ライフサイエンスコーパス: icosahedral

1 pparent hexameric symmetry positioned on the icosahedral 2-fold axes.

2 psid only displays 30 spikes, located on the icosahedral 2-fold axes.

3 a second site, at least 50 A distant, at the icosahedral 2-fold axes.

4 positioned the betaA strand region under the icosahedral 2-fold axis rather than antiparallel to the

5 while tilting of the P domain away from the icosahedral 2-fold axis was seen in the CC dimers.

6 ii) the exterior capsid surface close to the icosahedral 2-fold depression.

7 teractions act as "molecular staples" at the icosahedral 2-fold symmetry axis and significantly contr

8 her parvoviruses, such as depressions at the icosahedral 2-fold symmetry axis and surrounding the 5-f

9 The spikes on the icosahedral 3-fold axes and those in general positions a

10 et at the base of the protrusions around the icosahedral 3-fold axes of symmetry.

11 tributing to the protrusions surrounding the icosahedral 3-fold axes of the AAVs, is shorter in AAV5,

12 Steric hindrance around the icosahedral 3-fold axes prevents binding of a Fab to the

13 the N termini of the three C subunits at the icosahedral 3-fold axes.

14 h destabilization of the beta-annulus at the icosahedral 3-fold axes.

15 t the base of capsid protrusions surrounding icosahedral 3-fold axes.

16 a epitope to the protrusions surrounding the icosahedral 3-fold axis and the ADK1b and ADK5a epitopes

17 the interior surface of the capsid under the icosahedral 3-fold axis near ordered nucleic acid densit

18 hese residues are located at or close to the icosahedral 3-fold axis of the capsid, thereby identifyi

19 ons: 12 pentameric turrets positioned on the icosahedral 5-fold axes and 30 turrets with apparent hex

20 ay be attributed to lysine residues near the icosahedral 5-fold axes of symmetry.

21 rs below the coat protein dimers forming the icosahedral 5-fold axes of the capsid.

22 erturb the base of cylinders surrounding the icosahedral 5-fold axes of the virus, and show that thes

23 how that BRV lacks a protruding fiber at its icosahedral 5-fold axes or elsewhere.

24 Large-area icosahedral-AB(13)-type Pt-Pd binary superlattices (BNSL

25 Using a hitherto unexplored template, the icosahedral Ag-In-Yb quasicrystal, and various experimen

26 udy extend our knowledge on the stability of icosahedral AlCuFe at higher temperature and pressure th

27 tability at ambient temperature of synthetic icosahedral AlCuFe up to ~35 GPa, the simultaneous effec

28 n X-ray diffraction experiments on synthetic icosahedral AlCuFe using multianvil device to explore po

29 The icosahedral and asymmetric reconstructions of the virus

30 ng different crystallographic directions for icosahedral and decagonal quasicrystals and (4) what are

31 The Khatyrka meteorite contains both icosahedral and decagonal quasicrystals.

32 plets can be reversibly temperature-tuned to icosahedral and other faceted shapes, hitherto unreporte

33 age lambda, the covalent crosslinking at the icosahedral and quasi threefold axes of HK97 yields a me

34 ulk diffusivities of several near-spherical (icosahedral) and nonspherical (tailed) bacterial viruses

35 Many virus capsids are icosahedral, and assembly is thought to occur by the seq

36 Zika virions are enveloped and icosahedral, and contain a nonsegmented, single-stranded

37 mmetry averaging techniques that exploit the icosahedral architecture seen in many viruses.

38 show that 10 designs spanning three distinct icosahedral architectures form materials closely matchin

39 edral symmetry--tetrahedral, octahedral, and icosahedral--are the 5 Platonic polyhedra, the 13 Archim

40 apsid proteins (VP1 to VP3) adopt an altered icosahedral arrangement to open holes in the capsid at 2

41 kage one full-length RNA genome for every 11 icosahedral assemblies, similar to the best recombinant

42 ious rotavirus particles are triple-layered, icosahedral assemblies.

