ライフサイエンスコーパス: protein composition

1 36 individual milk samples were analysed for protein composition.

2 nd its inhibition as a function of lipid and protein composition.

3 romoting changes in the extracellular matrix protein composition.

4 thern African oilseed legume with an unusual protein composition.

5 ting three crucial parameters that describes protein composition.

6 copy was performed on BCE-ECM to examine the protein composition.

7 , and is essential for controlling flagellar protein composition.

8 ction and HCMV-induced alteration of the MAM protein composition.

9 es of cells are asymmetric in both lipid and protein composition.

10 cells can adapt with substantial changes in protein composition.

11 arm set was the dominant influence factor on protein composition.

12 c flagella (PFs) have a unique structure and protein composition.

13 ive changes in myofiber cytoarchitecture and protein composition.

14 well as the resulting imbalances in cellular protein composition.

15 detergent, and characterized their lipid and protein composition.

16 an the wild type but showed no difference in protein composition.

17 ght, days to maturity, grain yield, and seed protein composition.

18 hate) formation and electron transport chain protein composition.

19 olipid-rich lipid domains with a specialized protein composition.

20 es that can tolerate considerable changes in protein composition.

21 e localized to cortical patches of differing protein composition.

22 , as is the glycerophospholipid and membrane protein composition.

23 ane compartments demonstrates a unique SNARE protein composition.

24 e rest of the membrane in specific lipid and protein composition.

25 issue directly involved in modifying urinary protein composition.

26 evidence that pre-mRNA splicing alters mRNP protein composition.

27 abnormal erythrocyte morphology and membrane protein composition.

28 g their morphology, thermal sensitivity, and protein composition.

29 that of excitatory axons in distribution and protein composition.

30 identity by defining positioning and surface-protein composition.

31 as an important principle in determining LD protein composition.

32 profound alterations in the lipid moiety and protein composition.

33 hesized that metformin intake influences the protein composition.

34 rowding plays a major role in determining LD protein composition.

35 for main-tenance of optimal plasma membrane protein composition.

36 duced the particle size without changing its protein composition.

37 ular organelle, the cilium contains a unique protein composition.

38 l domains, myelin ultrastructure, and myelin protein composition.

39 cific cuts of meat, based on their intrinsic protein composition.

40 otal nitrogen content to determine proximate protein composition.

41 ad NS milk, while the opposite was found for protein composition.

42 gating zone components in regulating ciliary protein composition.

43 ation, (e) oral mucosal pH, and (f) salivary protein composition.

44 ds of synapses to assess synapse density and protein composition.

45 of particles with atypical morphologies and protein compositions.

46 ference mapping of procapsids with different protein compositions.

47 nce is achieved relies on knowledge of their protein compositions.

48 eir amino acid compositions indicate altered protein compositions.

49 xample, differ strikingly in their lipid and protein compositions.

50 ith regard to their sizes, morphologies, and protein compositions.

51 ferent plasma membrane domains with distinct protein compositions.

52 racterized by differences in local lipid and protein compositions.

53 d by mammalian and avian hosts have distinct protein compositions.

54 nted into hundreds of domains with different protein compositions.

55 ic complexes with different morphologies and protein compositions.

56 ssue decellularization while maintaining ECM protein composition, 3D-architecture and physico-chemica

57 ted in the release of virions with irregular protein composition, abnormal particle density, and redu

58 to systematically define proapoptotic BCL-2 protein composition after stress and then directly inter

59 In agreement with the protein compositions, all three ISA complexes were missi

60 espite strong evolutionary conservation in r-protein composition among eukaryotes, Arabidopsis 80S ri

61 inct subpopulations of LDs differed in their protein composition and ability to recruit proteins.

62 lated native P-proteins to determine the SEO protein composition and analyzed the expression pattern,

63 es cerevisiae that RNA granules with similar protein composition and assembly mechanisms as mammalian

64 rize this purified activity, we analyzed its protein composition and assembly.

65 The protein composition and association of C/D snoRNPs with

66 rather reflect specific changes in synaptic protein composition and axonal structure.

67 ggest that KSHV virions indirectly alter the protein composition and chromatin modifications at ORF50

68 les at the base of the flagellum to regulate protein composition and cilium function.

69 icroscopy hybrid approach to determine the r-protein composition and conformation of 30S ribosome ass

70 ality and contain detailed information about protein composition and conformation, about post-transla

71 ple replicating core complexes with distinct protein composition and function in the centrosome of To

72 ational modification that can alter synaptic protein composition and function.

