ライフサイエンスコーパス: cryoelectron microscopy

1 pase-8 tDED filament structure determined by cryoelectron microscopy.

2 homo-tetrameric structure has been solved by cryoelectron microscopy.

3 ight of structural data recently obtained by cryoelectron microscopy.

4 ay mass spectrometry, and negative stain and cryoelectron microscopy.

5 pected "fan blade" motifs when visualized by cryoelectron microscopy.

6 zed the structure of the furin precursor, by cryoelectron microscopy.

7 in the GR:Hsp70:Hsp90:Hop complex imaged by cryoelectron microscopy.

8 uited to two-dimensional class averages from cryoelectron microscopy.

9 (3.3 angstrom) states using single-particle cryoelectron microscopy.

10 and peripentonal triplexes as visualized by cryoelectron microscopy.

11 complexed with Fab fragments of CR4354 using cryoelectron microscopy.

12 cking gp17, gp50, or gp65 were determined by cryoelectron microscopy.

13 largely due to technological innovations in cryoelectron microscopy.

14 l structures of both GCRV core and virion by cryoelectron microscopy.

15 n in a "D6 barrel" cage assembly measured by cryoelectron microscopy.

16 of a filamentous virus, bacteriophage fd, by cryoelectron microscopy.

17 hedral plant virus, was resolved to 8.5 A by cryoelectron microscopy.

18 esence of four gold clusters was verified by cryoelectron microscopy.

19 tre-LH1-PufX complexes have been analysed by cryoelectron microscopy.

20 e FKBP12.6-binding site mapped previously by cryoelectron microscopy.

21 imilar to the ribosome-bound RF2 observed by cryoelectron microscopy.

22 ed by either x-ray crystallographic study or cryoelectron microscopy.

23 receptor (PVR or CD155), were determined by cryoelectron microscopy.

24 sid protein and nucleic acid were studied by cryoelectron microscopy.

25 multicomponent death machine, deciphered by cryoelectron microscopy.

26 mmine cobalt (III) have been investigated by cryoelectron microscopy.

27 using site-specific mutagenesis, followed by cryoelectron microscopy.

28 (KSHV) was visualized at 24-A resolution by cryoelectron microscopy.

29 heir identity as procapsids was confirmed by cryoelectron microscopy.

30 s and imaged in the frozen-hydrated state by cryoelectron microscopy.

31 density, and particle morphology by scanning cryoelectron microscopy.

32 n studied by means of three-dimensional (3D) cryoelectron microscopy.

33 D structure of bR from x-ray diffraction and cryoelectron microscopy.

34 thermophilus ribosome has been determined by cryoelectron microscopy.

35 in high-resolution structural information by cryoelectron microscopy.

36 rane without disrupting it, as visualized by cryoelectron microscopy.

37 ned the structure of the C5-CirpT complex by cryoelectron microscopy.

38 virions before and after DNA ejection using cryoelectron microscopy.

39 tive state in HeLa cells enabled by cellular cryoelectron microscopy.

40 from Nav1.7 using X-ray crystallography and cryoelectron microscopy.

41 interface, both resolved by high-resolution cryoelectron microscopy.

42 protein-ligand complex to 3.6 angstrom with cryoelectron microscopy.

43 ts, Ac1-140, Ac1-122, and Ac1-103, solved by cryoelectron microscopy.

44 A cryoelectron microscopy 8.5 A resolution map of the 1,90

45 Here we use biochemical and cryoelectron microscopy analyses to show that the amino-

46 and murine TRPC6, were recently resolved by cryoelectron microscopy analysis, structural changes dur

47 supports the results of a previous report of cryoelectron microscopy analysis.

48 By direct electron-counting cryoelectron microscopy and asymmetric reconstruction, w

49 Cryoelectron microscopy and biochemical analyses show th

50 Using cryoelectron microscopy and biochemistry, we show that R

51 In this study, cryoelectron microscopy and computer modeling provide ev

52 By using cryoelectron microscopy and correlation averaging, diffe

53 as been determined by using a combination of cryoelectron microscopy and fitting of the known structu

54 his problem, we coupled direct techniques of cryoelectron microscopy and fluorescence microscopy with

55 We also used cryoelectron microscopy and helical image analysis to de

56 Here, we use cryoelectron microscopy and helical image analysis to vi

57 ion of the stacked disk obtained by means of cryoelectron microscopy and helical image processing.

