ライフサイエンスコーパス: phosphatidylglycerol

1 eoyl phosphatidylglycerol; DMPG, dimyristoyl phosphatidylglycerol).

2 chain composition of phosphatidylcholine and phosphatidylglycerol.

3 rms oligomeric pores on membranes containing phosphatidylglycerol.

4 sphatidylethanolamine, phosphatidylserine or phosphatidylglycerol.

5 r by phosphate-masked phosphatidylcholine or phosphatidylglycerol.

6 from 0 to 8 mol % PS and similar amounts of phosphatidylglycerol.

7 om Escherichia coli is preloaded with PA and phosphatidylglycerol.

8 lipids of the cytoplasmic membrane, such as phosphatidylglycerol.

9 ly esterified to the sn-2 glyceryl carbon of phosphatidylglycerol.

10 the nonreducing end following initiation on phosphatidylglycerol.

11 membranes contained phosphatidylcholine and phosphatidylglycerol.

12 alpha-synuclein is clustered are enriched in phosphatidylglycerol.

13 ructure in the micelles of SDS or dioctanoyl phosphatidylglycerol.

14 but did not decrease the relative amount of phosphatidylglycerol.

15 ipin-deficient mutant were characteristic of phosphatidylglycerol.

16 in demonstrated the presence of glycosylated phosphatidylglycerol.

17 tween the peptide and short chain dioctanoyl phosphatidylglycerol.

18 otropic phase in anionic bilayers containing phosphatidylglycerol.

19 rol to phospholipase D2 for the synthesis of phosphatidylglycerol.

20 nsion and identified them as cardiolipin and phosphatidylglycerol.

21 olipids in the presence of glycerol to yield phosphatidylglycerol.

22 d bacterial membrane cardiolipin and reduced phosphatidylglycerol.

23 phatidylglycerol phosphate (PGP) to generate phosphatidylglycerol.

24 hydrolyzes CL, phosphatidylethanolamine, and phosphatidylglycerol.

25 "group 2" capsular polysaccharides to (lyso)phosphatidylglycerol.

26 iously characterized dNKT cell Ag, mammalian phosphatidylglycerol.

27 which occurs by binding surface disaturated phosphatidylglycerols.

28 mass spectrometry are a group of disaturated phosphatidylglycerols.

29 and a mixture of POPC/POPG (palmitoyl-oleyl-phosphatidylglycerol) (4:1) lipids.

30 verts phosphatidylglycerolphosphate (PGP) to phosphatidylglycerol, a critical step in the de novo bio

31 iated by the reduction in bacterial membrane phosphatidylglycerol, a previously undescribed bacterial

32 taS) polymerizes polyglycerol-phosphate from phosphatidylglycerol, a reaction that is essential for t

33 of poly-Kdo linker assembly on a fluorescent phosphatidylglycerol acceptor.

34 lated galactolipids, and head-group-acylated phosphatidylglycerol (acPG), sulfoquinovosyldiacylglycer

35 With 10% of the anionic dioleoyl phosphatidylglycerol added to dioleoyl phosphatidylethan

36 lacement studies revealed that the microbial phosphatidylglycerol Ag binds significantly better to CD

37 Synthetic cardiolipin or phosphatidylglycerol also induced pulmonary hypertension

38 ced by RNAi in the ats1-1 mutant background, phosphatidylglycerol amounts decreased, leading to a gro

39 ynthesis and translocation of membrane lysyl-phosphatidylglycerol (an mprF-dependent function) was su

40 hatidylethanolamine, diphosphatidylglycerol, phosphatidylglycerol and an unidentified aminophospholip

41 ut was rather caused directly by the lack of phosphatidylglycerol and cardiolipin in mitochondrial me

42 s, which contain only anionic phospholipids (phosphatidylglycerol and cardiolipin), green fluorescent

43 er phospholipids derived from phosphatidate, phosphatidylglycerol and cardiolipin, were also depleted

44 n contrast, the outer leaflet is enriched in phosphatidylglycerol and cardiolipin, which show a marke

45 g concentration of the anionic phospholipids phosphatidylglycerol and cardiolipin.

46 UE54, lacks the major anionic phospholipids phosphatidylglycerol and cardiolipin.

47 s1Delta) of Saccharomyces cerevisiae lacking phosphatidylglycerol and cardiolipin.

48 fferentiate between the roles of monoanionic phosphatidylglycerol and dianionic cardiolipin (CL) in t

49 cinerea revealed decreases in the levels of phosphatidylglycerol and digalactosyldiacylglycerol, sug

50 n baseline separate the cis-trans isomers of phosphatidylglycerol and phosphatidylcholine (PC) with t

51 tory difference in cardiolipin, decreases in phosphatidylglycerol and phosphatidylethanolamine, and t

52 alysis identified the ligand as a mixture of phosphatidylglycerol and phosphatidylethanolamine.