43 ng the four quasi-equivalent subunits in the icosahedral asymmetric unit.

44 there are four and one-third VP6 trimers per icosahedral asymmetric unit.

45 opy (cryo-EM), showed only four proteins per icosahedral asymmetric unit: a dimer of the major capsid

46 between {111} and {110} facets grown on the icosahedral Au seeds, NCs with icosahedral, icosidodecah

47 of two incomplete (i.e., one vertex missing) icosahedral Au(12) units joined by five thiolate linkage

48 BT)50 structure with the recently discovered icosahedral Au133(p-TBBT)52 nanocluster (where p-TBBT =

49 much larger than the gap (0.9 eV) of the bi-icosahedral [Au38(SCH2CH2Ph)24].

50 e 5-fold and 2-fold but not along the 3-fold icosahedral axes.

51 hydrogen atoms, or hydrides from the stable icosahedral B(12)H(12)(2-) is investigated theoretically

52 We also show that a layer composed of icosahedral B12 is unfavorable on Cu and Ni but unexpect

53 ach can be utilized in other filamentous and icosahedral bacteriophages, and also in other biomolecul

54 ery of a family of at least seven rare earth icosahedral binary quasicrystals, i-R-Cd (R = Gd to Tm,

55 A single B-OH vertex of the icosahedral borane [closo-B(12)(OH)(12)](2-) was derivat

56 Icosahedral boranes, carboranes, and metallacarboranes a

57 Icosahedral boron cluster derivatives have been reviewed

58 iloxane and coordination polymers containing icosahedral boron clusters in the last few decades, whic

59 le model, the extraordinary abundance of the icosahedral C80 cage in EMFs can be easily understood.

60 ne complex containing two boron atoms of the icosahedral cage connected to a single exohedral metal c

61 ks are assembled to build a highly symmetric icosahedral cage.

62 two of the major particle compartments, the icosahedral capsid and the amorphous tegument, has been

63 virus (NomegaV), an insect RNA virus with an icosahedral capsid formed by protein alpha, which underg

64 nd many bacteriophages, is packed inside its icosahedral capsid in liquid-crystalline form, with conc

65 The icosahedral capsid is composed of the major capsid prote

66 he product of gene 58, is assembled onto the icosahedral capsid lattice.

67 ng different positions in a quasi-equivalent icosahedral capsid play different roles in host infectio

68 protein and the major capsid protein into an icosahedral capsid shell.

69 oduced an atomic model for a continuous, T=3 icosahedral capsid shell.

70 icroscopy of this novel phage revealed a T=9 icosahedral capsid structure with the major capsid prote

71 yovirus KZ has a 270-kb genome within a T=27 icosahedral capsid that contains a large, unusual, and s

72 us (HBV) core protein (HBc) assemble into an icosahedral capsid that packages the viral pregenomic RN

73 transcribed and replicated in a specialized icosahedral capsid with a T=1 lattice consisting of 60 a

74 glycans composing the fibers surrounding its icosahedral capsid, including the dideoxyhexose viosamin

75 racteristic particle structure comprising an icosahedral capsid, which contains the DNA genome and is

76 d an internal lipid membrane enclosed in the icosahedral capsid.

77 surface, merging seamlessly to complete the icosahedral capsid.

78 rings at the special five-fold vertex of the icosahedral capsid.

79 f HAstV produced an atomic model for the T=3 icosahedral capsid.

80 ted by the L1 C terminus to constitute a T=7 icosahedral capsid.

81 Viruses build icosahedral capsids of specific size and shape by regula

82 Icosahedral capsids of viruses are lattices of defined g

83 These viruses share structurally related icosahedral capsids that encase the double-stranded DNA

84 tinocytes containing densely packed 36-45-nm icosahedral capsids.

85 nserved number of transcription complexes in icosahedral capsids.

