ライフサイエンスコーパス: phospholipid

1 glycerol, PG, another low-abundance class of phospholipids).

2 nd was critical for AA release from membrane phospholipids.

3 ng and anti-inflammatory effects of oxidized phospholipids.

4 E5 to limit polar interactions with membrane phospholipids.

5 otein trafficking, and the cellular roles of phospholipids.

6 membrane microdomains enriched with specific phospholipids.

7 esters, surrounded by a single monolayer of phospholipids.

8 little is known about its activity on diacyl phospholipids.

9 dinating the polar head-groups of transiting phospholipids.

10 e used for the de novo synthesis of membrane phospholipids.

11 major oxidation products of the unsaturated phospholipid 1-palmitoyl-2-arachidonoyl-sn-glycero-phosp

12 lesterol were prepared using three different phospholipids (1,2-dimyristoyl-sn-glycero-3-phosphocholi

13 The truncated tail phospholipids, 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-

14 L3 larvae with PLA2g1B, which reduced larval phospholipid abundance.

15 ne lipid transporter proteins that transport phospholipids across cellular membranes.

16 ophysical methods, here we show that anionic phospholipids activate the cpSRP receptor cpFtsY to prom

17 Cardiac mitochondrial phospholipid acyl chains regulate respiratory enzymatic

18 changes in the acyl chain composition of ER phospholipids affect SREBP-1c maturation in physiology a

19 d membranes, a pronounced disordering of the phospholipid alignment is observed.

20 reveal an unforeseen metabolic function for phospholipid and histone methylation intrinsic to the li

21 id synthesis, membrane protein biosynthesis, phospholipid and membrane protein trafficking, and the c

22 ent with previously reported data on altered phospholipid and receptor binding, we hypothesize that m

23 of hydrogen bonds between the polar zone of phospholipid and the OH groups of phenolic compounds.

24 c interactions between negatively charged PM phospholipids and basic amino acids found in K-Ras4B (K-

25 ospholipon 90H) or unsaturated (Lipoid S100) phospholipids and characterized for size, polydispersity

26 Additionally, phospholipids and cholesterol preferentially accumulated

27 ally driven by dextran depletants instead of phospholipids and cholesterol with prominent electrostat

28 ate from the interdigitation between surface phospholipids and core neutral lipids that occurs in LDs

29 ifungal activity, recruits multiple membrane phospholipids and forms oligomers in their presence.

30 iacylglycerol accompanied by the increase of phospholipids and free fatty acids.

31 OCFAs were determined in plasma phospholipids and hepatoma cells by gas chromatography.C

32 udied the enzymatic modification of egg yolk phospholipids and its effect on physicochemical properti

33 ted bacterial effectors can bind to membrane phospholipids and may regulate membrane trafficking.

34 so addresses other factors, including acidic phospholipids and modification of ENaC cytoplasmic cyste

35 d droplets (LDs) are covered with a layer of phospholipids and oleosin and were extensively studied b

36 The good found content of phospholipids and omega3-polyunsaturated fatty acids enc

37 B1 from Shigella flexneri may bind to acidic phospholipids and regulate actin filament dynamics.Micro

38 Hindered diffusion of phospholipids and sphingolipids is abolished in the GPMV

39 The roles of phospholipids and the C-terminal domain in subcellular l

40 chain-dependent differential localization of phospholipids and triacylglycerols was observed within t

41 NSAIDs interact with phospholipids and uncouple mitochondrial oxidative phosp

42 rs of which hydrolyze nucleoside phosphates, phospholipids, and other related molecules.

43 ll as insoluble lipid surfactants, including phospholipids, and proteins, a composition similar to pu

44 Phosphatidylcholines are major myelin phospholipids, and several phosphorylated phosphatidylin

45 hat an engineered opsin monomer can scramble phospholipids, and that the lipid-exposed face of TM4 is

46 Dmpw), indicating the importance of lipid-, phospholipid-, and protein-water partitioning.

47 n autoantibodies, such as anti-NMDAR or anti-phospholipid antibodies, promote CNS lupus.

