ライフサイエンスコーパス: coat protein

1 an be composed of either 90 or 120 dimers of coat protein.

2 ter enzymes covalently attached to the pVIII coat protein.

3 movement of RNA-CP, which encodes the virus coat protein.

4 Here, we identify partners in coat protein.

5 mediate conformational switches in the viral coat protein.

6 second-site suppressors located in the viral coat protein.

7 of the scaffolding protein to interact with coat protein.

8 tants in YidC and in the model substrate Pf3 coat protein.

9 or fission, processes that are regulated by coat proteins.

10 ay presents polypeptides as fusions to phage coat proteins.

11 lipid and cholesterol monolayer and specific coat proteins.

12 eplicated genomes be completely protected by coat proteins.

13 assembly using GFP-fusions to 41 B. subtilis coat proteins.

14 t gathered from in vitro studies of purified coat proteins.

15 ution conformations upon addition of cognate coat proteins.

16 of atALKBH9B to interact (or not) with their coat proteins.

17 lical arrangements of thousands of identical coat proteins.

18 of perilipin 5 (PLIN5), a lipid droplet (LD) coating protein.

19 t allows them to bind specific antibodies on coat protein 3 (p3) and multiple biotin groups on coat p

20 protein 3 (p3) and multiple biotin groups on coat protein 8 (p8) to bind to avidin-conjugated enzymes

21 er peptide expression on the p3 or on the p8 coat proteins, a corresponding density of 5 up to more t

22 y expressed, we observed a reduction in BaMV coat protein accumulation to 47% and 27% that of the wil

23 rticles (146 S; 8200 kDa) or pentameric FMDV coat protein aggregates (12 S; 282 kDa) was detected, a

24 nd postfusion states of the HIV-1 gp41 viral coat protein, although very different from one another,

25 hering system based on the MS2 bacteriophage coat protein and a reporter construct containing an MS2-

26 mes (ORF1 and ORF2), which encode a putative coat protein and an RNA-dependent RNA polymerase (RdRp),

27 The coat protein and NIa-Pro encoded by these two viruses, w

28 nome packaging triggers rearrangement of the coat protein and release of scaffolding protein, resulti

29 and by polar virions that contain the minor coat protein and TGB1 attached to one extremity.

30 Furthermore, we characterized the PP7 coat protein and the binding to its respective RNA stem

31 virus particles in solutions containing the coat protein and the single-stranded RNA of the virus.

32 el incorporates membrane-bound compartments, coat proteins and adaptors that drive vesicles to bud an

33 NA, termed "packaging signals" (PS), contact coat proteins and facilitate efficient capsid assembly.

34 formation by interacting with its cargo and coat proteins and has significant implications in VLDL s

35 uding several extracellular proteins, as egg coat proteins and inner ear tectorins.

36 operative supramolecular process between the coat proteins and the nucleic acids, which is based on r

37 They control the recruitment of coat proteins, and modulate the structure of actin filam

38 in the absence of coat protein, whereas the coat protein appears to control fidelity.

39 We showed how different coat proteins are distributed within the coat structure

40 Their binding sites on the coat proteins are evolutionarily conserved across the Pa

41 zed for Bacillus sp., but Bacillus sp. spore coat proteins are poorly conserved in Clostridium sp.

42 These internalized coat proteins are the most asymmetrically arranged major

43 as encasement, involves the migration of the coat proteins around the circumference of the spore in s

44 Using the membrane-bound form of the fd coat protein as a model membrane protein and its experim

45 'full virus vector strategy' with the viral coat protein as fusion partner for the designed antimicr

46 of D302A are perpetuated in the full-length coat protein as shown by a higher sensitivity to proteas

47 F-pilus, has a T = 3 icosahedral lattice of coat proteins assembled around its 4,217 nucleotides of

48 proteins that are functional analogs of the coat protein assemblies that mediate intracellular vesic

49 e of alpha-helices and replaces one dimer of coat proteins at a twofold axis.

50 na pollen-borne CRPs, the PCP-Bs (for pollen coat protein B-class) that are related to embryo surroun

51 l design for a self-assembling minimal viral coat protein based on simple polypeptide domains.

52 otein disulfide isomerase (PDI) and the COPI coat protein beta-COP.

53 ith the modified BaMV RNA containing the MS2 coat protein binding sequence.

