ライフサイエンスコーパス: electron cryomicroscopy

1 esolutions between 2.5 and 5.0 A by means of electron cryomicroscopy.

2 hree-dimensional reconstructions obtained by electron cryomicroscopy.

3 acillus stearothermophilus taken by low-dose electron cryomicroscopy.

4 d empty CPV determined at 13-A resolution by electron cryomicroscopy.

5 virus type 1 (HSV-1) B capsid, determined by electron cryomicroscopy.

6 ubiquitylated nucleosome, and validate it by electron cryomicroscopy.

7 een determined at 8.5 angstrom resolution by electron cryomicroscopy.

8 were analyzed using biochemical methods and electron cryomicroscopy.

9 the scaffolding protein have been studied by electron cryomicroscopy.

10 S)-stabilized PfAct1 filaments determined by electron cryomicroscopy.

11 of EBOV, both determined by single-particle electron cryomicroscopy.

12 tion of 3.8 A, determined by single-particle electron cryomicroscopy.

13 nward-facing conformation by single-particle electron cryomicroscopy.

14 osin at a resolution of 6.5 A, determined by electron cryomicroscopy.

15 s confidence in a structure determined using electron cryomicroscopy.

16 n15 (epsilon15) particle, by single-particle electron cryomicroscopy.

17 Here, we combined electron cryomicroscopy, 3D reconstruction, and integrat

18 implex virus type 1 virions were examined by electron cryomicroscopy, allowing the three-dimensional

19 We used electron cryomicroscopy and 3D image reconstruction to e

20 Using electron cryomicroscopy and angular reconstitution techn

21 We have used electron cryomicroscopy and angular reconstitution to vi

22 We used electron cryomicroscopy and antibody labeling to show th

23 We have used electron cryomicroscopy and computer image processing to

24 Electron cryomicroscopy and computer reconstruction reve

25 orbol-13-acetate to obtain HHV-8 capsids for electron cryomicroscopy and computer reconstruction.

26 nd inside constricting liposomes by means of electron cryomicroscopy and cryotomography.

27 plied X-ray crystallography, single-particle electron cryomicroscopy and electrophysiology to rat NMD

28 We have used electron cryomicroscopy and helical reconstruction to id

29 We have used electron cryomicroscopy and helical reconstruction to id

30 construction of G2-6:F-actin was obtained by electron cryomicroscopy and helical reconstruction.

31 gal partitivirus, determined in this case by electron cryomicroscopy and homology modeling.

32 We used electron cryomicroscopy and icosahedral image analysis t

33 In this study, we used transmission electron cryomicroscopy and icosahedral image reconstruc

34 Using electron cryomicroscopy and icosahedral image reconstruc

35 Electron cryomicroscopy and icosahedral reconstruction a

36 Using electron cryomicroscopy and icosahedral reconstruction o

37 Recent developments in electron cryomicroscopy and image analysis have made it

38 Electron cryomicroscopy and image analysis of New World

39 id isolated from VEEV has been determined by electron cryomicroscopy and image reconstruction and rep

40 Examination of the VLPs by electron cryomicroscopy and image reconstruction at 15.4

41 e was determined to 12-A resolution by using electron cryomicroscopy and image reconstruction techniq

42 We used electron cryomicroscopy and image reconstruction to dete

43 erminus of VP2 within the core, we have used electron cryomicroscopy and image reconstruction to dete

44 We have used electron cryomicroscopy and image reconstruction to obta

45 e 25-A structure of VEE virus, obtained from electron cryomicroscopy and image reconstruction.

46 d barrel clathrin coat at 21 A resolution by electron cryomicroscopy and of the clathrin terminal dom

47 atelet integrin alpha(IIb)beta(3) derived by electron cryomicroscopy and single particle image recons

48 annel (also known as RyR1) was determined by electron cryomicroscopy and single particle reconstructi

49 ith an ATP-ADP mixture at 11 A resolution by electron cryomicroscopy and single-particle averaging of

50 ion of human fatty acid synthase obtained by electron cryomicroscopy and single-particle image proces

51 -density lipoprotein (LDL) was obtained from electron cryomicroscopy and single-particle image recons

52 te receptor (InsP3R1) has been determined by electron cryomicroscopy and single-particle reconstructi

53 By the use of electron cryomicroscopy and single-particle reconstructi

54 We have used electron cryomicroscopy and three-dimensional image reco

55 We used electron cryomicroscopy and three-dimensional image reco

56 o directly locate the KSHV SCP, we have used electron cryomicroscopy and three-dimensional reconstruc

57 ime allowing direct structure comparisons by electron cryomicroscopy and three-dimensional reconstruc

58 Electron cryomicroscopy and three-dimensional reconstruc

59 protein (FKBP12), have been characterized by electron cryomicroscopy and three-dimensional reconstruc

60 structures of Tula hantavirus virions using electron cryomicroscopy and tomography.

