ライフサイエンスコーパス: packing

1 tifs that are known to be important in helix packing.

2 ar structures, which prevent space-efficient packing.

3 unprecedented C(2) symmetry and an efficient packing.

4 stabilized through interdigitated glutamine packing.

5 fluorophores can significantly perturb lipid packing.

6 it did cause saturable alterations in lipid packing.

7 -ordered phase with a potential orthorhombic packing.

8 tructures reveal intricate three-dimensional packing.

9 higher-order oligomers through side-by-side packing.

10 MOF-74, CPM-74 is made from homohelical rod packing.

11 t drives the tissue toward optimal geometric packing.

12 nfigurations of PCG segments in a melt state packing.

13 le to changes in chromatin transcription and packing.

14 of Brownian molecular dynamics and geometric packing.

15 conserved motif that facilitates hydrophobic packing.

16 de-by-side and tail-to-tail nearest-neighbor packing.

17 aggregations of topological defects in cell packing.

18 ptor (D-A) chromophores, and their molecular packing.

19 eton and acts as a mechanical sensor of cell packing.

20 ane lipids, inducing a reduction in membrane packing.

21 e shape and mildly shrink above random close packing.

22 l and geometric information of dry colloidal packings.

23 one-bond-flip occurs, whereas, in a tighter packing (7% smaller unit cell size), the hula-twist occu

24 n, H2Bub activates the enzymatic assembly by packing against Swd1 and alleviating the inhibitory effe

25 he native folds of membrane proteins, but is packing alone sufficient to drive folding in lipids?

26 he most compact and close to the ideal cubic packing among the Al-B-C phases containing B(12)-type ic

27 ignificantly shorter, and exhibit disordered packing and a 30% decrease in packing density.

28 r evidence of crowding as nuclei reach close-packing and are quantitatively described by a nonlinear

29 s of polymers with ten sub-units since close packing and co-alignment of neighbouring groups cannot b

30 These results show that alternative core packing and consequent allosteric modulation of binding

31 cess of few to many mono layers, the crystal packing and deep level defects.

32 A higher applied pressure leads to a compact packing and densification of films resulting in an impro

33 supported by the coordination of the atomic packing and electronic factors.

34 se the importance of sufficient initial coil packing and frequent control of neck region of the aneur

35 The packing and geometries of residues are characterized her

36 for the role of N in SARS-CoV-2 viral genome packing and in host-protein co-opting necessary for vira

37 l giant unilamellar vesicles (GUVs) on lipid packing and lateral segregation of cholesterol in the bi

38 f different functional pressures on the core packing and ligand recognition of the SH3 domain from hu

39 . smegmatis (Msm) underscored by their lipid packing and lipid dynamics.

40 which act as a binder to improve interlayer packing and load transfer in the multilayer films.

41 amics to mixing-induced changes in the lipid packing and membrane structure.

42 olesterol, resulting in recovery of membrane packing and permeability.

43 ed sour gas feeds, controlling polymer chain packing and plasticization tendency of such polyimide me

44 vide improved access to lymph nodes, optimal packing and presentation of antigens, and induction of a

45 ncy in the lens is accomplished by the dense packing and short-range order interactions of the crysta

46 Cyclized GDGTs increase membrane packing and stability, which has been shown to help cell

47 sembling peptides influences molecular-level packing and supramolecular morphology.

48 In some instances, during industrial-volume packing and transportation, coated seeds do not flow wel

49 ced by the coupling between enhanced protein packing and weakly unfavorable lipid desolvation, or sol

50 in generating the unusual structure through packing and/or dispersion forces is discussed.

51 As a result, we are able to tune the crystal packings and optical gaps of the solids and see the mome

52 The synergy among pore volume, guest packing, and linker conformation that characterizes this

53 rences in properties, processing conditions, packing, and material state(s).