48 f GM1-containing NDs prepared with the three phospholipids are found to be similar in magnitude, indi

49 How phospholipids are trafficked between the bacterial inner

50 Such flows result in redistribution of phospholipid at the cell surface and actomyosin in the c

51 an oblate orientational distribution of the phospholipids at a peptide/lipid ratio of 1:5.

52 yer perturbation effects of the two oxidized phospholipids based on the chemical identities of their

53 hereby facilitating transbilayer exchange of phospholipids between the leaflets of the vesicle membra

54 reports the distribution coefficient between phospholipid bilayer membranes and phosphate buffered sa

55 itations by reconstituting unlabeled LeuT in phospholipid bilayer nanodiscs, subjecting them to hydro

56 a(2+), reconstituted OmpLA diffused within a phospholipid bilayer without revealing any signs of phos

57 veals similarities in thickness to a typical phospholipid bilayer.

58 rtion of integral membrane proteins into the phospholipid bilayer.

59 ations of transport across electropores in a phospholipid bilayer.

60 serted via a ring of membrane anchors into a phospholipid bilayer.

61 lasma membrane and after reconstitution into phospholipid bilayer.

62 he membrane interactions of the peptide with phospholipid bilayers and its membrane topology using st

63 These results suggest that supported fluid phospholipid bilayers are not homogenous at the nanoscal

64 tack bacterial membranes and upon landing on phospholipid bilayers instantaneously (seconds) convert

65 -length and truncated constructs of CXCR1 in phospholipid bilayers under physiological conditions.

66 holesterol-binding site of the M2 protein in phospholipid bilayers using solid-state NMR spectroscopy

67 o its affinity toward the acyl chains in the phospholipid bilayers.

68 n homology domain mutants exhibited enhanced phospholipid binding.

69 f1 requires both its ubiquitin-ligase and C2 phospholipid-binding domains, and involves K48- rather t

70 ive factor attachment protein receptor)- and phospholipid-binding protein that localizes to and prime

71 Here, we report that the phospholipid-binding protein, annexin A2 (ANXA2) functio

72 ersistent presence of autoantibodies against phospholipid-binding proteins (aPLs), such as beta2 glyc

73 important mechanism that couples the rate of phospholipid biosynthesis and endomembrane biogenesis to

74 epressor Opi1p, which controls expression of phospholipid biosynthesis genes, but the mechanisms cond

75 e phosphocholine, an important precursor for phospholipid biosynthesis in diverse organisms.

76 sis of PA, a central metabolite for membrane phospholipid biosynthesis.

77 r characterize the ER subdomain, we screened phospholipid biosynthetic enzymes and found that the aut

78 The induction of phospholipid biosynthetic genes is accompanied by induct

79 BR scrambles fluorescent analogues of common phospholipids but does not transport a glycosylated diph

80 ight chain), and two C2-domains that bind to phospholipids, Ca(2+) and SNAREs.

81 Moreover, the mitochondria-specific phospholipid, cardiolipin, was significantly reduced in

82 idine metabolism, fatty acid beta-oxidation, phospholipid catabolism, arachidonic acid and linoleic a

83 species, including di- and triacylglycerols, phospholipids, cholesteryl esters, and wax esters in OG-

84 he three-dimensional spatial distribution of phospholipid classes, phosphatidylcholine (PC), phosphat

85 t, and reversible fashion but did not affect phospholipid clearance.

86 MBs), consisting of an oxygen gas core and a phospholipid coating functionalised with Rose Bengal (RB

87 We further investigated three phospholipids commonly found in lipid membranes, phospha

88 ilitate P acquisition and the degradation of phospholipids compared with other stramenopiles.