61 process, consistent with recent models from electron cryomicroscopy and X-ray crystallography.

62 of DNA packing in HCMV and HSV-1 virions by electron-cryomicroscopy and image processing.

63 ng time-resolved phosphorescence anisotropy, electron cryomicroscopy, and all-atom molecular dynamics

64 We used a combination of bioinformatics, electron cryomicroscopy, and biochemical techniques to i

65 Here we demonstrate using genomic analysis, electron cryomicroscopy, and image reconstruction that t

66 n, quantitative agarose gel electrophoresis, electron cryomicroscopy, and nuclease digestion.

67 mensional crystals of CydDC were analyzed by electron cryomicroscopy, and the protein was shown to be

68 these structures, X-ray crystallography and electron cryomicroscopy are capable of determining struc

69 we are now firmly within the "atomic age" of electron cryomicroscopy, as these studies can reveal ato

70 Furthermore, by using electron cryomicroscopy, as well as penton- and protein

71 type 1 RyR (RyR1), solved by single-particle electron cryomicroscopy at an overall resolution of 4.8

72 formed by Abeta(1-40) peptide, determined by electron cryomicroscopy at approximately 8-A resolution.

73 ) supercomplex determined by single-particle electron cryomicroscopy at near-atomic to sub-nanometre

74 n of the Pr-minus and wild-type B capsids by electron cryomicroscopy, at an unprecedented 12.5-angstr

75 These observations support an electron cryomicroscopy-based structural model on which

76 res of many proteins cannot be determined by electron cryomicroscopy because the individual proteins

77 Electron cryomicroscopy can yield near-atomic resolution

78 biochemical reconstitutions, single-particle electron cryomicroscopy, cross-linking mass spectrometry

79 mbrane protein complex have been analysed by electron cryomicroscopy (cryo EM).

80 We report here single particle electron cryomicroscopy (cryo-EM) analysis of the bovine

81 A protease with its transmembrane domains by electron cryomicroscopy (cryo-EM) and atomic structure f

82 We used electron cryomicroscopy (cryo-EM) and image analysis to

83 Recently published electron cryomicroscopy (cryo-EM) and X-ray crystallogra

84 omer boundaries in a subnanometer-resolution electron cryomicroscopy (cryo-EM) density map.

85 large high-symmetry viruses, single-particle electron cryomicroscopy (cryo-EM) has achieved the deter

86 Electron cryomicroscopy (cryo-EM) has been used to deter

87 Here, we present electron cryomicroscopy (cryo-EM) maps showing that VAT

88 Here we report the electron cryomicroscopy (cryo-EM) reconstruction of the

89 We have used electron cryomicroscopy (cryo-EM) to examine the filamen

90 captured images of this transient process by electron cryomicroscopy (cryo-EM) to reveal the structur

91 Using electron cryomicroscopy (cryo-EM) we have structurally c

92 ormed mass-per-length (MPL) measurements and electron cryomicroscopy (cryo-EM) with 3D reconstruction

93 Electron cryomicroscopy (cryo-EM) yields images of macro

94 microscopy of cryogenically cooled samples (electron cryomicroscopy (cryo-EM)).

95 The structures were determined using electron cryomicroscopy (cryo-EM), and the three-dimensi

96 With single-particle electron cryomicroscopy (cryo-EM), it is possible to vis

97 Using electron cryomicroscopy (cryo-EM), we present a reconstr

98 ngle-particle analysis of images obtained by electron cryomicroscopy (cryo-EM).

99 uman CFTR without nucleotides, determined by electron cryomicroscopy (cryo-EM).