54 3 and Lys-296 are particularly important for coat protein binding.

55 The coat protein-binding domain of scaffolding protein is a

56 The results show that p37, the viral coat protein, blocks RNA silencing.

57 oteomics studies reveal that VLPs lack viral coat proteins but possess a pharmacopoeia of (1) the euk

58 ant virions, peptides were released from the coat protein by chemical cleavage.

59 ne proteins termed caveolins and cytoplasmic coat proteins called cavins.

60 ntigen binding, the approximately 4000 other coat proteins can be augmented-by either chemical functi

61 icle biogenesis machinery components such as coat proteins can interact with the actin cytoskeleton f

62 ese viruses, when modified by changing their coat protein, can infect axolotl cells only when they ha

63 s of the plasma membrane-associated caveolar coat proteins caveolin3 and cavin1 were both not reduced

64 or expression of specific peptides on phage coat proteins, characterization of engineered phages in

65 atalytic activity and binding to the vesicle coat protein clathrin are essential for OCRL1 function i

66 ets an endocytic mechanism that involves the coat protein clathrin, because SA interfered with the cl

67 are both largely free of the classical Golgi coat proteins coatomer (COPI) and clathrin.

68 xes originated from vesicle coats similar to coat protein complex (COP) I, COPII, and clathrin.

69 further demonstrate that TRAPPIII binds the coat protein complex (COP) II coat subunit Sec23.

70 ction while reducing CFTR's interaction with coat protein complex 1 (COP1).

71 The ADP ribosylation factor (Arf) and the coat protein complex I (COPI) are involved in vesicle tr

72 Unexpectedly, coat protein complex I (COPI) is required for lipid drop

73 n ERManI and gamma-COP, the gamma subunit of coat protein complex I (COPI) that is responsible for Go

74 ads to defective intracellular transport via coat protein complex I (COPI), we show that COPA variant

75 We found that knockdown of the coat protein complex I (COPI)-Arf79F (also known as Arf1

76 We have shown that coat protein complex I (COPI)-dependent trafficking, an

77 We investigated the relevance to AD of coat protein complex I (COPI)-dependent trafficking, an

78 resident proteins for retrieval to the ER in coat protein complex I-formed transport carriers.

79 Furthermore, knockdown of coat protein complex II (COPII) component SEC24D, which

80 coincides with an up-regulation of the inner coat protein complex II (COPII) components SEC23B, SEC24

81 les from the endoplasmic reticulum (ER), the coat protein complex II (COPII) is also responsible for

82 The coat protein complex II (COPII) is essential for the tra

83 Coat protein complex II (COPII) mediates formation of th

84 The conserved coat protein complex II (COPII) mediates the initial ste

85 ransport vesicles generated by the essential coat protein complex II (COPII) proteins.

86 ticulum (ER), but we find, using a cell-free coat protein complex II (COPII) vesicle budding reaction

87 hat CUPS lack Golgi enzymes, but contain the coat protein complex II (COPII) vesicle tethering protei

88 During the budding of coat protein complex II (COPII) vesicles from transition

89 23 homolog B (S. cerevisiae), a component of coat protein complex II (COPII), which transports protei

90 ramolecular cargo procollagen is loaded into coat protein complex II (COPII)-coated carriers at endop

91 endoplasmic reticulum (ER) is facilitated by coat protein complex II (COPII).

92 gene, which encodes a core component of the coat protein complex II (COPII).

93 nd vesicles that are formed by the cytosolic coat protein complex II (COPII).

94 specific for each enzyme, and independent of coat protein complex II and I (COPII and COPI).

95 SERT relies exclusively on the coat protein complex II component SEC24C for endoplasmic

96 hesis with upregulation of secretory pathway coat protein complex II components.

97 of HSP90 is required prior to recruitment of coat protein complex II components.

98 s are consistent with the proposed chaperone/coat protein complex II exchange model.

99 o be recognized by distinct sites within the coat protein complex II machinery.

100 of the endoplasmic reticulum/Golgi transport coat protein complex II Sec proteins.

101 ulates the association between CREBH and the coat protein complex II transport vesicle and thus contr

102 isingly, the mutated gene, SEC24A, encodes a coat protein complex II vesicle coat subunit involved in

103 ynthesized secretory proteins require COPII (coat protein complex II) to exit the endoplasmic reticul

104 e protein Atg9 (autophagy-related 9), COPII (coat protein complex II) vesicles, and possibly other so

105 The SEC23 protein is a core component of coat protein complex II-coated vesicles, which transport

106 ein is inhibited indicating its transport in coat protein complex II-coated vesicles.