89 on the plasma membrane, and actively exports phospholipid complexes from the cytoplasmic to the exocy

90 Mammalian cell membranes have different phospholipid composition and cholesterol content, displa

91 RBCs or plasma, but was associated with the phospholipid composition of the RBC membranes and with p

92 cteristic of the OM is lipid asymmetry, with phospholipids comprising the inner leaflet and lipopolys

93 min increases alanine levels and reduces the phospholipid content in very large HDL particles.

94 After the 4-month treatment, the phospholipid content of very large HDL was lower in metf

95 lar levels of citrate, the ratio of ATP/ADP, phospholipid content, and ATP citrate lyase expression.

96 bilayer, but the subsequent realization that phospholipids could also serve as second messengers brou

97 erein for the first time, join other complex phospholipid defects that cause leukoencephalopathies in

98 h free 9-cis-retinal from Rho in an in vitro phospholipid/detergent bicelle system.

99 ion of purified rhodopsin reconstituted into phospholipid/detergent bicelles with rhodopsin reconstit

100 Since seedlings deficient in PHOSPHOLIPID:DIACYLGLYCEROL ACYLTRANSFERASE1 (PDAT1) wer

101 itol-4,5-bisphosphate (PIP2), one of the key phospholipids, directly interacts with several membrane

102 stems we investigated DNA oligomers (3-HPA), phospholipids (dithranol, THAP, HABA), and non-covalent

103 biomimetic membranes prevented formation of phospholipid domains that regulate enzyme activity.

104 brane solubilization of a negatively charged phospholipid (DPhPG) with the motivation of creating bio

105 wn-regulation of synj1 rescues blast-induced phospholipid dysregulation and prevents development of T

106 s oxidative modification of lipoproteins and phospholipids, endothelial cell activation, and macropha

107 ation, suggests that Al reacts with membrane phospholipids, enhancing intracellular transport of meta

108 retain activity in detergent extracts) that phospholipid environment is a strong determining factor

109 re extracted with food grade ethanol and egg phospholipids (ePL) produced by deoiling with acetone.

110 Moreover, we show that Vps13 binds phospholipids, especially phosphatidylinositol 3-phospha

111 peutic potential of the clinical-grade alkyl-phospholipid ether analog CLR1404, 18-(p-iodophenyl)octa

112 ramblase that facilitates rapid transbilayer phospholipid exchange in liposomes.

113 gical processes, including lipid metabolism, phospholipid exchange, metabolite transport, signaling,

114 M4 is unlikely to contribute to transbilayer phospholipid exchange.

115 -terminal helix; (iii) the energy barrier of phospholipid extraction from the membrane is lowered by

116 s in both bacterial ( 51%) and fungal ( 58%) Phospholipid Fatty Acids (PLFA) biomass.

117 enriched (13)C from fullerol into microbial phospholipid fatty acids (PLFA) we also report, for the

118 cted at the seafloor by quantifying sediment phospholipid fatty acids (PLFAs) and their carbon stable

119 kers.We aimed to assess the utility of serum phospholipid fatty acids (PLFAs) as biomarkers of dietar

120 oids, tocopherols, folate, vitamin B-12, and phospholipid fatty acids, were collected at the beginnin

121 microbial tissue was examined in biomass and phospholipid fatty acids.

122 P4-ATPases, also known as phospholipid flippases, are responsible for creating and

123 ow pH and the presence of negatively charged phospholipids for maximal binding.

124 in controlling the levels of polyunsaturated phospholipids for the proper functioning of cell membran

125 orter at blood brain barrier is specific for phospholipid form of DHA.

126 ts can cooperate to extract large numbers of phospholipids from the membrane bilayer.

127 to mediate retrograde transport of misplaced phospholipids from the outer leaflet of the OM to the cy

128 in baboons infused with factor Xa (FXa) and phospholipids (FXa/phosphatidylcholine-phosphatidylserin

129 MP), an important but low-abundance class of phospholipids, has been hindered due to its difficulties

130 We conclude that polyunsaturated phospholipids have been largely overlooked as major play

131 ractions as well as hydrogen bonding between phospholipid head groups and amine groups of chitosan.