54 Random packings are crucial in understanding arrangement and ge

55 echanisms, the molecular architecture and/or packing arrangement of the chromophores are vital for th

56 s highly sensitive to the specific molecular packing arrangement within a noncentrosymmetric lattice,

57 V and I/II pairs exemplify the T-shaped heme packing arrangement, prevalent in multiheme cytochromes,

58 . Structural analysis reveals that different packing arrangements and orientational disorder of the s

59 eoretical calculations, revealing that their packing arrangements are governed by distinct pai-pai-st

60 ar materials depend on the molecules' mutual packing arrangements.

61 ures, when cholesterols likely to be crystal packing artifacts are excluded.

62 y) and its influence on the bonding, crystal packing as well as the excited state energies and lifeti

63 oward the superhelical axis produces tighter packing, as determined by the size of the coiled-coil ra

64 ents in the gA subunits and changes in lipid packing, as well as water reorganization, that occur dur

65 We find that dry colloidal packings, as characterized by contact number and packing

66 ion on solute transport through a glass bead packing at different saturations.

67 Other mutations increase hydrophobic packing at the gp120 inner-outer domain interface and we

68 des a fundamental understanding of soft JNPs packing at the water-oil interface and provides a strate

69 Concomitantly, membrane morphology and lipid packing became disrupted.

70 e E217G hairpin exhibits an altered adaptive packing behavior stemming from an additional GXXXG helix

71 naccessible data revealed a range of notable packing behaviors, including four different space groups

72 ble molecules can exhibit a rich and complex packing behaviour.

73 membrane recruitment of Rab5 and acyl chain packing being critical for domain formation.

74 ructures offer a platform for intermolecular packing beneficial for the formation of liquid crystalli

75 exposure, the lamellar order present in new packing boxes is disrupted by the weathering process.

76 ed strategies aimed at altering PHD2 crystal packing by protein modification and molecules that bind

77 or packing (group 1, n = 25), 1-week ostium packing by ribbon gauze (group 2, n = 29) or non-medicat

78 Disruption of steric packing can destabilize the native folds of membrane pro

79 Since molecular packing can determine the functional properties of mater

80 gnetic relaxation behavior is due to crystal packing changes rather than changes to the crystal field

81 6, IT-4F, and IEICO-4Cl, and their molecular packing characteristics and miscibility are studied.

82 and redesign of variants, we define a steric packing code underlying its assembly.

83 Rate-based calculations in packing column demonstrated a kinetic control with highl

84 may offer direct evidence for adhesive loose packings comprising dry small particles, as proven by X-

85 ouches with different O(2) permeability) and packing conditions (cover brine, air or N(2) atmosphere)

86 The experimentally measured packing configuration and inferred interparticle forces

87 fan-shaped molecules tend to form hexagonal packing cylindrical phases, the cone-shaped molecules co

88 Despite the importance, packing defects (i.e., cavities including voids, pockets

89 are disordered and increase the amount of PL packing defects and the PL tail order.

90 ng a significant amount of chemically unique packing defects, and the acyl chains extended toward the

91 uce the notion of a "crystallographic sphere packing," defined to be one whose limit set is that of a

92 onic strength) can be employed to adjust the packing degree and the spatial position of microfibrilla

93 ral lipids but presenting equal phospholipid packing densities differentially recruit AHs.

94 rils with narrow cross sections can optimize packing densities in the fibrillar core structure, in co

95 of amyloid fibrils is, indeed, driven by the packing densities of residues and H-bonds.

96 work topologies, degree of interpenetration, packing densities, and the specific spatial arrangement

97 400 m(2) g(-1)), hierarchical porosity, high packing density (1.41 g cm(-3)) and high nitrogen (N) co

98 ts suggest that clutch size may regulate DNA packing density and gene activity.

99 chromatin irregular, they may not alter the packing density and size of the fiber.

100 e, and use this to quantify variation in the packing density and to characterize the different liquid

101 tetrafluoroethylene) (PTFE), with a particle packing density at the theoretical maximum.

102 rhodopsin molecules and decreased rhodopsin packing density compared to wild-type discs.

103 we show that Mga2 senses the molecular lipid-packing density in a defined region of the membrane.