58 By using cryoelectron microscopy and helical image reconstruction

59 otide-dependent conformational changes using cryoelectron microscopy and image analysis.

60 ional structure of isoform 3 was obtained by cryoelectron microscopy and image enhancement techniques

61 ructure of the mutant RNAP was determined by cryoelectron microscopy and image processing of frozen-h

62 Cryoelectron microscopy and image reconstruction analysi

63 Transmission cryoelectron microscopy and image reconstruction of r-co

64 to 16 and 25 A resolution, respectively, by cryoelectron microscopy and image reconstruction techniq

65 In this study, we used cryoelectron microscopy and image reconstruction to show

66 We have used cryoelectron microscopy and image reconstruction to stud

67 ) and visualized at 24-A resolution by using cryoelectron microscopy and image reconstruction.

68 ave visualized its precursor, Prohead-II, by cryoelectron microscopy and modeled the conformational c

69 In this issue of Cell, Ma et al. use cryoelectron microscopy and modeling to define doublet m

70 ganded) and CD4-induced (liganded) states by cryoelectron microscopy and molecular modeling.

71 Using cryoelectron microscopy and other biophysical and bioche

72 Cryoelectron microscopy and reconstruction localized the

73 nce microscopy, atomic force microscopy, and cryoelectron microscopy and review recent studies that u

74 Using ATP-stabilised p53, we have employed cryoelectron microscopy and single particle analysis to

75 ee-dimensional (3D) structure, determined by cryoelectron microscopy and single particle analysis to

76 nt with a dimeric subunit stoichiometry, and cryoelectron microscopy and single particle analysis wit

77 Cryoelectron microscopy and single-particle analysis rev

78 se complex at 12 A resolution as obtained by cryoelectron microscopy and single-particle image recons

79 Cryoelectron microscopy and single-particle image recons

80 We have used cryoelectron microscopy and three-dimensional (3D) recon

81 ufficient for structural characterization by cryoelectron microscopy and three-dimensional (3D) recon

82 We used cryoelectron microscopy and three-dimensional image anal

83 We have used cryoelectron microscopy and three-dimensional image reco

84 Cryoelectron microscopy and tomography analyses revealed

85 Cryoelectron microscopy and tomography have been applied

86 fixation, thus exemplifying the potential of cryoelectron microscopy and tomography to reveal structu

87 Cryoelectron microscopy and X-ray crystallography have r

88 Structural resolution of Pv-M17 by cryoelectron microscopy and X-ray crystallography togeth

89 vitro, which include x-ray crystallography, cryoelectron microscopy, and NMR analyses by numerous gr

90 RyR2 by green fluorescent protein insertion, cryoelectron microscopy, and single-particle image proce

91 mental approaches such as fiber diffraction, cryoelectron microscopy, and three-dimensional reconstru

92 s 5 (PIV5) at 4.3- angstrom resolution using cryoelectron microscopy, as well as the oligomerization

93 We have used cryoelectron microscopy at approximately 11-A resolution

94 the Qbeta-MurA complex using single-particle cryoelectron microscopy, at 4.7-A, 3.3-A, and 6.1-A reso

95 A 7-A cryoelectron microscopy-based reconstruction of Sindbis

96 integrated structure-function approach using cryoelectron microscopy, biochemical kinetics, and force

97 t, as observed previously by single-particle cryoelectron microscopy, blocks 80S formation at a later

98 Cryoelectron microscopy can image pleomorphic structures

99 Crystallography and cryoelectron microscopy can reveal the structural relati

100 Cryoelectron microscopy (cryo-EM) analyses have shown th

101 NSP5 and RNA, we carried out single-particle cryoelectron microscopy (cryo-EM) analysis of NSP2 alone

102 tures derived from X-ray crystallography and cryoelectron microscopy (cryo-EM) for the 1095 strain of

103 gh-resolution structures into low-resolution cryoelectron microscopy (cryo-EM) maps is presented.