86 virus (RSV) CA-SP to assemble in vitro into icosahedral capsids.

87 sions surrounding the 3-fold axes of the T=1 icosahedral capsids.

88 he major capsid protein, gp23, produced T=13 icosahedral capsids.

89 , supported by computational work, show that icosahedral carboranes can act either as strong electron

90 t that, in contrast to carbon-based ligands, icosahedral carboranes exhibit a significant dichotomy i

91 coordinating moieties, we describe here how icosahedral carboranes-boron-rich clusters-can influence

92 Several representative vertex-differentiated icosahedral closo-boranes were prepared utilizing carbon

93 s for the synthesis of vertex-differentiated icosahedral closo-boranes.

94 eometrical motif where a nonchiral Au(26) bi-icosahedral cluster core is protected by 6 RS-Au-SR and

95 consistent with six-shell cuboctahedral and icosahedral clusters containing ~600 Pd atoms, where 45%

96 r clues to the driving forces underlying the icosahedral clusters that occur in Bergman-type quasicry

97 The stressosome is a multiprotein, 1.8-MDa icosahedral complex that transmits diverse environmental

98 In vitro assembly of icosahedral complexes from independently purified compon

99 mes in E. coli resulted in the production of icosahedral complexes similar to those from the native h

100 24)(SC(2)H(4)Ph)(18) possesses a Pt-centered icosahedral core capped by six Au(2)(SC(2)H(4)Ph)(3) sta

101 on to confirming the theoretically predicted icosahedral-cored cluster, we also find samples with a t

102 We validate that Ag nanocrystals with icosahedral, decahedral, and single-crystal structures a

103 By combining a cell-targetable, icosahedral DNA-nanocapsule loaded with photoresponsive

104 We report a discovery that perfunctionalized icosahedral dodecaborate clusters of the type B12(OCH2Ar

105 ction that probably also occurs in other big icosahedral double jelly-roll viruses such as Adenovirus

106 In most icosahedral double-stranded (ds) DNA viruses, the viral

107 IMPORTANCE Pacmanvirus is a newly discovered icosahedral double-stranded DNA virus that was isolated

108 d of 260 hexagonal units and 13 hexagons per icosahedral face.

109 though elastic theory explains one-component icosahedral faceting, the possibility of buckling into o

110 ab bound only to epitopes located around the icosahedral five-fold vertex of the capsid.

111 he preformed capsid via a pore at one of its icosahedral fivefold axes.

112 small tilt of the core stack relative to the icosahedral fivefold axis and propose that this tilt ass

113 rm bilayers that interact with PhiX174 at an icosahedral fivefold vertex and induce single-stranded (

114 ribution of perforated bilayer vesicles with icosahedral, football, or tennis ball structures.

115 NCs with tetrahedral, cubic, octahedral, and icosahedral geometries have been chemically synthesized,

116 arison with interior 55-metal-atom two-shell icosahedral geometries observed within the multi-shell c

117 apsid of coliphage T5 is organized with T=13 icosahedral geometry and encloses a double-stranded DNA

118 e carbon fullerenes and faceted viruses, the icosahedral Goldberg polyhedra are nearly spherical.

119 e 8 shell electrons are localized at the two icosahedral halves of the metal core.

120 ; they have large genomes packaged within an icosahedral head and a long, contractile tail through wh

121 e shows that each BPP-1 particle has a T = 7 icosahedral head and an unusual tail apparatus consistin

122 r motor assembled at the portal vertex of an icosahedral head.

123 Our results indicate that PVL phages with icosahedral heads, including Phi108PVL and PhiPVL, were

124 L17 and pUL25 on the structural stability of icosahedral herpes simplex virus capsids.

125 grown on the icosahedral Au seeds, NCs with icosahedral, icosidodecahedral, and dodecahedral shapes

126 in the formation of TiLu2C@I(h)-C80 with an icosahedral Ih(7) carbon cage.