104 T, which in turn reflects the macromolecular packing density inside droplets.

105 Maximizing packing density is therefore a critical technical challe

106 th 100% loading and trapping efficiency at a packing density of 110,000 droplets per in(2).

107 2-D NM frameworks with a packing density of 75%, representative of most 2-D NM me

108 A high packing density of 90%, which to our knowledge has yet t

109 the polymer chains can deform influences the packing density of the JNPs at the interface.

110 in microtubule number, and increases in the packing density of these polymers, which collectively br

111 nized into layers distinguished by the size, packing density, and connectivity of their constituent n

112 ings, as characterized by contact number and packing density, are quite consistent with adhesive loos

113 tin electrostatic interactions influence the packing density, clustering of nucleosomes, and the widt

114 This reveals that a regular side-chain packing density, independent of conformational isomers,

115 rs via inkjet printing with 110 pixels/mm(2) packing density.

116 a JNPs assembly with a lower initial lateral packing density.

117 atures, such as their morphology or cellular packing density.

118 bit disordered packing and a 30% decrease in packing density.

119 rated membranes, by increasing the bilayer's packing density.

120 is, separations conducted with much smaller packing diameters, results in retention factors that are

121 ion induced structural transformation due to packing disorder in bilayer has been delineated through

122 rther improved when we also account for cell packing disorder.

123 highly ordered hexagonal phase or frustrated packing driven by directional interactions which for som

124 In terms of nucleic acid packing, dsDNA viruses, which lack genome segmentation a

125 remain unchanged upon heating), we find that packing effects can override this preference and give ri

126 cted by X-ray crystallography due to crystal packing effects.

127 n of the sn1 tail length, limiting gas-phase packing efficiency.

128 e physicochemical properties, single-crystal packing, end-group redistribution propensity, and BHJ ph

129 the poly-[n]-catenane by the analysis of the packing energy in terms of monomeric and dimeric cages.

130 We also performed the packing experiment of filaments and membranes to demonst

131 (d) 3.5 mum at mildly acidic pH) and crystal packing favoring the 4 + 4 complex.

132 metal electrode and a standard photovoltaic packing film.

133 egarding how the two competing requirements, packing for stability vs. cavities for function, are rec

134 resulted in the most favorable "brick-layer" packing for triisobutylsilyl-DNBDC and a charge mobility

135 that significantly deviate from random loose packings for hard spheres.

136 However, it was unclear if crystal packing forces played a role in stabilizing the two-fold

137 We show that, when the apparent friction and packing fraction are normalized by their cohesion-depend

138 cal properties such as apparent friction and packing fraction are still elusive when inertial, cohesi

139 with different architectures at a variety of packing fractions and solvent conditions.

140 ration results in increase of droplet sizes, packing fractions and viscosity, while decrease in value

141 r because these viruses have typically lower packing fractions than viruses encapsidating naked dsDNA

142 At even higher packing fractions, microgels solely shrink.

143 ctions of the ion with nearby waters, 2) the packing free energy that is the work to produce a cavity

144 ED without topical mitomycin: no stenting or packing (group 1, n = 25), 1-week ostium packing by ribb

145 e energy levels and optimizing the molecular packing, high-performance optically switchable organic t

146 The resulting threads assume crystalline packing hundreds of micrometers across.

147 We describe a theory of packing hyperboloid "diabolic" domains in bend-free text

148 ofiles along the bilayer normal, and lateral packing (i.e., average surface area per lipid).

149 ion, which are strongly coupled to the guest packing in and the shape of the peripheral pockets, to a

150 photoreceptors, in vivo data describing cone packing in children is limited.

151 tain high photoluminescence and highly close packing in solid state thin films, and the fabricated re

152 little information about the local molecular packing in supercooled liquids, meaning that the order p

153 o replace Cys or Leu, respectively, disrupts packing in the hydrophobic core and lowers RD3's apparen

154 le the alkyl pending groups affect molecular packing in thin films and affect the long-term performan

155 ess and to characterize the emergent nuclear packing in this system.