104 Here, we present cryoelectron microscopy (cryo-EM) maps of 80SCrPV-STOP e

105 tures and experimental electron density from cryoelectron microscopy (cryo-EM) measurements is then c

106 Recent cryoelectron microscopy (cryo-EM) of nodavirus RNA repli

107 Here a subnanometer asymmetric cryoelectron microscopy (cryo-EM) reconstruction of a co

108 In this study, we present a cryoelectron microscopy (cryo-EM) reconstruction of the

109 In addition, cryoelectron microscopy (cryo-EM) reconstructions of vir

110 in complexes obtained by crystallography and cryoelectron microscopy (cryo-EM) reveal similar interac

111 Cryoelectron microscopy (cryo-EM) showed that engagement

112 Cryoelectron microscopy (cryo-EM) single-particle analys

113 Here, we present the cryoelectron microscopy (cryo-EM) structure of a KCNQ1/c

114 Here, we present a 5.8- angstrom cryoelectron microscopy (cryo-EM) structure of EEEV comp

115 The 4 angstrom resolution cryoelectron microscopy (cryo-EM) structure of gammaTuRC

116 To close this gap, we determined the cryoelectron microscopy (cryo-EM) structure of Streptoco

117 s mutant chimera enabled us to determine the cryoelectron microscopy (cryo-EM) structure of the chann

118 A cryoelectron microscopy (cryo-EM) structure of the IRP2-

119 Here we report a 3.3- angstrom cryoelectron microscopy (cryo-EM) structure of the serot

120 Here we report cryoelectron microscopy (cryo-EM) structures of AdnAB in

121 Here, we report the cryoelectron microscopy (cryo-EM) structures of an exten

122 Here, we present cryoelectron microscopy (cryo-EM) structures of Bacillus

123 Here, we report the cryoelectron microscopy (cryo-EM) structures of Ca(v)1.1

124 Here, we determined the cryoelectron microscopy (cryo-EM) structures of chromato

125 Here, we present cryoelectron microscopy (cryo-EM) structures of DNA-boun

126 Here, we report the cryoelectron microscopy (cryo-EM) structures of DNA-PKcs

127 sent high-resolution (2.6- to 4.1- angstrom) cryoelectron microscopy (cryo-EM) structures of GII.4, G

128 Here, we present the cryoelectron microscopy (cryo-EM) structures of nanodisc

129 investigated capsid maturation by comparing cryoelectron microscopy (cryo-EM) structures of the proh

130 CRISPR-Cas system form a complex and provide cryoelectron microscopy (cryo-EM) structures of three di

131 Here, we report the cryoelectron microscopy (cryo-EM) structures of two term

132 Here, we present two cryoelectron microscopy (cryo-EM) structures of UCN1-bou

133 High-resolution cryoelectron microscopy (cryo-EM) structures reveal that

134 Cryoelectron microscopy (cryo-EM) structures reveal the

135 Recent cryoelectron microscopy (cryo-EM) studies of TRPM8 have

136 Here, we used cryoelectron microscopy (cryo-EM) to determine a substra

137 Here, we use cryoelectron microscopy (cryo-EM) to determine the quate

138 s9 genetic screens, degron assays, Hi-C, and cryoelectron microscopy (cryo-EM) to dissect the functio

139 Here we combine biochemical approaches and cryoelectron microscopy (cryo-EM) to visualize a cohesin

140 Here, we used cryoelectron microscopy (cryo-EM) to visualize the inter

141 lex bound to the nucleosome, generated using cryoelectron microscopy (cryo-EM), cross-linking mass sp

142 chaperone prefoldin/GIMc (PFD), we integrate cryoelectron microscopy (cryo-EM), crosslinking-mass-spe

143 Mimivirus genus, lineage A) as visualized by cryoelectron microscopy (cryo-EM), cryoelectron tomograp

144 on, determined to subnanometer resolution by cryoelectron microscopy (cryo-EM), showed only four prot

145 previously argued, using very low-resolution cryoelectron microscopy (cryo-EM), that C. jejuni accomm

146 Using cryoelectron microscopy (cryo-EM), we resolved the first

147 Using cryoelectron microscopy (cryo-EM), we show that KCNE3 tu

148 Using cryoelectron microscopy (cryo-EM), we show that the bind

149 calculations, and electron scattering using cryoelectron microscopy (cryo-EM).

150 n structures of human GCH1-GFRP complexes by cryoelectron microscopy (cryo-EM).