127 ese shapes represent a family of Au NCs with icosahedral (Ih) symmetry.

128 , we are able to identify the proportions of icosahedral (Ih), decahedral (Dh), and face-centered cub

129 We used electron cryomicroscopy and icosahedral image analysis to determine the first experi

130 sed transmission electron cryomicroscopy and icosahedral image reconstruction to examine the GLV viri

131 Using electron cryomicroscopy and icosahedral image reconstruction, we determined the viri

132 In all herpesviruses, the capsid is icosahedral in shape, composed of 162 capsomers, and ass

133 .5 A resolution map of the 1,900 A diameter, icosahedral, internally enveloped Paramecium bursaria ch

134 neral features with the previously described icosahedral large DNA viruses, the Pandoraviruses appear

135 fic for the conjugative F-pilus, has a T = 3 icosahedral lattice of coat proteins assembled around it

136 d 89 coat protein dimers arranged in a T = 3 icosahedral lattice.

137 nd gp10 protein subunits that form the T = 7 icosahedral lattice.

138 otein has an HK97 fold arranged into a T = 4 icosahedral lattice.

139 udohexameric capsomers organized on a T = 49 icosahedral lattice.

140 vertex and propagating its growth on a T = 7 icosahedral lattice.

141 The 70-nm-diameter virion is built on a T=28 icosahedral lattice.

142 he rationale of our approach is to establish icosahedral local coordinates to estimate the statistica

143 heory of finite ideal gas reference state to icosahedral local coordinates.

144 We propose a series of icosahedral matryoshka clusters of A@B12@A20 (A = Sn, Pb

145 All of these icosahedral matryoshka clusters, including two previousl

146 r viral genome encapsidation in the tailless icosahedral membrane-containing bacteriophage PRD1.

147 Tectiviridae comprises a group of tailless, icosahedral, membrane-containing bacteriophages that can

148 isolated from a hypersaline environment: an icosahedral, membrane-containing double-stranded DNA vir

149 e rare 8,1,2-closo-MC2B9 isomeric form of an icosahedral metallacarborane have been isolated as unexp

150 These include icosahedral Mimiviruses, amphora-shaped Pandoraviruses,

151 The new icosahedral mineral formed naturally and was discovered

152 dominated by the three-dimensional (3D) B12 icosahedral motifs,4 new forms of elemental boron are co

153 atonic dodecahedral Au NCs can be grown from icosahedral multiply twinned Au seeds.

154 ure revealed are consistent with a distorted icosahedral multiply twinned particle.

155 conditions, we can eliminate completely all icosahedral nanoclusters, which are commonly found under

156 ribes the synthesis of Pt-M (M = Au, Ni, Pd) icosahedral nanocrystals based on the gas reducing agent

157 Among the Pt-M alloy icosahedral nanocrystals generated, Pt(3)Ni had an impre

158 entire transformation process of strained Pt icosahedral nanoparticles (ICNPs) into larger FCC crysta

159 the Picornaviridae family, which consists of icosahedral, nonenveloped, single-stranded RNA viruses.

160 es represent new genera, the podoviruses and icosahedral, nontailed ssDNA phages were exceptional, wi

161 Herpesviruses have an icosahedral nucleocapsid surrounded by an amorphous tegu

162 one, and a systematic, countable infinity of icosahedral ones, one for each Goldberg triangle.

163 etallic compounds and either of face-centred-icosahedral or primitive-icosahedral type, and the posit

164 a high cooling rate; and (ii) competition of icosahedral order against crystal order near the critica

165 molecule condensed by proteins (core) lacks icosahedral order characteristic of the virus protein co

166 he chemical origins of long- and short-range icosahedral order remain mysterious and a subject of deb

167 Our results differ from the T=12 icosahedral organization found for some bunyaviruses.

168 oximately spherical rubella virions lack the icosahedral organization which characterizes Ross River

169 hat, in the presence of those perturbations, icosahedral packing is not the most stable arrangement f

170 protein (VP1) of all caliciviruses forms an icosahedral particle with two principal domains, shell (

171 positive-sense RNA genome packaged in a T=3 icosahedral particle.