100 infectious rotavirus particle determined by electron cryomicroscopy (cryoEM) and single-particle ana

101 FcRY's pH-dependent binding mechanism using electron cryomicroscopy (cryoEM) and small-angle X-ray s

102 r Epinephelus malabaricus, was determined by electron cryomicroscopy (cryoEM) and three-dimensional r

103 f antigen-antibody complexes.Single-particle electron cryomicroscopy (cryoEM) can circumvent some of

104 Complementing this work, electron cryomicroscopy (cryoEM) has provided relatively

105 We have combined image reconstructions from electron cryomicroscopy (cryoEM) of bovine papillomaviru

106 We report here low-resolution (20 A) electron cryomicroscopy (cryoEM) structures of this gp14

107 We have determined by electron cryomicroscopy (cryoEM), at about 11 A resoluti

108 ific structural information that complements electron cryomicroscopy data and defines targets and str

109 e for near-atomic to high-resolution (3-5 A) electron cryomicroscopy data evaluation.

110 Fitting of the modeled PapA subunit into the electron cryomicroscopy data provides a detailed view of

111 procapsid and infectious virion derived from electron cryomicroscopy density maps determined at 3.8-

112 to the previously determined 25-A-resolution electron cryomicroscopy density maps of HAstV allowed us

113 the truncated E2 core, using low-resolution electron cryomicroscopy density maps.

114 igh-resolution, all-atom protein models from electron cryomicroscopy density maps.

115 s complex I, determined to 5-A resolution by electron cryomicroscopy, described the structure of the

116 Using electron cryomicroscopy difference mapping, we have iden

117 study, we analyzed E1HT by a combination of electron cryomicroscopy, electron crystallography of neg

118 of TRPV1 determined by using single-particle electron cryomicroscopy exhibits fourfold symmetry and c

119 rus structure and reflect the growing use of electron cryomicroscopy for atomic modeling of protein f

120 nd to F-actin, highlighting the potential of electron cryomicroscopy for structure-based drug design.

121 Electron cryomicroscopy had previously given detailed ri

122 Advances in single-particle electron cryomicroscopy have recently revealed details o

123 des and phases can be computed directly from electron cryomicroscopy images.

124 ted mutagenesis, ultrastructural analysis by electron cryomicroscopy, immunocytochemistry, and molecu

125 To this end we have used single-particle electron cryomicroscopy in combination with cross-linkin

126 Electron cryomicroscopy in conjunction with single-parti

127 Here, we provide evidence, using electron cryomicroscopy, in conjunction with light-scatt

128 e of the alpha(V)beta(3) ectodomain into the electron cryomicroscopy map of alpha(IIb)beta(3) require

129 An electron cryomicroscopy map of PsV-F shows that the diso

130 nt and its modeling into an 8.5 A resolution electron cryomicroscopy map of the HSV-1 capsid.

131 e, allowing us to obtain a ~3.9-A resolution electron cryomicroscopy map of the VO complex and build

132 no acid side chains were identified from the electron cryomicroscopy map.

133 rgent dodecyl maltoside, which is visible in electron cryomicroscopy maps.

134 Here, using modern electron cryomicroscopy methods, we investigate the stru

135 Utilizing novel electron cryomicroscopy methods, we solved structures of

136 ion images of assembled coats, determined by electron cryomicroscopy, now provide the information nec

137 cherichia coli multidrug transporter EmrE by electron cryomicroscopy of 2D crystals, including data t

138 ce at subnanometre resolution, obtained from electron cryomicroscopy of coats assembled in vitro.

139 Here, using electron cryomicroscopy of EmrE two-dimensional crystals

140 Electron cryomicroscopy of rotor complexes of the Salmon

141 Electron cryomicroscopy of S1-bound actin filaments, tog

142 luenza neuraminidase, has been determined by electron cryomicroscopy of single particles and image an

143 synthase at approximately 18 A resolution by electron cryomicroscopy of single particles in amorphous

144 P synthase from bovine heart mitochondria by electron cryomicroscopy of single particles.

145 ly 12 A resolution image reconstruction from electron cryomicroscopy of trypsin-primed virions shows

146 ed in icosahedral image reconstructions from electron cryomicroscopy of trypsinized rotavirus virions

147 eromyosin suitable for structural studies by electron cryomicroscopy of unstained, frozen-hydrated sp

148 e here a structure at 3.9 A resolution, from electron cryomicroscopy, of Pepino mosaic virus (PepMV),

149 ation of the envelope glycoprotein either by electron cryomicroscopy or X-ray crystallography.