156 uration of the lipid acyl chain (i.e., lipid packing) in the synthetic lipid vesicles.

157 Packing interaction is a critical driving force in the f

158 ture and revealed the importance of nonpolar packing interactions of the fifth sugar.

159 ur data suggest that cross-strand side chain packing interactions within the same beta-sheet may play

160 , despite sequence similarity at the lateral packing interface, HEAT_R1 and LRV_M3Delta1 filaments ad

161 rical roles within the structures, and their packing into a novel superstructure with unexpected thre

162 different morphologies, the crystallographic packing is nearly identical and is not affected by the t

163 This difference in packing is spectacularly amplified at the whole surface

164 contribute, but the nature of transmembrane packing is unclear.

165 Importantly, such molecular packing leads to (i) the formation of delocalized and em

166 The phospholipid packing level regulates mainly the amount of neutral lip

167 condense DNA in sperm to almost crystalline packing levels.

168 et protein, which may contribute to the high packing limit of this unique protein.

169 at extremely high concentrations nearing the packing limit, corresponding to only a few water layers

170 D simulations, we suggest that the headgroup packing limits the ligand density, rather than the sulfu

171 er size, chain conformational order, lateral packing, lipid phase, and morphology) and the protection

172 f Archaea to adjust membrane composition and packing may be an important strategy that enables surviv

173 ology couples a realistic description of the packing media (polyurethane foam without a biofilm) obta

174 Such a new molecular packing mode, in combination with the demonstrated semic

175 ructed in solution state and their molecular packing models are rationally understood.

176 cal calculations allowed us to elucidate the packing modes of both supramolecular polymorphs A and B,

177 The dimeric macrocycle adopts a columnar packing motif in the solid state with large void spaces

178 impact of introducing a common natural helix packing motif to the transmembrane domain of a genetical

179 antiomers in its solid state with intriguing packing motif.

180 sts in the framework, resulting in different packing motifs depending on the position, type, and numb

181 ructural connections between the short-range packing motifs in the amorphous precursor and those obse

182 to increase luminescence, or modifying chain packing motifs to improve percolation charge transport;

183 exhibited twisted bridges and near-cofacial packing motifs with oppositely or parallel pai-stacked s

184 However, despite having very similar crystal packing motifs, the three compounds exhibit distinct pho

185 MicroED) for rapid assessment of solid-state packing motifs, using a class of chiral nanocarbons-expa

186 roduce the pair statistics of the disordered packings observed in embryos and recover the scaling rel

187 id films, the slipped stacked intermolecular packing of a thiophene-functionalized derivative leads t

188 plaque load, suggesting that the microglial packing of Abeta into dense plaque is an important neuro

189 To see whether slow packing of alpha-helices 1 and 3 is reflected in the rat

190 relation map that defines the supramolecular packing of alpha-synuclein within the fibrils.

191 sing from the self-reconfiguration and close packing of an initial assembly of identical "deformable"

192 The regular packing of atoms, molecules and nanoparticles provides t

193 ute a fundamental geometry for the efficient packing of connected layers or sheets.

194 The dense crystal packing of CQDs in the layered fashion suppresses local

195 of models (stereochemistry, hydrogen bonds, packing of domains and chain fragments, missing residues

196 demonstrate that the canonical model for the packing of dsDNA can be extended to dsRNA viruses.

197 However, the dense packing of dyes can result in not only compromised DNA a

198 menagerie of bend-free textures akin to the packing of focal conic domains in smectic liquid crystal

199 ne and small amino acid residues allow close-packing of helices on the matrix side.

200 ptic network due to the small size and dense packing of its elements.

201 deed, nanoscale imaging revealed coordinated packing of L-type Ca(2+) channels and RyRs into dyadic j

202 s is revealed, which explains why the denser packing of larger apolar domains of the guests does not

203 Chiral packing of ligands on the surface of nanoparticles (NPs)

204 ther systems combining nitrogen with the TCP packing of metals will be similarly driven toward interg

205 res a fundamental understanding of how close packing of molecules can affect structure and function.