172 NA) and is contained within a non-enveloped, icosahedral particle.

173 This assembly process yields T = 1 icosahedral particles comprised of 12 pentamers and one

174 taining double-stranded DNA virus--Salisaeta icosahedral phage 1 (SSIP-1) and its halophilic host bac

175 nal metals expand the stability range of the icosahedral phase and facilitate routine syntheses witho

176 The compositional range of the icosahedral phase is Al68-73Fe11-16Cu10-12Cr1-4Ni1-2 and

177 In the AlPdMn icosahedral phase, above T = 500 degrees C, equilibrium

178 on the examples of i-Ag-In-Yb and i-Al-Cu-Fe icosahedral phases and d-Al-Co-Ni decagonal phase.

179 e experimental results presented address the icosahedral phases in the well explored systems Al-Pd-Mn

180 The chemistry of both the icosahedral phases was characterized by electron micropr

181 Caliciviridae are small icosahedral positive-sense RNA-containing viruses and in

182 single-stranded RNA (ssRNA) segments into an icosahedral procapsid which serves as a compartment for

183 f viral double-stranded DNA (dsDNA) into the icosahedral prohead shell is catalyzed by TerL, a motor

184 can be generalized for all symmetry types of icosahedral protein architectures to monitor protein cag

185 ocapsids, which are computationally designed icosahedral protein assemblies with positively charged i

186 protein-based molecular machines, including icosahedral protein cages that serve as scaffolds, enzym

187 systems to monitor conformational changes in icosahedral protein cages using site-directed spin label

188 tic mottle virus (CCMV) forms highly elastic icosahedral protein capsids that undergo a characteristi

189 embers of the genus Prochlorococcus, contain icosahedral protein microcompartments known as carboxyso

190 of co-assembling, two-component, 120-subunit icosahedral protein nanostructures with molecular weight

191 s of a major capsid protein assemble into an icosahedral protein shell into which the viral genome is

192 lf-assembly pathway of a most simple (T = 1) icosahedral protein shell.

193 is the carboxysome, which is composed of an icosahedral proteinaceous shell encapsulating the key ca

194 ther show that the area-specific activity of icosahedral Pt(3)Ni catalysts was about 50% higher than

195 The Burgers vector of a dislocation in an icosahedral quasicrystal is a 6-dimensional vector, whic

196 We report the first occurrence of an icosahedral quasicrystal with composition Al62.0(8)Cu31.

197 ns in Russia and containing icosahedrite, an icosahedral quasicrystalline phase with composition Al(6

198 Icosahedral quasicrystals (IQCs) are a form of matter th

199 is article the properties of dislocations in icosahedral quasicrystals are comprehensively reviewed,

200 Examples of stable binary icosahedral quasicrystals are relatively rare, and at pr

201 In our previous studies, icosahedral quasicrystals have been synthesized and reco

202 use scattering, observed in all the 'stable' icosahedral quasicrystals studied so far.

203 we clarify the shock synthesis mechanism of icosahedral quasicrystals through two new shock recovery

204 Five-component icosahedral quasicrystals with compositions in the range

205 erials, numerous micron-sized five-component icosahedral quasicrystals, average composition Al72Cu12F

206 Using electron cryomicroscopy and icosahedral reconstruction of mutants that express pUL17

207 l and have dimensions similar to that of the icosahedral Ross River virus, the present results indica

208 ermost VP2 core shell of the triple-layered, icosahedral rotavirus particle surrounds the viral genom

209 058-nucleotide plus-strand RNA genome of the icosahedral satellite tobacco mosaic virus (STMV) using

210 The solid-state and gas-phase studies of the icosahedral Sb@M12@Sb20(n-/n+) ions show that the cluste

211 e space and supports the proposal that, like icosahedral Sc12Zn88, binary quasicrystalline phases may

212 Icosahedral seeds are used to dictate the growth of 3D e

213 gents play critical roles in stabilizing the icosahedral shape with {111} surfaces.

