ライフサイエンスコーパス: packing

1 the rate of fluid flow through the granular packing.

2 self-generated pumping of fluid through the packing.

3 a kink at TM12 preventing favorable monomer packing.

4 the local lateral density of lipids or lipid packing.

5 with different properties such as charge or packing.

6 if the columns aggregate in a hexagonal rod packing.

7 to be correlated with the color and crystal packing.

8 nsidered in clusters with various degrees of packing.

9 ensity estimated to be in the range of close packing.

10 entation, after post-fermentation, and after packing.

11 blocks can lead to large changes in crystal packing.

12 via inverse jamming and topographical close-packing.

13 t nonnative effect is not observed for H1-H4 packing.

14 ly dependent on fullerene aggregate size and packing.

15 le differences in intramolecular helix-helix packing.

16 ore variable physical dimensions with looser packing.

17 light absorption and stronger intermolecular packing.

18 nds of bull protamine results in tighter DNA packing.

19 erimentally observed antiparallel beta-sheet packing.

20 bers' microscopic polymer chain relaxing and packing.

21 in size and topology of their alpha-helical packing.

22 y of PSS standards and changes in the column packing.

23 degree of isotropic character in the crystal packing.

24 unctionalization of cysteines results in AB2 packing.

25 s valuable insights on how to create all-ftf packings.

26 tructure and statistical descriptors of such packings.

27 originated from the use of therapeutic liver packing, a practice that had previously been abandoned a

28 ntiparallel beta-sheets with 7 main strands, packing against each other, forming a beta-sandwich.

29 oride salt of CFZ (CFZ-HCl)-has a corrugated packing along the (001) face and weak dispersive bonding

30 Here we probe how the crystal packing alters microsecond dynamics, using solid-state N

31 r dynamics simulations and show that crystal packing alters the thermodynamics and kinetics of local

32 Based on a crystal packing analysis that was performed on crystals of NFeoB

33 substitutions at position 2 aided in tighter packing and activity, and the ring type and size of ring

34 r results illustrate the unification of core packing and binding-site definition as a central princip

35 region of FtsLB is stabilized by hydrophobic packing and by a complex network of hydrogen bonds.

36 ich show that a combination of van der Waals packing and Calpha-H hydrogen bonding predicts the exper

37 end, which we propose to play a role in DNA packing and delivery.

38 anic framework (MOF), which after successful packing and densification reaches 259 cm(3) (STP) cm(-3)

39 text], a uniformity similar to random close packing and early universe fluctuations, but with arbitr

40 y and thus can better maintain its molecular packing and electron mobility in the blend.

41 sequences of their incorporation on membrane packing and endothelial cell stiffness.

42 g the total metabolites content, were vacuum packing and freezing for intermediary storage times (24-

43 saturation is a key factor determining lipid packing and membrane fluidity, and it must be tightly co

44 l, and a large Chol-driven increase in lipid packing and membrane surface charge density.

45 In addition, they modulated lipid packing and miscibility of laterally segregated liquid d

46 Polycomb-repressed domains show the densest packing and most intriguing chromatin folding behaviour,

47 wisting bundles that break the symmetries of packing and of the underlying inter-filament forces, par

48 te structures critical for their solid-state packing and optoelectronic properties.

49 lar sheet requires stringent control of cell packing and organization.

50 tions to design PfRH5 variants with improved packing and surface polarity.

51 rticipate in stabilizing the trimer-of-dimer packing and the kinase-ON state of core signaling comple

52 ree different environments in soil aggregate packings and monitored contaminant exchange dynamics bet

53 many of the steps of cell infection, genome packing, and cell-to-cell as well as host-to-host transf

54 ne substitution on main-chain conformations, packing, and electronic couplings are examined.

55 lipids on model bilayer properties, membrane packing, and endothelial cell biomechanics was investiga

56 with collagen affect collagen cross-linking, packing, and fibril diameter.

57 polymer structural conformation, nanocrystal packing, and superlattice dimensions.