206 improvements made in the production and the packing of monodisperse spherical particles for nanoflow

207 of the end-group substituent on the crystal packing of nonfullerene acceptors.

208 The structure and packing of organic mixed ionic-electronic conductors hav

209 due to the inherent inability to control the packing of organic molecules in the solid state.

210 Less dense packing of particles at the root surface was hypothesise

211 and wide-angle X-ray scattering examines the packing of PE chains into semicrystalline lamellae.

212 ells in the colony physically constrains the packing of proliferating cells and, thus, controls colon

213 During the seed-mediated growth, the atomic packing of Ru overlayers follows an fcc lattice, in cont

214 nd P-body proteins, which suggests regulated packing of seed mRNAs.

215 The tight packing of selected compounds within the enzyme contribu

216 as well as providing wider insights into the packing of self-assembled structures.

217 Using efficient algorithms for the packing of shapes, we enumerate millions of low-energy c

218 electronic properties as well as the crystal packing of the buckybowls.

219 A proper chiral packing of the building block at several molecular scale

220 s yielded a highly unusual three-dimensional packing of the conjugated backbone, which is likely resp

221 sembly that was generated by the hydrophobic packing of the conserved amphipathic helices alpha1 and

222 Mutations that destabilize the packing of the domain's hydrophobic core have little eff

223 e sensitive, representing differences in the packing of the hexapeptides within the globules.

224 The exact packing of the hydrazone rods within the cylinders and l

225 Instead, it is likely that the dense packing of the oxidative phosphorylation complexes in th

226 idized nDsbD, local frustration disrupts the packing of the protective cap-loop region against the ac

227 s driven by hydrogen bonding and hydrophobic packing of the residues from the central and C-terminal

228 al ATPase activity and upon heptamerization, packing of trans-acting Tyr(290) against cis-acting Arg(

229 hain motion that compromises the hydrophobic packing of two core helices.

230 ack between WNT11 and GDNF permits the dense packing of ureteric tips.

231 tivation of the nucleation site favoured the packing of vesicles and the formation of the froth struc

232 overning the molecular geometries and unique packing of Y6 and CH1007 to ensure their superior charge

233 find that the distinctive pai-pai molecular packing of Y6 not only exists in molecular single crysta

234 We explore experimentally random packings of dry colloids with X-ray nanotomography that

235 Random packings of dry small particles may be subject to adhesi

236 rical and topological features of disordered packings of rubber bands in a cylindrical container.

237 y; even when a protein crystallises, crystal packing often influences ligand-binding and protein-prot

238 s the ligand density, rather than the sulfur packing on the nanoparticle surface, for ~10 nm and larg

239 Patients receiving any packing or stenting achieved better anatomical (96% vers

240 pped AuNSs confirm greater hydrophobic chain packing order and saturation of charged headgroups withi

241 ffusion slowdown is not due to altered lipid packing order but may instead be attributed to local pro

242 ere not able to detect a change in the lipid-packing order during the initial stage of protein bindin

243 ing of membrane topography, diffusivity, and packing order in live mammalian cells through a synergy

244 otein changes, we have deduced how the lipid-packing order is altered in different stages of the pore

245 A significant change in the lipid-packing order takes place during assembly of pre-pore ol

246 brane diffusivity drops with increased lipid packing order when comparing the endoplasmic reticulum (

247 The induced domains have distinct lipid packing/order compared to the symmetric liquid-disordere

248 Both hydrophobicity and the "geometric packing parameter" dictate small molecule compatibility

249 s an alpha-helical secondary structure and a packing pattern that is reminiscent of the cross-alpha a

250 Our new insights into 3D droplet packing permit the fabrication of complex synthetic tiss

251 A series of unconventional spherical packing phases in PBIs, including A15 phase, sigma phase

252 as long-term care facilities, prisons, meat-packing plants, produce processing facilities, fish fact

253 Solid-state packing plays a defining role in the properties of a mol

254 pects bears close resemblance to concomitant packing polymorphism in crystals, should help bridge the

255 promote selectivity, while larger inter-UBU packing pores increase uptake capacity.

