions during Maturation of Staphylococcus aureus Bacteriophage 80α and SaPI1 Capsids.

Authors:  James L Kizziah; Keith A Manning; Altaira D Dearborn; Erin A Wall; Laura Klenow; Rosanne L L Hill; Michael S Spilman; Scott M Stagg; Gail E Christie; Terje Dokland
Journal:  Viruses       Date:  2017-12-16       Impact factor: 5.048

  10 in total

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