214 0-A spherical procapsid condenses to a 400-A icosahedral-shaped capsid with associated specific auto-

215 determined that EncA self-assembles into an icosahedral shell 32 nm in diameter (26 nm internal diam

216 We computationally study how an icosahedral shell assembles around hundreds of molecules

217 180 envelope glycoproteins that make up the icosahedral shell.

218 Bacteriophage capsids constitute icosahedral shells of exceptional stability that protect

219 ssed core protein assembles into T=3 and T=4 icosahedral shells, and atomic coordinates are available

220 However, the tail-less, icosahedral, single-stranded DNA PhiX174-like coliphages

221 EM to produce an electron density map of the icosahedral Sputnik virus at 3.5-A resolution, sufficien

222 EhV-202 has a 160- to 180-nm-diameter icosahedral structure and a genome of approximately 407

223 ns showed that the virus retains its overall icosahedral structure at this mildly acidic pH, except i

224 entional Au nanoparticles, as well as the bi-icosahedral structure of [Au38(SCH2CH2Ph)24].

225 The icosahedral structure, at 3.7-A resolution, resolves loo

226 escribed herein have 160- to 180-nm diameter icosahedral structures, have genomes of approximately 40

227 cages that self-assemble in vivo into stable icosahedral structures.

228 cupies positions beneath the vertices of the icosahedral surface shell, and the other is distributed

229 other known naturally occurring mineral with icosahedral symmetry (though the latter composition had

230 sicrystalline phase displaying face-centered icosahedral symmetry and low phason strain.

231 Both particles display T=3 icosahedral symmetry and nearly identical solid capsid s

232 ems such as spherical viruses, which utilize icosahedral symmetry as a guiding principle for the asse

233 what happens when an antibody binds near an icosahedral symmetry axis.

234 atellite Tobacco Necrosis Virus, except that icosahedral symmetry constraints could be removed to rev

235 HAstV particles display T=3 icosahedral symmetry formed by 180 copies of the capsid

236 However, whether icosahedral symmetry is maintained along the transition

237 Similar deviations from icosahedral symmetry may be biologically significant dur

238 the subunit into a procapsid with T=7 laevo icosahedral symmetry named Prohead-I.

239 particle clusters with local tetrahedral or icosahedral symmetry that seed growth of the temporally

240 Orsay capsid has a T = 3 icosahedral symmetry with 60 trimeric surface spikes.

241 ions of the capsid are possible based on its icosahedral symmetry, but the surrounding tegument and e

242 building blocks, which are able to pack with icosahedral symmetry, we examine how stable these highly

243 atomic model of the alphavirus envelope with icosahedral symmetry.

244 significant fraction of VP1 can deviate from icosahedral symmetry.

245 llowing fJAM-A binding, leading to a loss of icosahedral symmetry.

246 k tightly to form a smooth protein coat with icosahedral symmetry.

247 riophage P22, reconstructed without imposing icosahedral symmetry.

248 ike particles, which is characteristic of an icosahedral T = 1 symmetry.

249 intermediates comprising some 11 dimers, and icosahedral T = 3 capsids made up of 90 dimers.

250 nically induce partial disassembly of single icosahedral T=1 capsids and virions of the minute virus

251 Pores that are 7 A in diameter form around icosahedral threefold symmetry axes.

252 y conserved in all AAVs: depressions at each icosahedral two-fold symmetry axis and surrounding each

253 ough one of the large pores that open at the icosahedral twofold axes, and is transferred along a con

254 her of face-centred-icosahedral or primitive-icosahedral type, and the positions of their atoms have

255 Turret-like densities were found on icosahedral vertices and may represent a unique adaptati

256 bly intermediates, which become the capsid's icosahedral vertices.