58 distances, narrower crossing angles, better packing, and the formation of larger networks of Calpha-

59 r "walking" on an actin fibre, RNA stem-loop packing, and the simulation of cell motion and aggregati

60 quential addition algorithm to generate such packings, and have computed a variety of microstructural

61 Small-residue-mediated interhelical packings are ubiquitously found in helical membrane prot

62 deuterium mass spectrometry revealed altered packing arrangements of beta-sheets that encompass resid

63 the dimensionality and directionality of the packing arrangements on charge transport in organic semi

64 terials that typically exhibit high-symmetry packing arrangements, which optimize the interactions be

65 can adopt multiple conformations and diverse packing arrangements.

66 l protein segment dynamics, and interprotein packing as a function of aggregation time, along the thi

67 ECN1 helical region that transitions between packing as part of either one of two conserved domains (

68 ation of the related Frank-Kasper A15 sphere packing as well as a common body-centered cubic structur

69 tal processes such as epithelial geometrical packing as well as generation of forces required for bla

70 result in favorable changes to the molecular packing behaviors of the acceptor and improved morpholog

71 lateral lipid diffusion and increases lipid packing beneath the alphaS clusters.

72 lustrate that the GXXXG motif controls helix packing but still allows for a dynamic and lipid-regulat

73 lipid mixtures are shown to adopt a compact packing by offsetting the positioning depths at which di

74 iation between face-to-face and edge-to-edge packing by tailoring the size of DNA nanostructures.

75 serted cations expand the parent herringbone packings by reorienting the molecular anions to create m

76 er of nearest neighbor clusters in colloidal packings by statistically analyzing the angular correlat

77 embranes; conversely, lipid conformation and packing can adapt to the presence of peptides.

78 vel packing motifs and determine whether the packing can be steered into a desired direction, so to a

79 Herein we show, that crystal packing can completely overrule the relative stabilities

80 families, which have shown that mirror-image packing can enable opposite enantiomers to be accommodat

81 visual receptor rhodopsin, whereas sites in packing cluster 1 (e.g., positions 1.46 and 2.47) are mo

82 ved small side chain at position 4.53 within packing cluster 2 is shown to disrupt the structure of t

83 We introduce a parameter-the packing coefficient Pc, which gives an estimate of the d

84 The science of packing columns with stationary phases is one of the mos

85 ay diffraction analysis and the C18 columnar packing compared in a systematic manner.

86 icity arises largely from buried hydrophobic packing complemented by irregular peripheral polar inter

87 lar material can include different molecular packing configurations that differ in stability and func

88 stallographic data, and suggest that crystal packing contacts trap the RNA in an inactive conformatio

89 truncated tails, including decreased bilayer packing, decreased bilayer bending modulus, and increase

90 oxygen-packing fraction, showing that oxygen packing decreases at ultrahigh pressures to accommodate

91 bilayers, and it strongly affects both lipid-packing defects and the lateral pressure profile.

92 Low packing densities are key structural features of amphidy

93 lated bull nuclei achieve slightly lower DNA packing densities compared to salmon nuclei despite salm

94 photonic integrated circuits with ultra-high packing densities.

95 hs to achieve structural compaction and high packing densities.

96 mation and interaction parameters, including packing density and residue depth.

97 The nanostructure not only improves the packing density and the proper orientation of the IgG, b

98 omatin folding behaviour, in which chromatin packing density increases with domain length.

99 While the packing density model, and to a higher degree, the pathw

100 Achieving a high packing density of coils in the lumen of aneurysms can d

101 st challenging approaches for increasing the packing density of photonic integrated circuits.

102 rature, based on Yukawa potential in the low packing density regime.

103 s 3 typical packing patterns and relates the packing density to the aspect ratio.

104 rtance of considering antibiotic loading and packing density when investigating the clinical applicat

105 ariation of the nanoparticle shape and size, packing density, flow conditions, and analyte diffusivit

106 This fundamentally limits their packing density.

107 40, and E42, due to solvent exposure and low packing density.