256 ty is mainly from UBU ultramicropores, while packing pores promote C(2) H(2) uptake capacity.

257 ults in stiffer bilayers with distinct lipid packing properties.

258 Thus, accurate protein side-chain packing (PSCP) is a critical step toward protein structu

259 s ensemble of fiber structures with variable packing ratios, sedimentation coefficients, and persiste

260 Because cellular packing requires that cone elongation accompanies foveal

261 out atomically resolved D:A interactions and packing reveals that the high performance of over 15% ef

262 th copper(II) provided assessment of lattice packing, ring contortion, and evidence of conformational

263 gh the curvature-targeting amphipathic lipid packing sensor (ALPS) motif of ATG14.

264 s a structurally conserved amphipathic lipid packing sensor motif, confirmed by liposome interaction

265 nce-restraints (DR) and the Symmetry-Imposed Packing (SIP) filters.

266 evaporative concentration leads to enhanced packing, stabilization (jamming) and point sintering wit

267 matrix strategy to engineer the surface and packing states of Pe-QD solids is demonstrated by a mild

268 res are guided by the complementary internal packing strains of Mn-Si and Mn-N domains, an effect kno

269 rotein crowding in the OXPHOS system imposes packing stress on the lipid bilayer, which is relieved b

270 trolling wave velocity and dispersion, while packing structure alone quantitatively explained most of

271 Results revealed that both packing structure and interparticle force heterogeneity

272 Unraveling the packing structure of dense assemblies of semiflexible ri

273 the embryo can robustly preserve the nuclear-packing structure while being densified.

274 of the formation of unconventional spherical packing structures in soft matter.

275 where conformational sampling and frustrated packing takes place over longer time scales.

276 idermis, but to changes in cell geometry and packing that arise from the open neural tube characteris

277 importantly, these assemblies show nonclose packings that afford voids to accommodate solvent molecu

278 ty, are quite consistent with adhesive loose packings that significantly deviate from random loose pa

279 onally, FASPR achieved the highest speed for packing the 379 test protein structures in only 34.3 s,

280 mers within the crystal lattice: in a looser packing, the one-bond-flip occurs, whereas, in a tighter

281 past, we challenge this paradigm for ordered packings, the fabrication of which are now feasible thro

282 developed organic CO prodrugs that allow for packing this gaseous molecule into a dosage form for the

283 fate specification in mostly motionless cell packings, this finding emphasizes the role of cell motio

284 cription of self-similar dynamics of nuclear packings, this model generates dynamic meshes for the co

285 structures that show different inter-domain packing through a short linker and refolding of CD2.

286 Nearly perfect co-facial packing to marginally or extensively shifted co-facial s

287 reciprocating "large-large-small" amino acid packing to mediate the interaction of the beta3 and alph

288 t Eag chaperones mimic transmembrane helical packing to stabilize effector TMDs.

289 Clearly, packing too much or too little fuel would lead to subopt

290 id molecular material, where a corresponding packing type can be selected or even promoted.

291 ray diffraction (XRD) analysis confirmed the packing variation in the columnar lattices regulated by

292 s the hydrophobic nature of the phospholipid packing voids that controls the binding level of AHs.

293 1-week ostium packing was found to be as effective as 8-week bicanalic

294 With this improved control over droplet packing, we can 3D-print functional synthetic tissues wi

295 w-density phase involves increased molecular packing, whereas that of the high pressure phase involve

296 sts the transmembrane domain explores looser packing which would facilitate activation.

297 to avoid local free volume due to irregular packing, which can host trapping impurities.

298 of conformally inequivalent crystallographic packings with all radii being reciprocals of integers.

299 omorphism and the control of epithelial cell packing, with potential implications for understanding t

300 to form heterochiral rather than homochiral packings, with heterochiral pairs being more likely to p