107 iana tabacum) initially involves a canonical coat protein complex II-dependent endoplasmic reticulum-

108 erone calnexin, altered association with the coat-protein complex II component Sec24D, and thereby im

109 tes protein translation into the ER, and the coat protein complexes (COPI and COPII), which mediate v

110 ansport, where they nucleate the assembly of coat protein complexes at sites of carrier vesicle forma

111 Cytoplasmic coat protein complexes perform central roles in sorting

112 Cargo adaptor subunits of vesicle coat protein complexes sort transmembrane proteins to di

113 rafficking between organelles is achieved by coat protein complexes, coat protomers, that bud vesicle

114 inations is mediated by a number of distinct coat protein complexes, including adaptor protein 1 (AP-

115 articular, we show that the increasing viral coat protein concentration that occurs in infected cells

116 ch the scaffolding protein induces a single, coat protein conformational switch and not a series of s

117 nternal scaffolding protein and three in the coat protein constitute the core of the B protein bindin

118 the analyses demonstrated that the asbestos coating proteins contain high levels of beta-sheet struc

119 I-domain was investigated by generating the coat protein core without its I-domain and the isolated

120 re route due to the acquisition of a surface coating (protein corona) that is determined by the route

121 in B. subtilis led us to identify two spore coat proteins, CotB and CotG, as CotH substrates.

122 B. subtilis coat proteins (CotY, CotE, CotV and CotW) expressed in E

123 by using BSMV silencing vectors defective in coat protein coupled with introducing fungal gene sequen

124 sing Pfs25 fused to the Alfalfa mosaic virus coat protein (CP) and produced these non-enveloped hybri

125 oding for the replication protein (Rep), the coat protein (cp) and the movement protein (mp), as well

126 ons is unknown, since 180 copies of the same coat protein (CP) encapsidate each of the BMV genomic RN

127 receptor for pea enation mosaic virus (PEMV) coat protein (CP) in the gut of the pea aphid, Acyrthosi

128 We have examined the roles of RNA-coat protein (CP) interactions in the assembly of satell

129 In this study, we demonstrated that the coat protein (CP) of Wheat streak mosaic virus (WSMV; ge

130 y upstream of the Turnip crinkle virus (TCV) coat protein (CP) open reading frame (ORF) has been foun

131 everal hundred copies of a helically arrayed coat protein (CP) protecting a (+)ssRNA.

132 etion of the first eight residues of the BMV coat protein (CP) resulted in the RNA1-containing partic

133 structure of the C-terminal truncated PapMV coat protein (CP) reveals a novel all-helix fold with se

134 fected with TriMV expressing WSMV NIa-Pro or coat protein (CP) substantially excluded superinfection

135 Its genome encodes only its coat protein (CP) subunit, relying on the polymerase of

136 Coat protein (CP)- transgenic papaya lines resistant to

137 The results suggest that the same coat protein (CP)-RNA and maturation protein (MP)-RNA in

138 on the 5 end confers affinity for the Qbeta coat protein (CP).

139 fected cells contained very small amounts of coat protein despite an abundance of RNA2.

140 ss the model proteins and bacteriophage MS2 (coat protein), differing widely in structure, methionine

141 This coat protein dimer binds to the gRNA and interacts with

142 Unexpectedly, we found a coat protein dimer sequestered in the interior of the vi

143 d with one maturation protein monomer and 89 coat protein dimers arranged in a T = 3 icosahedral latt

144 rms a genome-delivery apparatus and joins 89 coat protein dimers to form a capsid.

145 Using novel genetically-fused coat protein dimers, we have been able to trap higher-or

146 s with a stronger response against the PopMV coat protein due to enhanced activation sensitivity.

147 type vaccines engineered to direct the HIV-1 coat protein Env to dendritic cells.

148 hanisms coupling pH transitions to endosomal coat protein exchange; discovery of distinct pH threshol

149 al capsids are a prototypical example, where coat proteins exhibit not only self-interactions but als

150 Our coat protein features precise control over the cooperati

151 ssembly mutations, which act on the level of coat protein flexibility.