108 d structure evolution of proteins with lower packing density.

109 However, in the liquid state, in which this packing difference is not obvious, it seems natural to a

110 atin proteins carry out essential functions: packing DNA during cell division, partitioning DNA into

111 DNA repair proteins and modulating chromatin packing during processing of the damaged DNA template.

112 sic feature of the molecule and that crystal packing effects have only a minor influence.

113 tions suggest that in the absence of crystal packing effects, the EPOR chains in the different dimers

114 sensitivity towards collective intercolumnar packing effects.

115 A at 0 K) and emphasize the significance of packing effects; the gas-phase dimer structure at the sa

116 bed molecules increases, and the geometrical packing efficiency is constrained.

117 associations between PSI primarily maximize packing efficiency; short-range interactions with Comple

118 alent counterions to temporarily perturb the packing features of the ionic groups in a homopolymer, w

119 evalence of food allergies and the intake of packing foods in the past two decades urge the need for

120 Crystal-packing forces can have a significant impact on the rela

121 strates that when optimized, hydrophobic and packing forces may be used to replace the complementary

122 The UBPs form based on hydrophobic and packing forces, as opposed to complementary hydrogen bon

123 on proceeds without a detectable increase in packing fraction, and imaging the evolving flow field we

124 oncile the changes in relation to the oxygen-packing fraction, showing that oxygen packing decreases

125 round state order in the dispersion at lower packing fractions.

126 ed to investigate three filler materials for packing fungus biofilm.

127 stituents yield four distinct intermolecular packing geometries, resulting in variable intermolecular

128 vel extendable loop may help ameliorate poor packing geometry of the rigid main particle at the angle

129 ile actin filaments and perturbed epithelial packing geometry.

130 at can ultimately be programmed by molecular packing geometry.

131 no flow control, dye injected on top of the packing gets drawn into the grains.

132 ype of crystallization, and thus the crystal packing, has no impact on anisotropy, nor does the natur

133 red-cubic (fcc) structure to hexagonal-close-packing (hcp) structure in the prototype CoCrFeMnNi high

134 apatite precursors to confer even nanodopant packing, improving therapeutic outcomes in bone repair b

135 ormation and hence highly ordered interchain packing in aggregates.

136 Manzanilla cultivar, and also as a result of packing in all three cultivars.

137 ntal utility of families of solutions to the packing in confinement problem.

138 rprisingly, the ordered and close interchain packing in F-P3EHT does not lead to strong excitonic cou

139 domains use proline motifs to create optimal packing in homotrimer assembly distinct from classical t

140 , in contrast to the favored nonnative H1-H2 packing in isolation, the native H1-H2 packing orientati

141 revious work has demonstrated that molecular packing in organic crystals can strongly influence photo

142 Frustration is detected in H1-H2 packing in that a nonnative packing orientation is signi

143 he amorphous carbon units of biochar and C60 packing in the nC60 superstructure.

144 , resulting in tight and loose axial subunit packing in the rod and hook, respectively, conferring th

145 latter also crucially directs the molecular packing in the solid.

146 The cohesion and packing in the structures of HAB aggregates induce effec

147 The optimal AuNP packing in the wall, moderated by the custom ligands and

148 Genome packing in viruses and prokaryotes relies on positively

149 idine, in particular, on the dynamics of DNA packing, increases with decreasing packing velocities.

150 tions spanning several microseconds of dsDNA packing inside nanometer-sized viral capsids.

151 Aromatic packing interactions were completely lost, although hydr

152 the inhibitory helix without perturbing its packing interactions with the ETS domain.

153 the hydrophobic surface of A2AR, increasing packing interactions within the receptor and stiffening

154 n close proximity to each other via aromatic packing interactions, whereas the positively charged res

155 ifferent C-X...NR3 (X = I, Br) distances and packing interactions.

156 aortic lumen expansion as well as epithelial packing into hexagonal shapes are controlled.

157 vely conserved across all sub-regions, PSD95 packing into nanoclusters also varied between sub-region

158 rfaces; in contrast to 3D where heterochiral packing is more common.