150 sualized the double-layered COPII coat using electron cryomicroscopy, providing insight into how coat

151 In this work, we show the electron cryomicroscopy reconstruction of a bacterial dy

152 Here we present the electron cryomicroscopy reconstruction of an ATP-activat

153 , determined by fitting the subunit into the electron cryomicroscopy reconstruction of the virus, ide

154 e cleavage site, did not mature at pH 5, and electron cryomicroscopy reconstruction showed that it wa

155 Here, we present electron cryomicroscopy reconstructions of dodecameric y

156 Here we present the 3D electron cryomicroscopy reconstructions of the major Ufd

157 were clearly visible and well ordered in the electron cryomicroscopy reconstructions of TR TLPs, they

158 Using the low-resolution maps from electron cryomicroscopy reconstructions, the simulations

159 cofilactin filament structures determined by electron cryomicroscopy reveal how cofilin enhances the

160 FTCD structure by X-ray crystallography and electron cryomicroscopy revealed that the eight subunits

161 Electron cryomicroscopy revealed two major particle popu

162 Analysis by electron cryomicroscopy reveals a triangular shaped olig

163 The virion structure, determined by electron cryomicroscopy, reveals that the bulk of the ou

164 ensional structures of full and empty CPV by electron cryomicroscopy show identical outer shells but

165 Both conventional and electron cryomicroscopy showed clearly that the ribbons

166 High resolution electron cryomicroscopy showed that one such peptide bin

167 Three-dimensional structural studies using electron cryomicroscopy showed that the binding of one F

168 Our approach combines electron cryomicroscopy, site-directed mutagenesis, homo

169 rientation distribution of a single-particle electron cryomicroscopy specimen limits the resolution o

170 s has been determined to 3.4 A, using a 22-A electron cryomicroscopy structure as a phasing model.

171 describe a 4.2-A resolution single-particle electron cryomicroscopy structure of complex I from Bos

172 re, we report a 3.6-A helical reconstruction electron cryomicroscopy structure of four-stranded mini

173 Here, we improved upon our previous electron cryomicroscopy structure of Salmonella bacterio

174 ur knowledge, near-atomic (4.7 A) resolution electron cryomicroscopy structure of the tetrameric mamm

175 nal and visualization analysis from the 8.5A electron cryomicroscopy structure of the whole capsid.

176 Our mutational analysis, based on the electron cryomicroscopy structures of monomeric Pol I al

177 virions, the available crystallographic and electron cryomicroscopy structures of NV have not reveal

178 P22 coat protein lattice, we have determined electron cryomicroscopy structures of scaffolding-contai

179 We have determined by electron cryomicroscopy the structure of the vesicular s

180 tif with nanogold and used three-dimensional electron cryomicroscopy to compare images of microtubule

181 Here, we have used electron cryomicroscopy to determine 12-A-resolution str

182 We used electron cryomicroscopy to determine structures of ArfA

183 hannel called "portal protein." We have used electron cryomicroscopy to determine the structure of ba

184 Here we use electron cryomicroscopy to determine the structure of th

185 We have used electron cryomicroscopy to determine the structures of r

186 emerging technique of Zernike phase-contrast electron cryomicroscopy to enhance the image contrast of

187 We have used three-dimensional electron cryomicroscopy to gain insight into the structu

188 tional constraints from linear dichroism and electron cryomicroscopy to obtain the allowed orientatio

189 Here we use electron cryomicroscopy to solve the structure of the co

190 We have used single-particle electron cryomicroscopy to study the multilayer structur

191 We have used electron cryomicroscopy to study tubular particles extra

192 Here we used electron cryomicroscopy together with computer-based doc

193 Here, electron cryomicroscopy together with computer-based doc

194 A three-dimensional reconstruction from electron cryomicroscopy was used as a molecular replacem

195 Using electron cryomicroscopy, we calculated difference maps b

196 Using electron cryomicroscopy, we determined a 3.5-angstrom-re

197 Using electron cryomicroscopy, we determined the molecular str

198 Using electron cryomicroscopy, we determined the three-dimensi

199 Here, using electron cryomicroscopy, we have determined the structur

200 Using electron cryomicroscopy, we have determined the three-di

201 By using recent advances in single-particle electron cryomicroscopy, we have solved the structure of

202 Using electron cryomicroscopy, we present reconstructions of f

203 to a reconstruction of the whole virion from electron cryomicroscopy, we propose that each sigma3 sub

204 Also using electron cryomicroscopy, we reconstruct ParM doublets fo

205 d fully defined chromatin arrays obtained by electron cryomicroscopy, we report a linker histone-depe

206 Using electron cryomicroscopy, we show here that ATP binding o

207 ined under various chemical conditions using electron cryomicroscopy, we show here that the viral gen

208 Subsequent single-particle electron cryomicroscopy yielded a reconstruction at appr