132 ng the membrane surface interacting with the phospholipid head groups.

133 amine further limited its interactions with phospholipid head-groups to facilitate pseudopilin membr

134 ta suggest that ApoE proteins regulate brain phospholipid homeostasis in response to TBI and that the

135 tochondrial PC synthesis pathway to cellular phospholipid homeostasis, and establish the importance o

136 tical role for ER-localized Psd1 in cellular phospholipid homeostasis, question the significance of a

137 associated with increased oxidative stress, phospholipid hydrolysis and energy depletion that are ch

138 he amino acid cysteine, or by inhibiting the phospholipid hydroperoxidase glutathione peroxidase 4 (G

139 l and an exchangeable mimic of a low-melting phospholipid in liquid-disordered bilayers can be much s

140 and an exchangeable mimic of a high-melting phospholipid in liquid-ordered bilayers.

141 maintenance of sufficiently high amounts of phospholipid in the Salipro nanoparticle to mimic a real

142 yceride species and a subsequent decrease in phospholipids in cART/HIV-1-exposed infants compared to

143 re for the high-throughput identification of phospholipids in data acquired by LC-MS and shotgun expe

144 ine, constitutes more than half of the total phospholipids in eukaryotic cell membranes.

145 To compensate for low phospholipids in exponential growth, N. oceanica synthes

146 This paper presents a method for determining phospholipids in soybean lecithin samples by phosphorus

147 and lower levels of cardiolipin, among other phospholipids in the apical plasma membrane compared to

148 olysaccharide (LPS) in the outer leaflet and phospholipids in the inner leaflet.

149 d virus infections by specifically targeting phospholipids in the lipid bilayer via the production of

150 The determined concentrations of phospholipids in the samples varied between 38.1 and 45%

151 ith increased cholesterol, triglycerides and phospholipids, in WT, but not TRPC5 KO mice.

152 lipase A2 activity that acts on the membrane phospholipids, including the phosphoinositides, to form

153 oconvertible tag (for lamin B1) and membrane phospholipid incorporation using stable isotope labellin

154 Interaction with acidic phospholipids induces structure, but its disposition whe

155 demonstrating polar-lipid, and specifically phospholipid, inhibition of prion-seeded amyloid formati

156 The crystal structure of a designed phospholipid-inspired amphiphilic phosphopeptide at 0.8

157 RAL specifically to 11cRAL through a retinyl-phospholipid intermediate in photoreceptor membranes.

158 experiments, LIMP-2 facilitates transport of phospholipids into murine fibroblasts, with a strong sub

159 h anchors when aggregated to sort subsets of phospholipids into nanoclusters with defined lipid compo

160 This anionic phospholipid is restricted almost exclusively to the inn

161 gh a non-enzymatic process involving retinyl-phospholipids.It is currently thought that visual pigmen

162 dylinositol phosphate kinase (PIPKIgamma), a phospholipid kinase generating PIP2, is positively expre

163 a-3) essential fatty acid (EFA) supplements, phospholipid (krill oil) and triacylglyceride (fish oil)

164 cholesterol, XL-HDL-free cholesterol, XL-HDL phospholipids, L-HDL cholesterol, and L-HDL-free cholest

165 on to the apolipoprotein, insertion into the phospholipid layer, and loading into the core.

166 high triglycerides in mammary gland to high phospholipid levels in tumors.