152 sinaiiensis tailed virus 1 has the canonical coat protein fold of HK97.

153 opy, and image reconstruction that the major coat protein fold of newly isolated archaeal Haloarcula

154 of these common features include a conserved coat protein fold, an internal lipid membrane, and a DNA

155 t as an intramolecular chaperone because the coat protein folds independently, and many folding mutan

156 into a lattice, suggesting that it acts as a coat protein for AP-3 in formation of the regulated secr

157 otein such as a plant lectin or a luteovirus coat protein for transcytosis across the gut epithelium,

158 ette of synonymous MS2 RNA motifs and tandem coat proteins for RNA imaging and showed a dramatic impr

159 y to immobilize sodium dodecyl sulfate (SDS)-coated proteins for fully integrated microfluidic Wester

160 Viral coat proteins function in virion assembly and virus biol

161 tected by co-expression of bacteriophage MS2 coat protein fused with EGFP.

162 In this study we use a library of 41 spore coat proteins fused to the green fluorescent protein to

163 rs then recruit the corresponding MS2 or PP7 coat proteins fused with different fluorescent proteins

164 His-154 of the coat protein Gag forms an m(7)Gp adduct, and the H154R m

165 In cultured neurons, we found that the HIV coat protein gp120 increased the transcriptional express

166 ntify the molecular events evoked by the HIV coat protein gp120 that facilitate the intraneuronal acc

167 In bacteriophage P22, only coat protein (gp5) and scaffolding protein (gp8) are nee

168 ved low levels of identity between the spore coat protein H (CotH), and the Fam20C-related secretory

169 The bacteriophage P22 coat protein has the common HK97-like fold but with a ge

170 vesicles derived from subcomplexes of COPII coat proteins have a role in the specialized trafficking

171 teins), also known as SCP superfamily (sperm-coating proteins), have been implicated in many physiolo

172 These procapsids are assembled from a coat protein having the HK97 fold in a reaction driven b

173 ancement, as well as directly coding for the coat protein, highlighting the density of encoded functi

174 otein 27 (FSP27, CIDEC in humans) is a lipid-coating protein highly expressed in mature white adipocy

175 Here we determined that spore coat protein homologs (CotH) of Mucorales act as fungal

176 Here we show that the coat protein I (COPI) complex sorts anterograde cargoes

177 hich identified at least two subunits of the coat protein I (COPI) complex.

178 In contrast, cytosolic coat protein I (COPI) vesicle coat mutations in sey1Delt

179 ane recruitment of coatomer and formation of coat protein I (COPI)-coated vesicles is crucial to home

180 iated by clathrin-coated vesicles, while the COat Protein I and II (COPI and COPII) routes stand for

181 ic reticulum to the Golgi is mediated by the coat protein II (COPII) complex comprising a Sec23-Sec24

182 Coat protein II (COPII)-coated vesicles transport protei

183 The coat protein II (COPII)-coated vesicular system transpor

184 ere glycoprotein cargo concentrates prior to coat protein II vesicle-mediated transport to the Golgi.

185 /cTAGE5 receptor can bind multiple copies of coat protein in a close-packed array.

186 Perilipin 1, the most abundant lipid-coat protein in adipocytes, plays a key role in regulati

187 structure of the membrane-bound form of Pf1 coat protein in explicit lipid bilayers using the recent

188 ional changes of uniformly (15)N-labeled Pf1 coat protein in native-like bilayers.

189 ES activity and produces low levels of viral coat protein in vitro and in vivo Our findings may be ap

190 ics that these RNA segments are bound to the coat proteins in a sequence-specific manner.

191 make important intersubunit contacts between coat proteins in adjacent capsomers.

192 posed, which facilitates assembly by binding coat proteins in such a way that they promote the protei

193 highlights the important function of surface coat proteins in the interplay between complement regula

194 ) is one of the most abundantly expressed LD-coating proteins in skeletal muscle.

195 Vesicle coat proteins, including coatomer-I subunits, localize t

196 oating of the sensor polymers by recombinant coat proteins induces their stretching due to steric hin

197 Luteovirid coat protein-insect neurotoxin fusions represent a promi

198 and identified three conserved motifs of RNA-coat protein interactions among 15 of these stem-loops w

199 In this system, coat protein interacts with an internal scaffolding prot

200 elevating the protein levels with which the coat protein interacts, were used to elucidate pleiotrop

201 TGB1 mediated insertion of the viral coat protein into PD, probably by its interaction with t

202 y as a guiding principle for the assembly of coat proteins into a capsid shell.