73 trix and the outer envelope, differ in their protein composition and functional properties.

74 In this report, the protein composition and fundamental progression of stres

75 in sufficient amounts and purity to analyze protein composition and histone modifications by mass sp

76 sperm centrioles are remodeled both in their protein composition and in ultrastructure, yet they are

77 rypanosome flagellar membrane, its lipid and protein composition and its proposed roles in sensing an

78 This HAC exhibits normal kinetochore protein composition and mitotic stability.

79 we performed a systematic survey of the FXR protein composition and mRNA association of FXGs in the

80 n specific circuits requires identifying the protein composition and mRNA cargos of the ribonucleopro

81 resembled authentic virus particles in their protein composition and neutralization sensitivity to an

82 oteins bind but instead actively defines the protein composition and organization of the RNP.

83 , how such gradients can be used to engineer protein composition and organization within a 3D tissue.

84 Whereas the protein composition and overall shape of several giant v

85 t the B. burgdorferi rpoS homolog influences protein composition and participates in stationary-phase

86 e that XMRV is indeed a gammaretrovirus with protein composition and particle ultrastructure highly s

87 x of the mutants were normal with respect to protein composition and processing, full-length genomic

88 derived from this treatment was examined for protein composition and reactivity in humoral and cellul

89 We analyzed protein composition and regulation of gene expression of

90 for synapse-specific control of active zone protein composition and release probability.

91 lexes are heterogeneous with respect to both protein composition and specific function.

92 In the present work, we evaluate the protein composition and stability over time and we syste

93 flagella known as archaella-distinct both in protein composition and structure from bacterial flagell

94 owed evaluation of correlation between flour protein composition and technological properties.

95 om-up proteomics approach to investigate the protein composition and the dynamics of protein expressi

96 The protein composition and the protein stoichiometry of the

97 etween viral and cellular membrane lipid and protein compositions and curvatures exist.

98 etween viral and cellular membrane lipid and protein compositions and curvatures exist.

99 like particles (VLPs) and affects VLP yield, protein composition, and morphology.

100 ainst oxidative modification, main lipid and protein composition, and size distribution).

101 haracterized to determine the structure, the protein composition, and the infectivity of the particle

102 adipocyte caveolae have a relatively limited protein composition, and they lack the raft protein, flo

103 lterations of nuclear envelope structure and protein composition are essential to many aspects of met

104 sis and lipid metabolism, their function and protein composition are poorly understood.

105 nules are generated; however, their size and protein composition are subtly altered.

106 processing, they appeared to have a similar protein composition as A19-containing virions.

107 .e., temperature, protein concentration, and protein composition, at which liquid-liquid phase separa

108 ly used for clinical diagnostics because its protein composition bears a wealth of information about

109 ing the Golgi may undergo further changes in protein composition before arriving at synaptic sites.

110 tosomes released from flagella have a unique protein composition, being enriched in a subset of flage

111 odel whereby Stn2 is required to preserve SV protein composition but is dispensable for maintaining t

112 ibrillar isolates demonstrated no changes in protein composition but showed increased prevalence of p

113 mains of neurons are known to have different protein compositions, but the molecular mechanisms that

114 anatomy of syd vesicles, we determined their protein composition by mass spectrometry.

115 Analysis of the protein composition by sodium dodecyl sulfate-polyacryla

116 by attenuating the changes in intracellular protein composition caused by aneuploidy.

117 echanisms, defined a linear pathway in which protein composition changes at endocytic sites control a

118 factors interact with that locus and how the protein composition changes in different cell types or d

119 We propose that the observed protein composition changes in the connecting filaments,

120 The protein composition collected in vitro mimics that colle

121 infectivity per particle, and has an altered protein composition compared with that of unmodified MV.

122 The protein composition (corona) of zeolite nanoparticles ha

123 ariant sequence of changes in cortical patch protein composition correlates with changes in patch mot

124 Granule protein composition depends on granule distance to the n

125 information (i.e., the information about the protein composition derived from the Raman spectra with

126 Because protein composition determines responses in individual c

127 ion of mice the Borrelia burgdorferi surface protein composition differs profoundly from that of tick

128 e spatial control of the remodelling of mRNP protein composition during directional transport and pro

129 ration and delineate specific changes in RNP protein composition during formation and transport of mR

130 r-cores) closely resembled native virions in protein composition (except for lacking cell attachment

131 formed in this system had the structure and protein composition expected of mature HSV-1 capsids, in

132 r groups that differ in average velocity and protein composition: fast component (FC), slow component

133 nisms regulate steady-state synaptic vesicle protein composition from shared early endosomes.