167 metry further identified specific effects on phospholipids linked to both neural development and neur

168 spholopion-90H and 80H) and non-hydrogenated phospholipids (Lipoid-S100) in combination with choleste

169 fy oxidized lipids (glycerides, fatty acids, phospholipids, lysophospholipids, and galactolipids) and

170 3-benzoxadiazol-4-y l)], incorporated into a phospholipid membrane bilayer supported on 3 mum silica

171 GTPase-driven actin polymerization at model phospholipid membrane bilayers in cell-free extracts and

172 e show results of the membrane dynamics of a phospholipid membrane multilayer-stack on a solid substr

173 r the ceramide moiety nor the surface of the phospholipid membrane plays a significant role in CTB5 b

174 cs simulations of a BR trimer in an explicit phospholipid membrane revealed water penetration along t

175 onstrate the suitability of a size-adaptable phospholipid membrane-mimetic system for solution NMR st

176 When detergents and phospholipid membranes are dispersed in aqueous solution

177 ch to measure dynamic membrane properties of phospholipid membranes close to an interface.

178 he association of the PLA2R-A2t complex with phospholipid membranes in vitro.

179 vation of the hitherto invisible property of phospholipid membranes using neutrons.

180 or regulation of Opi1p localization and thus phospholipid metabolism in yeast.

181 These findings suggest that phospholipid metabolism is linked to the cell cycle and

182 decarboxylases (PSDs) are central enzymes in phospholipid metabolism that produce phosphatidylethanol

183 novel function of PPARdelta in regulation of phospholipid metabolism through LPCAT3.

184 The UPR has long been known to regulate phospholipid metabolism, and Lpl1's relationship with Ha

185 istinct proteotoxic stress responses control phospholipid metabolism.

186 isorder is linked to highly altered membrane phospholipid metabolism.

187 se include altered calcium, cholesterol, and phospholipid metabolism; altered mitochondrial dynamics;

188 f GPC+PC suggest alterations in the membrane phospholipids metabolism in bipolar disorder.

189 sults suggest greater alteration of membrane phospholipid metabolisms in rapid cycling BD-I compared

190 zation due to favorable Gibbs free energy of phospholipid mixing.

191 palmitoyl-sn-glycero-3-phosphocholine (DPPC) phospholipid mixtures using quartz crystal microbalance-

192 high sensitivity to the spatial proximity of phospholipid molecules near the sensor surface, the LSPR

193 degraded the membrane with a turnover of 2 phospholipid molecules per second and per OmpLA dimer un

194 proteins that associate with the bounding LD phospholipid monolayer.

195 e of model membranes represented by Langmuir phospholipid monolayers and Aerosol-OT (AOT) reverse mic

196 n micelles of dodecyl maltoside (DDM) and in phospholipid nanodiscs by monitoring the spatial positio

197 re, we present a protocol on the assembly of phospholipid nanodiscs of various sizes for structural s

198 Phospholipid nanogels enhance the stability and performa

199 Phospholipid nanovesicles were developed to improve the

200 Phospholipids occurring in cell membranes and lipoprotei

201 idylcholine (PC), the most abundant cellular phospholipid, occurs redundantly via the ER-localized Ke

202 Cardiolipin (CL), the signature phospholipid of mitochondrial membranes, is important fo

203 Cardiolipin (CL), the signature phospholipid of mitochondrial membranes, plays an import

204 re was no difference in the total amounts of phospholipids of each class, we revealed that the levels

205 The influence of two bioactive oxidized phospholipids on model bilayer properties, membrane pack

206 The effect of hydrogenation of phospholipids on the characteristics of freeze-dried lip

207 monstrate that exposure of HAECs to oxidized phospholipids or pro-inflammatory cytokines results in s

208 circulation of a specific group of oxidized phospholipids (oxPCCD36) that are ligands for the platel

209 and lipoproteins are converted into oxidized phospholipids (OxPL) by oxidative stress promoting ather

210 In particular, oxidized phospholipids (OxPls) formed under intracellular stress

211 e to seek other, non-signaling functions for phospholipids, particularly in their interactions with m

212 may interact positively with EVOO to inhibit phospholipid peroxidation, and thus, McPC-EEVOO could be