203 proteins with similar features to eukaryotic coat proteins involved in vesicle biogenesis.

204 One LD coat protein is caveolin-1 (Cav-1), an essential compone

205 rosine residues precisely fused to the major coat protein is converted into a photo-responsive organi

206 e that the binding of scaffolding protein to coat protein is dependent on angle of the beta-turn and

207 The luteovirid coat protein is sufficient for delivery of fused protein

208 midgut homeostasis by the mammalian parasite coat proteins is a novel function and indicates that VSG

209 hage P22, the association of scaffolding and coat proteins is mediated mainly by ionic interactions.

210 ces parallel to the membrane that buckle the coat protein layer, generated by an actomyosin contracti

211 he center; 2), the inherent curvature of the coat-protein layer; and 3), forces parallel to the membr

212 and Ubp7 resulted in elongation of endocytic coat protein lifetimes at the plasma membrane and recrui

213 ained and tunable release, while the surface-coated protein ligands (e.g., transferrin) were demonstr

214 ecruit fusion proteins consisting of the MS2 coat protein linked to transcription activation domains,

215 that the respective roles of scaffolding and coat proteins may have been redistributed during the evo

216 Lipid droplet (LD)-coating proteins may control proper lipid storage in ske

217 to coexpress a fluorescent MS2 bacteriophage coat protein (MCP) and an RNA of interest tagged with mu

218 rt-lived mRNAs, the tight binding of the MS2 coat protein (MCP) to the MS2 binding sites (MBS) protec

219 This mode of dual signal binding to a single coat protein might serve as a general mechanism to trigg

220 ons that abolish the salt bridge destabilize coat protein monomers and impair capsid self-assembly, b

221 was achieved by the stepwise acquisition of coat protein mutations.

222 esis of genes 5 and 8, we show that changing coat protein N-arm residue 14 from aspartic acid to alan

223 To a lesser extent, coat protein N-arm residue E18 is also implicated in the

224 periplasm requires binding between the minor coat protein named pIII and a bacterial inner-membrane r

225 However, the levels of the coat protein needed for consistent labeling of mRNAs lim

226 A lattice of coat protein nucleates at each of the 5-fold vertices, b

227 Here we use the coat protein of a luteovirus, an aphid-vectored plant vi

228 noparticles (PapMV), self-assembled from the coat protein of a plant virus and a noncoding ssRNA mole

229 that the I domain that is inserted into the coat protein of bacteriophage P22 is important in the pr

230 CAV1, the principal coat protein of caveolae, has been associated with the r

231 blocking its binding to Caveolin-1, the main coat protein of caveolae, using a highly specific peptid

232 VP1 is the major coat protein of murine polyomavirus and forms virus-like

233 virtually complete de novo assignment of the coat protein of Pf1 virus.

234 The coat protein of positive-stranded RNA viruses often cont

235 gnate pathogen-derived effector protein, the coat protein of potato virus X.

236 r protein (AP) complexes are the predominant coat proteins of membrane vesicles in post-Golgi traffic

237 sponse, by genetically engineering the major coat proteins of the phage.

238 ted several second-site mutations in the p38 coat protein open reading frame (ORF) that arose in resp

239 m, through fusion of various epitopes to the coat protein or as adjuvant to enhance humoral immune re

240 The polymerase (ORF1) and coat protein (ORF4) genes shared 31 to 49% nucleotide an

241 FLAG-tag antibody binding peptides on their coat protein outer surfaces, making them selective biose

242 ent genetically encoded ligands on the major coat protein, P8.

243 During morphogenesis, varphiX174 coat protein participates in at least four well-defined

244 t of members of the Brassicaceae, the pollen coat proteins (PCPs), are emerging as important signalli

245 The detected PRSV coat protein PCR product was sequenced and the nucleotid

246 ng elements including a newly developed PRSV coat protein PCR.