159 presence of those perturbations, icosahedral packing is not the most stable arrangement for a wide ra

160 The current hypothesis is that homochiral packing is preferred on surfaces; in contrast to 3D wher

161 perturbation of charge, hydrogen bonding, or packing, likely affecting the temperature-dependent flex

162 eveal any immediate changes in local protein packing, local conformations and local protein dynamics

163 gest further that nonnative effects in H1-H2 packing may be largely avoided by the experimentally inf

164 This packing mechanism affects the area per lipid, the bilaye

165 ral proteins typically relies on hydrophobic packing, metal binding, or disulfide bond formation in t

166 orphologies of natural higher-order collagen packing might be rooted in the characteristic deformatio

167 x rotations and movements toward a two-helix packing mode.

168 Experiments combined with ellipsoid packing models revealed that the mechanosensitivity of c

169 In light of these observations, sphere close packing models were explored.

170 shown to organize into novel tunable surface packing morphologies on the micrometer scale.

171 red Im9 folding transition state with native packing most developed at the H1-H4 rather than the H1-H

172 geometric frustration of a locally preferred packing motif leads to anomalous behaviours, from self-l

173 nanoconfined space adopts a lattice-strained packing motif of the NWs for strong intermolecular elect

174 f this cyclophane reveals a herringbone-type packing motif, leading to two types of pi...pi interacti

175 ts a lattice-strained and single-crystalline packing motif, which can be harnessed for strong intermo

176 vior of 3 was extensively studied to unravel packing motifs and determine whether the packing can be

177 tures of the molecules and their solid-state packing motifs have been determined by X-ray crystallogr

178 for the most common energetically favorable packing motifs in crystalline structures.

179 motifs are in turn compared to the observed packing motifs in the actual liquid or glass structures

180 tatistical potential derived from side-chain packing, named OPUS-DOSP, for protein structure modeling

181 tate and the characterization of the crystal packing of a Br-substituted Biginelli-like derivative, w

182 mainly attributed to the more ordered pi-pi packing of acceptor aggregates, higher domain purity and

183 ntly active "agitator" that destabilizes the packing of adjacent residues, causing a domino chain of

184 l atomic-level structure associated with the packing of all atoms or solute-centered clusters.

185 e two kinetic intermediates is structure and packing of alpha-helices 3 and 7 and the degree of struc

186 For efficient bacteria capture, on-the-spot packing of antibody-functionalized microbeads was comple

187 percooled liquids, involving a change in the packing of atomic clusters over medium-range length scal

188 ffect, as a result of the ordering and dense packing of AuNPs and MNPs in the membrane.

189 his material has a geometry similar to a wet packing of beads, but with an additional control over th

190 anization of subunit interface, altering the packing of beta-sheets to induce changes that lead to as

191 ating that POVPC and PGPC decrease the lipid packing of both ordered and disordered membrane domains.

192 This strategy of shape-directed packing of chains of microporous polymers may be applied

193 e system results in hierarchical sorting and packing of clusters.

194 The macroscopic packing of CO2 in the pores is directly influenced by th

195 An analysis of the interior packing of family A GPCR crystal structures reveals two

196 re of the ASR trimer revealed a more compact packing of helices and side chains at the intermonomer i

197 mines the thickness of the nanosheet and the packing of helices defines the presence of nanoscale cha

198 d interaction across multiple length-scales: packing of hydrophobic proteins and folding into seconda

199 ic resolution, leading to a highly efficient packing of I2 molecules with an exceptional I2 storage d

200 microporosity is generated from the awkward packing of its 2D polymer chains in a 3D amorphous solid

201 at two salt concentrations confirm the close packing of lipid around of the stably inserted DNA pore

202 silica nanoparticles occurs via irreversible packing of micelles with non-uniform size distribution.

203 before transitioning to a phase dominated by packing of morphological space.