213 ockout mice lacking the LPA-degrading enzyme phospholipid phosphate phosphatase type 1 (PLPP1) had a

214 rge lipids up to m/z of 1000, including lyso-phospholipid, phosphatidic acid (PA), phosphoethanolamin

215 haliana stimulates biosynthesis of the major phospholipid phosphatidylcholine (PC) and causes expansi

216 suppress the signals from the most abundant phospholipids (phosphatidylcholine (PC) and phosphatidyl

217 grees with markers for the anionic signaling phospholipids phosphatidylinositol 4,5-bisphosphate and

218 ed by diverse stimuli, including the anionic phospholipid phosphatidylserine.

219 Moreover, 71 sulfatides and 59 polar phospholipids (phosphatidylserines, phosphatidylinositol

220 phosvitin and lipovitellin from egg yolk and phospholipids/phosphopeptides from human serum.

221 ormal WHAMM function involved binding to the phospholipid PI(3)P and promoting actin nucleation at na

222 otably, both activators require the membrane phospholipid PIP2 but appear to interact independently w

223 Methylation of phospholipids (PL) leads to increased uniformity in posi

224 r in different lipid compartments, including phospholipids, plasma, cholesterol esters, and adipose t

225 isruptions in membrane structure by oxidized phospholipids play a role in the regulation of overall e

226 d a rapid and progressive change in membrane phospholipid polarity, manifested as phosphatidylserine

227 acted considerable attention because it is a phospholipid precursor, a lipid second messenger, and a

228 d in both positive- and negative-ion mode to phospholipids present in human serum, and the data set w

229 otentially targeting domain organization and phospholipid-protein binding, which has implications for

230 The novel phospholipid-recycling scheme opens new avenues for meta

231 ith meiosis II progression, concomitant with phospholipid remodeling.

232 Furthermore, induction of the phospholipid-remodeling enzyme LPCAT3 in response to liv

233 evious findings that all three proteins bind phospholipids, results presented here indicate that mult

234 ins, which form a nucleational core with the phospholipid-rich membrane and support the formation of

235 Phospholipid saturated fatty acids and monounsaturated f

236 a protein functioning as a Ca(2+)-dependent phospholipid scramblase and Ca(2+)-activated chloride ch

237 The G protein-coupled receptor opsin is a phospholipid scramblase that facilitates rapid transbila

238 ruption of this asymmetry by ATP-independent phospholipid scrambling is important in cellular signali

239 Phospholipid scrambling significantly alters the physica

240 ysiological implications of Ca(2+)-dependent phospholipid scrambling, the extracellular vesicles asso

241 at they are produced by PAF-AH2, an oxidized-phospholipid-selective phospholipase A2.

242 bolite classes and study groups-for example, phospholipids showed maximal difference at 5:00 AM (lean

243 injured neurons, is dependent on exposure of phospholipid signals, and is achieved through the balanc

244 ne, and we observed that the upregulation of phospholipid species and cholesterol is correlated with

245 From bacteria to mammals, different phospholipid species are segregated between the inner an

246 Phosphatidylethanolamine (PE) is a major phospholipid species with important roles in membrane tr

247 athway, and lipogenesis, including primarily phospholipids, sphingolipids, and bile acids.

248 We further found that phospholipids, sphingolipids, and other membrane lipids

249 The phospholipid stability increased by a factor of 33.6%, 3

250 or hydrolysis of arachidonic acid containing phospholipid substrates releasing free arachidonic acid

251 asic surface that can associate with anionic phospholipids such as phosphatidylserine.

252 ation and active provision of a procoagulant phospholipid surface enriched in 12/15-lipoxygenase-deri

253 analyses showed that LPIN1 knockdown blocks phospholipid synthesis and changes membrane lipid compos

254 Spatial organization of phospholipid synthesis in eukaryotes is critical for cel

255 Lipin-1 regulation of phospholipid synthesis maintains endoplasmic reticulum h

256 P) controlling the rate-limiting step in the phospholipid synthesis pathway, is highly up-regulated i

257 ppears to reflect Hac1's role in stimulating phospholipid synthesis under stress.