151 n microscopy (TEM), scanning TEM (STEM), and cryoelectron microscopy (cryo-EM).

152 in the ribosome-bound form against data from cryoelectron microscopy (cryo-EM).

153 termined at approximately 21-A resolution by cryoelectron microscopy (cryo-EM).

154 macromolecular 3D structure in the field of cryoelectron microscopy (cryo-EM).

155 otein synthesis at near-atomic resolution by cryoelectron microscopy (cryo-EM).

156 x with an engineered Galphaq heterotrimer by cryoelectron microscopy (cryo-EM).

157 formation and determined the structure using cryoelectron microscopy (cryo-EM).

158 and SIV Nef and determined its structure by cryoelectron microscopy (cryo-EM).

159 Cryoelectron microscopy (cryoEM) and single-particle ima

160 as determined to 13 A resolution by means of cryoelectron microscopy (cryoEM) and three-dimensional i

161 e have constructed a first-of-its-kind BSL-3 cryoelectron microscopy (cryoEM) containment facility.

162 Automatic modeling methods using cryoelectron microscopy (cryoEM) density maps as constra

163 The cryoelectron microscopy (cryoEM) image reconstruction of

164 d with ICAM-1Kilifi, have been determined by cryoelectron microscopy (cryoEM) image reconstruction to

165 rus was determined to a resolution of 6 A by cryoelectron microscopy (cryoEM) single-particle image r

166 empty wild-type particles were determined by cryoelectron microscopy (cryoEM) to 7.5-A and 11.3-A res

167 In this paper, we used cryoelectron microscopy (cryoEM) to visualize destabiliz

168 tate nuclear magnetic resonance (SSNMR), and cryoelectron microscopy (cryoEM), have enabled high-reso

169 Using gel electrophoresis and cryoelectron microscopy (cryoEM), the ability of the rec

170 osphatidylcholine vesicles, and imaged using cryoelectron microscopy (cryoEM).

171 ons of, for example, structures derived from cryoelectron microscopy data.

172 tic core that accounts for almost all of the cryoelectron microscopy density in a published map, incl

173 The structure of CsgE fits well into the cryoelectron microscopy density map of the CsgG-CsgE com

174 ctures, our new atomic model can be fit into cryoelectron microscopy density maps of the motor attach

175 e of the E1 glycoprotein was fitted into the cryoelectron microscopy density, in part by using the kn

176 lization of these peptides as bulk labels in cryoelectron microscopy-derived difference maps.

177 Cryoelectron microscopy difference maps indicated that V

178 Frank, and Richard Henderson for "developing cryoelectron microscopy for the high-resolution structur

179 Cryoelectron microscopy had shown that the tail is folde

180 Cryoelectron microscopy has recently identified the EB b

181 Recent advances in cryoelectron microscopy have accelerated structure-funct

182 ral studies with protein crystallography and cryoelectron microscopy have shed light on the residues

183 ping process based on X-ray crystallography, cryoelectron microscopy, hydrogen-deuterium exchange mas

184 4 crystal structure into a three-dimensional cryoelectron microscopy image reconstruction of the viru

185 A 5-fold symmetric, 3D reconstruction using cryoelectron microscopy images has now shown that the qu

186 In addition, cryoelectron microscopy images of actomyosin VI show the

187 rid approach combining spin labeling EPR and cryoelectron microscopy imaging at 10A resolution reveal

188 rom rabbit skeletal muscle was determined by cryoelectron microscopy in combination with homology mod

189 Here, we used cryoelectron microscopy in conjunction with electron par

190 se in the E1 state to a new 6 A structure by cryoelectron microscopy in the E2 state.

191 Images obtained from cryoelectron microscopy indicate that R120G alphaB-cryst

192 Cryoelectron microscopy indicates large conformational c

193 New results obtained by cryoelectron microscopy, interpreted in the light of x-r

194 of biochemistry, single-molecule assays, and cryoelectron microscopy-led to the surprising discovery

195 A recent cryoelectron microscopy map of Tetrahymena telomerase re

196 f component proteins into an 11-A resolution cryoelectron microscopy map.