134 Although Mediator with different protein compositions has been isolated, it remains uncle

135 Plastid protein composition, however, seems to be largely unaffe

136 to the gating zone and may regulate ciliary protein composition; however, the mechanisms of ciliary

137 e resulting alterations in CRU structure and protein composition impairs E-C coupling and renders hea

138 s clarify the roles of the particle size and protein composition in HDL remodeling, and help reconcil

139 radation, providing bidirectional control of protein composition in local domains.

140 n-1 causes skin tethering by altering matrix protein composition in Tsk hypodermal connective tissues

141 psis thaliana) adjusts its physiology and Fe protein composition in vegetative photosynthetic tissue

142 y regulated remodeling of peroxisomal matrix protein composition in which the glyoxylate cycle enzyme

143 enal epithelial cells must maintain distinct protein compositions in their apical and basolateral mem

144 TACs demonstrated a considerable overlap in protein composition including RNA binding proteins.

145 were less stable and had an abnormal capsid protein composition, including a lack of capsid-stabiliz

146 ctrometry can be used to identify the intact protein composition, inclusive of post-translational mod

147 ions gave reasonably good representations of protein compositions indicated by sodium dodecyl sulfate

148 hod of RSV antigen delivery, rather than the protein composition, influences the phenotype of the ind

149 involving spatial and temporal variations of protein composition, interaction, and cellular tension.

150 Lateral inhomogeneity of lipid and protein composition is currently a subject of avid resea

151 ound an organelle called the pyrenoid, whose protein composition is largely unknown.

152 screte functional units, their complexity in protein composition is reduced relative to whole cells a

153 Its protein composition is tightly regulated through selecti

154 How the LD protein composition is tuned to the supply and demand fo

155 mes from a wide range of membrane lipids and protein compositions is demonstrated.

156 igin of amino acid occurrence frequencies in proteins (composition) is not yet fully understood.

157 changes in energy metabolism and sarcomeric protein composition, loss of cardiomyocytes, ventricular

158 This observation suggests that altered protein composition might affect the antiatherogenic and

159 aracterized biochemically by analysis of VLP protein composition, morphologically by electron microsc

160 brane properties such as phospholipid and/or protein composition, morphology, and microscopic charact

161 ardiac catheterization, perturbations in the protein composition occurred but returned to baseline va

162 The rebalancing of protein composition occurs with small alterations to the

163 e first to provide a more global view of the protein composition of a photosynthetic membrane from an

164 n identification technology) to identify the protein composition of basal bodies (centrioles) isolate

165 Here we examined the protein composition of canine parvovirus capsids and eva

166 ion of the low molecular mass (< or =45 kDa) protein composition of canine rectus muscle homogenates,

167 ce relationships indicate that, although the protein composition of Chlorobium-type chlorosomes is su

168 "knocksideways" system and then compared the protein composition of clathrin-coated vesicle (CCV) fra

169 involves no quantitative change in the known protein composition of desmosomes.

170 These experiments establish that the protein composition of different F-actin structures is d

171 Ankyrin-G (AnkG) coordinates protein composition of diverse membrane domains, includi

172 in an mTOR-dependent manner, we analyzed the protein composition of DRGs from mice in which we geneti

173 in a Rab5-dependent manner, VipD alters the protein composition of endosomes thereby blocking fusion

174 rate of QDs was positively correlated to the protein composition of EPS (defined by the ratio of prot

175 The distinct protein composition of ETEC vesicles and their ability t

176 Here, the protein composition of exosomes from Mtb-infected and un

177 Changes in the host protein composition of exosomes from Mycobacterium tuber

178 ng and Western blot analyses showed that the protein composition of exosomes released in the presence

179 with Mtb leads to significant changes in the protein composition of exosomes.

180 Protein composition of fresh muscle and of meat aged was

181 We have analyzed the protein composition of Golgi-derived coat protomer I (CO

182 Characterization of the protein composition of hAH will identify molecules invol

183 t comprehensive view to our knowledge of the protein composition of HCV and new insights into the com

184 nds to environmental changes by altering the protein composition of its outer membrane.

185 The lipid and protein composition of LDs is highly dynamic and influen

186 the neuronal membrane and alterations in the protein composition of lipid rafts.