204 e thick filament is characterized by helical packing of most of the myosin head or motor domains on t

205 vidual molecules in live cells is limited by packing of multiple copies of labeled molecules within t

206 f CD82 glycosylation increases the molecular packing of N-cadherin and promotes the bone marrow homin

207 composed of face-centered cubic (fcc) close-packing of near-spherical C60 superatoms.

208 at this behavior reflects the more favorable packing of oleates compared to branched carboxylates on

209 resented results support the hypothesis that packing of peptide hormones/neuropeptides in dense-core

210 cular mechanisms of amyloid formation during packing of peptides into secretory vesicles and amyloid

211 visualized the native arrangement and dense packing of photosystem I (PSI), photosystem II (PSII), a

212 ical cage, focusing on the regularity of the packing of protein-like objects on the surface.

213 The helix bundle binds gRNA, causing denser packing of RNA in its proximity, which asymmetrically ex

214 ure is a common feature of amyloids, but the packing of sheets against one another is distinctive rel

215 Herein, the selective recognition and dense packing of SO2 clusters through multiple synergistic hos

216 l constraints and resulted from an efficient packing of the cochlear duct within the petrous bone.

217 Although the packing of the conjugated chains in the solid state is k

218 XRD assays showed that the overall molecular packing of the conjugates is organized according to a he

219 ons and as a result of the altered molecular packing of the crystals, exhibits significant changes to

220 that the two peptides adopt distinct lateral packing of the diffracting units.

221 structure of apo-PS1 retains the remote core packing of the holoprotein, with a flexible binding regi

222 ed mates) at this interface adjust to enable packing of the hydrophobic iodine atoms within the core

223 misdirected flow and disrupts the hexagonal packing of the ingressing furrows.

224 cholesterol was shown to disrupt the regular packing of the lbeta state.

225 ding stage largely stabilized by a favorable packing of the ligand's apolar moieties with the hCAII "

226 Tight packing of the major virion glycoprotein (VP1) is ensure

227 mpact of mutating four residues that mediate packing of the OH against both the CCD and BARAD on stru

228 ikely because of the resulting tighter chain packing of the phospholipids, which reduces the capacity

229 experiments and simulations reveal that the packing of the protein can significantly alter the therm

230 (+) not only affects the overall solid-state packing of the Th-nitrato complexes but also influences

231 tal measurement we find that the inefficient packing of the two-dimensional (2D) chains of PIM-TMN-Tr

232 scattering (SAXS) pattern shows the periodic packing of the ultrathin NWs along the radial direction,

233 helix kinks are indispensable for the tight packing of transmembrane (TM) helices.

234 The constrained packing of triangular binding footprints of truncated te

235 bundles cannot be attributed to the specific packing of triple helices in the fibril core.

236 suggest that the different sizes and enzyme packings of alpha- and beta-carboxysomes each constitute

237 stal benzene monomer into single-crystalline packings of carbon nanothreads, a one-dimensional sp(3)

238 balls" in a liquid, in analogy with regular packings of macroscopic spheres.

239 detailed simulation and characterization of packings of non-overlapping cubic particles.

240 e commonality in their values for disordered packings of objects ranging from atoms to grains, spanni

241 olecular monomers to form single-crystalline packings of polymers, threads, and higher dimensional ca

242 The authentication of packing oil from commercial canned tuna and other tuna-l

243 apes, sizes, lattice parameters, and cluster packing on both supports, while x-ray photoelectron and

244 raction was identified as a force in crystal packing or in the formation of supramolecular chains.

245 traints on protein evolution such as residue packing or solvent accessibility.

246 andom networks of point-atoms, random sphere packings, or simple crystal lattices; all of these model

247 Dynamic heterogeneities in packing order were detected in mixed-lipid bilayers.

248 thelium that undergoes a gradual increase in packing order, without concomitant large-scale changes i

249 ence and absence of heterogeneities in lipid-packing order.

250 etected in H1-H2 packing in that a nonnative packing orientation is significantly stabilized relative

251 H1-H2 packing in isolation, the native H1-H2 packing orientation is stabilized by H3 and loop residue

252 fibrinogen gamma' showed reduced protofibril packing over a range of thrombin concentrations.