197 Our cryoelectron microscopy maps of Hsp104 hexamers reveal s

198 Here, we present subnanometer resolution cryoelectron microscopy maps of the mammalian 80S riboso

199 l genomic 5') in vitro, and determined their cryoelectron microscopy maps to 3.3- angstrom resolution

200 Analysis of single particles in cryoelectron microscopy micrographs yields a confirmator

201 We have significantly revised the recent cryoelectron microscopy models for proteins IIIa and IX

202 Recent results obtained by cryoelectron microscopy of "naked" ribosomes and ribosom

203 Cryoelectron microscopy of 2D crystals yielded a project

204 Cryoelectron microscopy of AQP1 previously revealed the

205 Cryoelectron microscopy of cardiolipin-liposomes reveale

206 Cryoelectron microscopy of chicken granulocyte chromatin

207 Now, using cryoelectron microscopy of frozen hydrated reconstituted

208 Recently, cryoelectron microscopy of isolated macromolecular compl

209 Cryoelectron microscopy of LDL quick-frozen from 10 (cor

210 Cryoelectron microscopy of purified RyR2s showed structu

211 Cryoelectron microscopy of reconstituted AQP1 membrane c

212 Cryoelectron microscopy of RyR2 so prepared yielded imag

213 s responsible for receptor recognition using cryoelectron microscopy of the SVV-ANTXR1-Fc complex.

214 Cryoelectron microscopy of triglyceride-rich LDL prepare

215 rom co-crystals of PLB with Ca(2+)-ATPase by cryoelectron microscopy of tubular co-crystals at 8--10

216 died the structural effects of TG binding by cryoelectron microscopy of tubular crystals, which have

217 al properties of this phosphoenzyme, we used cryoelectron microscopy of two-dimensional crystals form

218 Using cryoelectron microscopy of vitreous sections, we investi

219 Using cryoelectron microscopy on ribosomes with a P-loop mutat

220 and lengths of helices from crystallography, cryoelectron microscopy, or in vivo crosslinking and che

221 er vesicles, and its direct visualization by cryoelectron microscopy pave the way for more detailed s

222 been explored with X-ray crystallography and cryoelectron microscopy procedures.

223 cture of RNA polymerase-Spt4/5 complex using cryoelectron microscopy reconstruction and single partic

224 es remarkably similar to those observed in a cryoelectron microscopy reconstruction image of a human

225 Here, we report cryoelectron microscopy reconstruction of a functional C

226 rmined to 2.2-A resolution and fitted into a cryoelectron microscopy reconstruction of a rhinovirus-I

227 A cryoelectron microscopy reconstruction of a variant of C

228 omology model of T4 Soc were fitted into the cryoelectron microscopy reconstruction of the T4 capsid.

229 pili, the F and pED208 pili, generated from cryoelectron microscopy reconstructions at 5.0 and 3.6 A

230 Here we present cryoelectron microscopy reconstructions of bacterial RNA

231 Cryoelectron microscopy reconstructions of free and DNA-

232 his study, we report subnanometer resolution cryoelectron microscopy reconstructions of microtubule-b

233 Here, we present ~3 angstrom-resolution cryoelectron microscopy reconstructions of the stator un

234 ng molecular homology modeling for Tob55 and cryoelectron microscopy reconstructions of the TOB compl

235 d fitted into approximately 8.5-A resolution cryoelectron microscopy reconstructions of the virus-rec

236 Statistical analysis of rings imaged by cryoelectron microscopy revealed 16-fold symmetry, corre

237 cursor were not affected by these mutations, cryoelectron microscopy revealed a loss of virion matura

238 Cryoelectron microscopy revealed structured termini not

239 Immunofluorescence and cryoelectron microscopy revealed that PNT1 localizes to

240 High-resolution cryoelectron microscopy revealed the protofilament bound

241 octamer complex generated by single-particle cryoelectron microscopy, revealed that several intrinsic

242 nance spectroscopy, X-ray fiber diffraction, cryoelectron microscopy, scanning transmission electron

243 Cryoelectron microscopy showed that UNC-60B changed the

244 We used cryoelectron microscopy single-particle analysis to obta

245 Here, we report the cryoelectron microscopy structure of a complex filament

246 The cryoelectron microscopy structure of ASC(PYD) filament a

247 Here we present a cryoelectron microscopy structure of human Microprocesso

248 Here, we present a cryoelectron microscopy structure of the complete 1.4-me

249 ing domain S1(A) is available and for HKU1 a cryoelectron microscopy structure of the complete S ecto