187 to the analysis of membrane proteins and the protein composition of membrane preparations.

188 Using this approach, they assayed the protein composition of mitotic chromosomes, identifying

189 Analyses of the protein composition of oligo(dT)-selected UV photocross-

190 l ATGL partner and provide evidence that the protein composition of perilipins at the LD surface regu

191 m-specific roles for apoE in determining the protein composition of peripheral nerve as well as regul

192 Little is known about the protein composition of plant telomeres.

193 tudy represents a definitive analysis of the protein composition of prostatic CA and calculi and sugg

194 Analysis of the protein composition of purified extracellular virions in

195 hormone-binding function by changing the TPR protein composition of receptor complexes and that TPR p

196 increased defective particle formation, the protein composition of secreted virions was largely unch

197 size was associated with divergence in major protein composition of seminal vesicle fluid, suggesting

198 cking pathways that shape the morphology and protein composition of sensory cilia in C. elegans.

199 in neurotransmission because it dictates the protein composition of synaptic vesicles, the organelle

200 ic vesicle proteins and an alteration of the protein composition of synaptic vesicles.

201 ssing factors have been identified, the full protein composition of the 3' processing machinery has n

202 ofile analysis, we predict the existence and protein composition of the archaeal counterpart of the e

203 uantitative mass spectrometry, we define the protein composition of the assembly intermediate and une

204 The purpose of this study is to compare the protein composition of the B-3 line of transformed human

205 A) resulted in changes in the outer membrane protein composition of the bacterium.

206 o changes in the overall architecture or the protein composition of the brain or alterations in perip

207 luding quantitative mass spectrometry of the protein composition of the capsids, revealed that both p

208 The structure and protein composition of the cardiac CRU is significantly

209 al of the accessible exon regions alters the protein composition of the complex, but the core spliceo

210 l region of RNase E, thus affecting both the protein composition of the degradosome and the endonucle

211 laminae in the developing nervous system the protein composition of the embryonic retinal basal lamin

212 g introns, pre-mRNA splicing greatly impacts protein composition of the emerging mRNP.

213 nectin-1-null mice were hypomineralized, the protein composition of the enamel matrix was unaltered.

214 onal polyacrylamide gels further defined the protein composition of the extracted chromosome fraction

215 The sequential changes in protein composition of the fibrils in the developing mus

216 To begin an analysis of the protein composition of the flagellar tip, we used differ

217 This review summarizes the main changes in protein composition of the glomerular mesangium and base

218 Understanding the protein composition of the inner nuclear membrane (INM)

219 Although the protein composition of the IRVs is well studied, the mec

220 ene expression program, we have examined the protein composition of the KSHV particle.

221 Analysis of the protein composition of the large-subunit intermediates i

222 Analysis of the protein composition of the MFGM of wild type and BTN1A1

223 Despite the apparently normal protein composition of the mutant erythrocyte membrane,

224 In contrast with vertebrates, the protein composition of the NE and the function of NE pro

225 Establishing the distinct protein composition of the periarbuscular membrane is cr

226 h spatial and temporal information about the protein composition of the periarbuscular membrane.

227 s multiple cellular processes, including the protein composition of the plasma membrane, intercellula

228 Endocytic mechanisms control the lipid and protein composition of the plasma membrane, thereby regu

229 Dynamic changes in membrane protein composition of the primary cilium are central to

230 The membrane protein composition of the primary cilium, a key sensory

231 Examination of the protein composition of the purified Snf1 enzyme complexe

232 The endotoxin, phospholipid, and protein composition of the recovered blebs indicate that

233 e then employed to characterize the specific protein composition of the resulting complexes.

234 Neither the exact protein composition of the T6SS organelle nor the mechan

235 Although the protein composition of the terminals of ribbon synapses

236 Importantly, the cytoskeletal protein composition of the TM cells was also found to be

237 These cells are highly polarized, and the protein composition of their apical and basolateral memb

238 ese cell types, are a result of the membrane protein composition of these cells.

239 To understand the protein composition of these unique postmitotic cells, i

240 cholesterol ester, and triglyceride, but the protein composition of this compartment is largely unkno

241 TP synthases from all forms of life, yet the protein composition of this domain changed during evolut

242 a mass spectrometry strategy to identify the protein composition of this nuclear organelle purified f

243 tion and progression of caries; however, the protein composition of tooth enamel has not been fully c

244 ognate sub-sites at L and R, analysis of the protein composition of transpososomes thus obtained, and

245 for the VE proteins and determination of the protein composition of two forms of HMWPs.