253 f motifs, that progressively favor tile-tile packing over duplex-end pi-stacking.

254 ock, which in turn causes a reduction in the packing parameter and hence induces a vesicle-to-worm (o

255 of the stabilizer block and so reducing the packing parameter for the copolymer chains.

256 a mesoscopic C-S-H model, reveals 3 typical packing patterns and relates the packing density to the

257 The observation for the dense packing planes of NCs in fast growing fcc rather than bc

258 unding, geometric cues imposed by tight cell packing prevail and cells divide along their long apical

259 sponding isoforms by solving a series of bin-packing problems.

260 Phenomenologically, the column packing process can be considered as a constant pressure

261 The column packing process can be treated as science whose unified

262 theoretical mean-torque model provides acyl-packing profiles representing the cumulative chain exten

263 This packing results in the formation of colossal icosidodeca

264 important quality assurance procedures; (3) packing samples correctly requires careful training and

265 al lattice in contrast to the typical type I packing seen from membrane protein structures crystalliz

266 olgi resembles that of the amphipathic lipid-packing sensor (ALPS) motif of GMAP-210: both preferred

267 ilaments differ in their inter-protofilament packing, showing that they are ultrastructural polymorph

268 nuate the register mismatch and enhance HAMP packing stability, leading to a kinase-off output respon

269 sult of the post-fermentation and subsequent packing stage were explored by solid phase micro-extract

270 changes because of the post-fermentation and packing stages.

271 e OH transitions between these two different packing states, with the predominant state comprising th

272 ture, focusing on the two opposite limits of packings (strong excluded-volume) and networks (no exclu

273 r the presence of quantum-beating signals by packing structurally flexible synthetic heterodimers on

274 ition processing) influences the solid-state packing structure and thus the mechanical properties.

275 diffraction analysis confirmed a low-density packing structure consisting of one molecule of 2 and ap

276 long-standing debate over fractal models of packing structure in metallic glasses (MGs).

277 gle of the Fc unit which in turn affects the packing structure of the molecular diodes.

278 stronger molecular aggregation, more ordered packing structure, thus over one order of magnitude high

279 are associated with local changes in polymer packing that may impede ion transport to different exten

280 ults from rearrangements to hydrophobic core packing that modify its structure.

281 The theory predicts that, in packings, the local orientational order due to excluded-

282 sybII impose sterical restraints on oligomer packing, thereby maintaining an appropriate plasticity a

283 wchart, a logical approach to optimal column packing, thus eliminating the trial and error approach c

284 he context of BN-9,1-Naph can impact crystal packing to favor a cofacial pi-stack motif.

285 ew parameter correlates strongly with atomic packing topology, and also with the activation energy fo

286 local hydration, fluidity, and lateral lipid packing, usually characterized by the generalized polari

287 er, a small increase in the heterogeneity of packing velocities was observed in the systems with magn

288 cs of DNA packing, increases with decreasing packing velocities.

289 These effects result in an increase in the packing velocity and the total amount of DNA that can be

290 Decreased protofibril packing was confirmed in plasma for high thrombin concen

291 eezing, freeze-drying, air drying and vacuum packing, was evaluated on these potential aroma metaboli

292 , and PPP-NN, whose structures and molecular packing were examined by X-ray diffraction studies.

293 highlights the importance of considering the packing when analyzing dynamics of crystalline proteins.

294 ounced positive Gaussian curvature of layers packing, which are rare in the samples obtained by cooli

295 n in restricted nuclear space requires dense packing while ensuring DNA accessibility.

296 semiconducting polymer, and correlate chain packing with local electroluminescence by using external

297 sizes are arranged into a tetrahedral close packing, with exceptional translational order over lengt

298 luence three-dimensional cell morphology and packing within epithelial tissues.

299 ar strands and their hexagonal, antiparallel packing within the crystal.

300 hypothesized that disruption of the crystal packing would improve solubility, which led to a change