250 Here, we report a 3.7 angstrom resolution cryoelectron microscopy structure, which surprisingly re

251 Presented here are the cryoelectron microscopy structures of an MNV virion and

252 We present cryoelectron microscopy structures of Cas12a-crRNA bound

253 Three cryoelectron microscopy structures of Fab in complex wit

254 We report cryoelectron microscopy structures of full-length rat P2

255 Here, we report cryoelectron microscopy structures of human V-ATPase in

256 Here, we report the cryoelectron microscopy structures of synthetic cannabin

257 Modeling of Nas6 into cryoelectron microscopy structures of the proteasome sug

258 to solve the 3.0 and 3.1 angstrom resolution cryoelectron microscopy structures of these RNases poise

259 between VP19C and VP23 was inferred by yeast cryoelectron microscopy studies and subsequently confirm

260 Cryoelectron microscopy studies have identified distinct

261 Recent cryoelectron microscopy studies have revealed that herpe

262 Three-dimensional cryoelectron microscopy studies of Ag-Ab complexes revea

263 Previous cryoelectron microscopy studies of the mature DENV showe

264 esonance experiments on cysteine mutants and cryoelectron microscopy studies.

265 ulations, and are evident in single-particle cryoelectron microscopy studies.

266 onsistent with the predictions of a previous cryoelectron microscopy study and strongly supports the

267 Here we show, using cryoelectron microscopy, that the structure of immature

268 d crystal structures of the P dimer into the cryoelectron microscopy three-dimensional (3D) image rec

269 Cryoelectron microscopy three-dimensional reconstruction

270 Using cryoelectron microscopy, three-dimensional image reconst

271 ructurally intact by both negative stain and cryoelectron microscopy, three-dimensional reconstructio

272 Its capsid structure, determined by cryoelectron microscopy to 3- angstrom resolution, has a

273 lated, ATP-bound conformation, determined by cryoelectron microscopy to 3.4 A resolution.

274 We have used cryoelectron microscopy to characterize interactions of

275 ate its role in membrane remodeling, we used cryoelectron microscopy to characterize structural chang

276 We used cryoelectron microscopy to derive 8-9 A-resolution maps

277 We used cryoelectron microscopy to determine a 13-A resolution s

278 stability in an extreme environment, we use cryoelectron microscopy to determine the capsid structur

279 Here, we used single particle cryoelectron microscopy to determine the quaternary arra

280 We have studied this interaction by using cryoelectron microscopy to determine the structure, at 2

281 We used cryoelectron microscopy to generate a 9-A resolution thr

282 Here, we have used cryoelectron microscopy to produce an 11-A density map o

283 ty of GTP-bound FtsZ protofilaments by using cryoelectron microscopy to sample their bending fluctuat

284 We use single-particle cryoelectron microscopy to visualize seven intermediates

285 precursor could be isolated and analyzed by cryoelectron microscopy to yield a 3D structure at 22 A

286 We applied cryoelectron microscopy tomography to define ultrastruct

287 Cryoelectron microscopy was used to obtain a 3-D image a

288 Cryoelectron microscopy was used to visualize a 2-step P

289 Using cryoelectron microscopy we could localize golgin-84 to t

290 Using cryoelectron microscopy, we demonstrate that amelogenin

291 taining the alternative sigma(54) factor and cryoelectron microscopy, we determined structures of RPc

292 Using single-particle cryoelectron microscopy, we have determined the structur

293 Using cryoelectron microscopy, we present here a three-dimensi

294 Using cryoelectron microscopy, we show that although the virus

295 Utilizing small-angle X-ray scattering and cryoelectron microscopy, we underpin three crucial facto

296 anism of these transitions via time-resolved cryoelectron microscopy, whereas the predictions of prev

297 ructural data from x-ray crystallography and cryoelectron microscopy with functional measurements of

298 of these two molecules have been studied by cryoelectron microscopy, with helical crystals in the ca

299 here using a combination of single-particle cryoelectron microscopy, X-ray crystallography, NMR, and

300 y an integrative approach based on data from cryoelectron microscopy, X-ray crystallography, residue-