247 otein interactions between CGI-58 and the LD coating protein perilipin 1 restrain the ability of CGI-

248 the N-terminal domain of the CTXvarphi minor coat protein pIII (pIII-N1) and the C-terminal domain of

249 mors, we found an increased expression of LD coat protein PLIN2 compared with normal colonic epitheli

250 Perilipin 1 is a lipid droplet coat protein predominantly expressed in adipocytes, wher

251 -scaffolding-protein virus assembly systems, coat proteins promiscuously interact to form heterogeneo

252 Disruption of either the RNA coat protein recognition motif or its contact amino acid

253 We show that the sequences of coat protein recognition motifs within multiple, dispers

254 Coat protein residue D14 is shown by cross-linking to in

255 distinctive helical array of the COPII inner coat protein Sec23/24*Sar1; the helical arrangement is a

256 ecognition of cytosolic signals by the COPII coat protein, Sec24.

257 ermore, we show that PPP motifs in the outer coat protein Sec31 also bind to Sec23, suggesting that s

258 the external scaffolding protein acts like a coat protein, self-associating into large aberrant spher

259 which asymmetrically expands the surrounding coat protein shell to potentially facilitate RNA release

260 The core coat protein shows a pronounced folding defect.

261 D111 and E113, form salt bridges with basic, coat protein side chains.

262 protein with acidic residues in the N-arm of coat protein, since this interaction has been shown to b

263 s thermodynamic stability to the full-length coat protein so that it can fold reasonably efficiently

264 a comparison of particle morphologies, major coat protein structures, and gene content among the five

265 A) wrapped by thousands of copies of a major coat protein subunit (the capsid).

266 es reveal the C-terminal region of the small coat protein subunit, which is essential for virus assem

267 The coat protein subunits are mostly alpha-helical and curve

268 g polymerized actin and curvature-generating coat proteins such as clathrin.

269 in this process, although other adaptors and coat proteins, such as AP-4, ARH, Numb, exomer, and retr

270 ding capacity of B2 somehow played a role in coat protein synthesis.

271 main is a genetic insertion in the phage P22 coat protein that chaperones its folding and stability.

272 an insertion domain of the bacteriophage P22 coat protein that drives rapid folding and accounts for

273 utively associated cytoplasmic lipid droplet coat protein that has been implicated in fatty liver for

274 n the test fragment, encodes a region of the coat protein that undergoes a conformational change upon

275 ily of plant-specific, LD surface-associated coat proteins that are required for proper biogenesis of

276 Many viruses encode scaffolding and coat proteins that co-assemble to form procapsids, which

277 mbrane determinants for assembly of clathrin coat proteins that drive formation of clathrin-coated ve

278 ved a structural rearrangement in the capsid coat proteins that is required to package the viral gRNA

279 Owing to extensive cross-linking among coat proteins, this structure has been recalcitrant to d

280 These switches direct the coat protein through early assembly.

281 manipulated to express the receptor for that coat protein, thus allowing for the possibility of targe

282 d sigma(K) control the adherence of the CotB coat protein to C. difficile spores, indicating that the

283 ent addition and conformational switching of coat proteins to the growing capsid we believe is cataly

284 ANGO1/cTAGE5 promotes the accretion of inner coat proteins to the helical lattice.

285 nes and Myzus persicae-feed on a recombinant coat protein-toxin fusion, either in an experimental mem

286 type lectin-like domain (CTLD) and the sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) domain, al

287 reveal the crystal structures of mollusk egg coat protein, VERL, complexed with cognate sperm protein

288 ell binding observed for the wild-type virus coat protein VP1.

289 of the BC and HI loops as found in the viral coat protein, VP1, of BKV.

290 this family are those that lack the internal coat protein, VP4.

291 t and pantropic infectivity, mediated by its coat protein, VSV-G.

292 rison, a molecular dynamics simulation of fd coat protein was also performed without any restraints.

293 in the association of scaffolding protein to coat protein was dependent on location, with substitutio

294 Studying the MS2 coat protein, we decompose the binding energy contributi

295 hat clathrin heavy chain (CHC-1), a membrane coat protein well known for its role in receptor-mediate

296 rrant spherical structures in the absence of coat protein, whereas the coat protein appears to contro

297 mino-acid accessory domain inserted into its coat protein, which has the canonical HK97 protein fold.

298 1 hydrogenase prior to expression of the P22 coat protein, which subsequently self assembles.

299 ed the interaction of NLS-GFP-MS2 (phage MS2 coat protein) with the modified BaMV RNA containing the

300 r of RNA directly contacts every copy of the coat protein, with one-third of the interactions occurri