258 controls the expression of PSS for membrane phospholipid synthesis.

259 pression and activity of enzymes involved in phospholipid synthesis.

260 Phospholipid ternary systems are useful model systems fo

261 ing the IDO inhibitor, indoximod (IND), to a phospholipid that allows prodrug self-assembly into nano

262 hosphate (PI(4,5)P2) is a negatively charged phospholipid that plays a major role in recruiting and r

263 ding energy of the LC phase of the saturated phospholipids that are common to all natural and clinica

264 detected regional increases in ether-linked phospholipids that are the precursors of PAF, and global

265 Phosphoinositides (PIs) are phospholipids that perform crucial cell functions, rangi

266 les have been assembled and coassembled from phospholipids, their modified versions, and other single

267 y, whereby it transfers an acyl chain from a phospholipid to the amine group of the N-terminal cystei

268 lipids to the pore, but allows outer leaflet phospholipids to bind to a pronounced ridge surrounding

269 drial enzyme that transfers fatty acids from phospholipids to lysophospholipids.

270 hown to charge-invert the positively charged phospholipids to the negative mode.

271 rchitecture prevents access of inner leaflet phospholipids to the pore, but allows outer leaflet phos

272 Although the phospholipid transfer protein Stard7 promotes uptake of

273 alpha-helical OM protein that functions as a phospholipid translocation channel, forming a 20-A-thic

274 rins do not appear to play an active role in phospholipid transport.

275 Our results suggest that the phospholipid transporter activity of ALA1/ALA2 may be ne

276 the likely importance of these hepatobiliary phospholipid transporter genes in the pathology of gallb

277 ifferent approach and mimic the synthesis of phospholipids using abiotic but highly selective bioconj

278 e was studied in the absence and presence of phospholipids using Langmuir films, polarization modulat

279 Phospholipid variants determine membrane properties such

280 the gel-to-fluid phase transition in a pure phospholipid vesicle was observed to take place across a

281 chloride-selective permeability to preformed phospholipid vesicles and that this selectivity is stron

282 Using phospholipid vesicles as a model system, we observe that

283 introduction of linoleic acid, via fusion of phospholipid vesicles to mitochondria isolated from DHA-

284 Kd was not altered either by the presence of phospholipid vesicles, phosphatidylinositol 4,5-bisphosp

285 n which dimerizes en route to insertion into phospholipid vesicles, QUAD opsin reconstitutes as a mon

286 confirmed that ApoL1 stably associates with phospholipid vesicles, requiring low pH and the presence

287 of cytochrome c with cardiolipin-containing phospholipid vesicles, serving as models of the OMM, is

288 he committed step for the synthesis of major phospholipids via the CDP-diacylglycerol pathway.

289 poration of very-long-chain fatty acids into phospholipids, we separately examined the effects of lys

290 About 1% of the phospholipids were found to be detached from the SSLM be

291 d per OmpLA dimer until most of the membrane phospholipids were hydrolyzed and the protein became tig

292 Overall, the properties of native egg phospholipids were significantly enhanced in a potential

293 In the 1970s, phospholipids were still considered mere building blocks

294 laboratory, where both membrane proteins and phospholipids were the foci of study, thus providing a j

295 s, much less is known about the synthesis of phospholipids, which is essential for membrane biogenesi

296 e acyl moiety region between the bilayers of phospholipids, which results in ER-LD swelling.

297 The main lipid components are phospholipids, which vary in acyl chain length, saturati

298 Cardiolipin (CL) is a dimeric phospholipid with critical roles in mitochondrial bioene

299 It binds to several membrane-resident phospholipids with preference for phosphatidylinositol m

300 f mutants that disrupt Tau interactions with phospholipids without interfering with its ability to fo