246 While the protein composition of various yeast 60S ribosomal subun

247 emonstrated that macrophage responses to the protein composition of vesicles required the adjuvantlik

248 ween the two membrane domains, the lipid and protein compositions of flagella and cilia are distinct

249 A lack of methods for measuring the protein compositions of individual synapses in situ has

250 However, the protein compositions of Piwi complexes, the critical pro

251 The distinct and overlapping protein compositions of reported MRB1 complexes and dive

252 a demonstrate early changes in the lipid and protein compositions of specific HDL subspecies in adole

253 The quantitative protein compositions of the Osborne fractions determined

254 In contrast, the protein compositions of the outer permeability barriers

255 Analyses of the protein compositions of these complexes confirmed previo

256 e conditions and identified both the RNA and protein compositions of these RNP complexes.

257 Protein compositions of wild-type and ICP0 null virions

258 the impact of indoor vs outdoor-reared meat protein composition on digestion and to associate protei

259 could not be attributed to changes in virion protein composition or production of defective interferi

260 The protein compositions, or the proteomes, found in human s

261 ve ISVPs (infectious subvirion particles) in protein composition, particle morphology, and capacity t

262 little was known about their outer membrane protein composition prior to the recent sequencing of th

263 Shank1 mutants showed altered PSD protein composition; reduced size of dendritic spines; s

264 in the amount, ratio, or integrity of their protein composition relative to an isogenic wild-type vi

265 ses, including defects in virion morphology, protein composition, reverse transcription, nuclear impo

266 herapy partially reverses the changes in the protein composition seen in HDL(3) in coronary artery di

267 Analysis of their protein composition showed that they are composed nearly

268 on coefficient, the buoyant density, and the protein composition similar to the insulin-responsive Gl

269 residues that resulted in changes in gluten protein composition, specifically the percentage of the

270 n adult mice led to improvements in synaptic protein composition, spine density and neural function i

271 an apparent mass in excess of 1.4 MDa, whose protein composition substantially changes in response to

272 e with niacin/statin treatment resulted in a protein composition that more closely resembled that of

273 e inner ear have a specialized structure and protein composition that underlies their sensitivity to

274 Despite knowledge of its protein composition, the molecular architecture of the r

275 this system focusing on the following: its 8-protein composition, their individual and synergistic ac

276 Remarkably, despite retaining similar protein composition, there are exceptional architectural

277 an essential role in regulating cell surface protein composition, thereby impacting numerous cellular

278 dosomal membranes and alters their lipid and protein composition, thereby protecting the pathogen fro

279 Based on their RNA and protein compositions, these complexes are likely to repr

280 g signaling, cells regulate ciliary membrane protein composition through cytoplasmic action of the re

281 To restrict changes in protein composition to activated synapses, proteins may

282 flagellar ectosomes, we have compared their protein composition to that of the flagellar membrane fr

283 Native SMN complexes of identical protein composition to those isolated by immunoprecipita

284 tidylcholine/sphingomyelin ratio and (2) the protein composition visualized on a two-dimensional gel.

285 our different protein chip surfaces, and the protein composition was analyzed using a surface-enhance

286 mal subunits were isolated and their RNA and protein composition was characterized.

287 cterial expression plasmid (pET-32), and the protein composition was confirmed by both DNA sequencing

288 changes in certain metabolic parameters and protein composition were also observed.

289 The differences in protein composition were correlated with previously desc

290 Alterations in protein composition were detected by spectral counting a

291 DL-induced dynamic alterations in lipid raft protein composition were found to facilitate this moveme

292 ( approximately 5%), but differing in their protein composition were obtained from an aqueous maize

293 ctions of EMVs are highly dependent on their protein composition, which can dictate pathogenicity.

294 e effects of UVR on protein conformation and protein composition, which were confirmed by sodium dode

295 e that influenza virions share an underlying protein composition with exosomes, suggesting that influ

296 LB mutant) in membranes of defined lipid and protein composition, with full retention of Ca-dependent

297 We also determined ion channel protein composition within the endothelium of intramuscu

298 We suggest that protein composition works alongside the genetic code to

299 ds on dynamic regulation of ciliary membrane protein composition, yet we know little about the motors

300 Subcellular compartments have unique protein compositions, yet protein synthesis only occurs