257 tions that are ultimately occupied by 5-fold icosahedral vertices.

258 undetected protein was found to underlie the icosahedral vertices: this is tentatively assigned as a

259 erica serovar Typhimurium and is a model for icosahedral viral capsid assembly.

260 Icosahedral viral capsids are made of a large number of

261 Icosahedral viral capsids are obligated to perform a the

262 assemblies required for the formation of the icosahedral viral envelope.

263 rotein of norovirus VP1 assembles to form an icosahedral viral particle.

264 eractions outside the dimer interface in the icosahedral virion.

265 Iflaviruses have nonenveloped icosahedral virions containing single-stranded RNA genom

266 The Megaviridae exhibit pseudo-icosahedral virions up to 0.7 mum in diameter and adenin

267 s, tentatively named Metallosphaera turreted icosahedral virus (MTIV), that was isolated from an acid

268 l host cells infected by Sulfolobus turreted icosahedral virus (STIV) and Sulfolobus islandicus rod-s

269 Host cells infected by Sulfolobus turreted icosahedral virus (STIV) have been shown to produce unus

270 and the infecting virus Sulfolobus turreted icosahedral virus (STIV) is one of the well-established

271 Sulfolobus turreted icosahedral virus (STIV) was isolated in acidic hot spri

272 Sulfolobus turreted icosahedral virus (STIV), an archaeal virus that infects

273 infect archaea, such as Sulfolobus turreted icosahedral virus and halophage SH1.

274 Icosahedral virus assembly requires a series of concerte

275 ons at subnanometer (<10-A) resolution of an icosahedral virus assembly were obtained by cryogenic el

276 ly of hundreds of identical proteins into an icosahedral virus capsid is a remarkable feat of molecul

277 ents for essential biochemical reactions and icosahedral virus capsids, which encapsidate and protect

278 lishment of a productive Sulfolobus turreted icosahedral virus infection.

279 that the archaeal virus Sulfolobus turreted icosahedral virus isolated from Yellowstone National Par

280 Icosahedral virus particles constitute paradigms to stud

281 een shown to assemble trimer-clustered T = 3 icosahedral virus particles.

282 ne circovirus 2 (PCV2) is a T=1 nonenveloped icosahedral virus that has had severe impact on the swin

283 elia capensis omega virus (NomegaV) is a T=4 icosahedral virus that undergoes a dramatic maturation i

284 llite tobacco mosaic virus (STMV) is a T = 1 icosahedral virus with a single-stranded RNA genome.

285 rt the multivalent display of the A-helix on icosahedral virus-like particles (VLPs) derived from the

286 te and polynorbornene (PNB) when attached to icosahedral virus-like particles.

287 e to infection with the S ulfolobus turreted icosahedral virus.

288 tions have implications for the evolution of icosahedral viruses and regulation of virus assembly.

289 STMV is among the simplest of the icosahedral viruses but, nonetheless, has an RNA genome

290 he last twenty years, numerous giant, dsDNA, icosahedral viruses have been discovered and assigned to

291 How icosahedral viruses regulate the release of viral RNA in

292 nt head assembly gives guidance to how other icosahedral viruses reproducibly assemble into capsids w

293 ANCE The Parvovirinae are small nonenveloped icosahedral viruses that are important pathogens in many

294 The Parvovirinae are small nonenveloped icosahedral viruses that are important pathogens in many

295 Many icosahedral viruses undergo large-scale conformational t

296 Many icosahedral viruses use a specialized portal vertex to c

297 However, a mechanistic understanding of how icosahedral viruses utilize this process to transform im

298 For the icosahedral viruses, good agreement was also found betwe

299 " fold similar to that found in many diverse icosahedral viruses, including archaeal, bacterial, plan

300 Unlike the capsids of icosahedral viruses, retroviral capsids are pleomorphic,