53 rucial for gametogenesis and biosynthesis of phosphatidylglycerol and phosphatidylinositol in the end

54 analysis in the knockdown lines showed that phosphatidylglycerol and phosphatidylinositol metabolism

55 t study, we determined that palmitoyl-oleoyl-phosphatidylglycerol and phosphatidylinositol, which are

56 that P2X7 channel activity is facilitated by phosphatidylglycerol and sphingomyelin, but dominantly i

57 ociated transcript levels were higher, while phosphatidylglycerol and sulfolipid levels were lower th

58 ty interactions between the palmitoyl-oleoyl-phosphatidylglycerol and the Toll-like receptor 4-intera

59 re similar, but in FtsA samples longer chain phosphatidylglycerols and phosphatidylethanolamines were

60 ed composition (3:1 phosphatidylethanolamine:phosphatidylglycerol) and examined channel activity usin

61 ctanoyl phosphatidylglycerol, and didecanoyl phosphatidylglycerol) and four lipid-mimicking anionic d

62 iposomes (containing phosphatidylcholine and phosphatidylglycerol) and four types of animal/human cel

63 of bacterial (phosphatidylethanolamine (PE)/phosphatidylglycerol) and mammalian (phosphatidylcholine

64 ation, such as pure phosphatidylserine, pure phosphatidylglycerol, and asolectin.

65 he acidic phospholipids, phosphatidylserine, phosphatidylglycerol, and cardiolipin, but not phosphati

66 (dihexanoyl phosphatidylglycerol, dioctanoyl phosphatidylglycerol, and didecanoyl phosphatidylglycero

67 We identified phosphatidic acid, phosphatidylglycerol, and glycerol phosphate as specific

68 sphatidylmethanol (PMe), phosphatidylserine, phosphatidylglycerol, and phosphatidic acid] interfaces

69 pids, phosphatidic acid, phosphatidylserine, phosphatidylglycerol, and phosphatidylinositol, were fou

70 te, dodecyl phosphocholine, lyso 1-palmitoyl phosphatidylglycerol, and phospholipid vesicles).

71 aturated pulmonary surfactant phospholipids; phosphatidylglycerols, and phosphatidylcholines.

72 n mutant is unable to synthesize lysinylated phosphatidylglycerols, and this defect is rescued by gen

73 ceptors bind to both dihydrogenphosphate and phosphatidylglycerol anions in a similar binding motif.

74 y revealed that phosphatidylethanolamine and phosphatidylglycerol are depleted in endovesicles while

75 c phospholipid cardiolipin and its precursor phosphatidylglycerol are synthesized and localized in th

76 ine and histidine, and phosphatidic acid and phosphatidylglycerol are the least basic of the six lipi

77 Phosphatidylglycerols are induced by gut dysbiosis and i

78 dylinositols, lysophosphatidylinositols, and phosphatidylglycerols) are detected within a 15 min run.

79 preferential enrichment of the anionic lipid phosphatidylglycerol around the cationic KALP peptide in

80 We identified Listeria phosphatidylglycerol as a microbial Ag that was signific

81 are Mn(2+) -dependent metal enzymes that use phosphatidylglycerol as a substrate.

82 ve analysis indicated phosphatidic acids and phosphatidylglycerols as the most abundant species, both

83 Phosphatidylglycerol, as a bioactive lipid, could potent

84 sphatidylethanolamine, phosphatidylserine or phosphatidylglycerol, as well as at internal sites: lysi

85 uestion of whether an alternative pathway of phosphatidylglycerol assembly in the plastid exists.

86 phatidylglycerol was distinct from mammalian phosphatidylglycerol because it contained shorter, fully

87 their GB values, with phosphatidylserine and phosphatidylglycerol being the most acidic.

88 Using melittin and a dipalmitoyl phosphatidylglycerol bilayer as a model system, we monit

89 chloline)/DMPG (1,2-dimyristoyl-sn-glycero-3-phosphatidylglycerol) bilayer, consistent with neutron d

90 opically symmetric or asymmetric dipalmitoyl phosphatidylglycerol bilayers during their interaction w

91 l 2-naphtho[2,1-b]furan-1-ylacetate] blocked phosphatidylglycerol binding to LtaS and inhibited LTA s

92 The inhibitors had no effect on phosphatidylglycerol biosynthesis or CRD1 gene expressio

93 mutant deficient in a late step of plastidic phosphatidylglycerol biosynthesis.

94 o liposomes containing phosphatidylserine or phosphatidylglycerol, but not the basic or neutral phosp

95 oline (C(16:0)C(18:1)PC) and palmitoyloleoyl-phosphatidylglycerol (C(16:0)C(18:1)PG).

96 We show here that the phospholipid phosphatidylglycerol can inhibit the activation of toll-

97 negatively charged phospholipids, including phosphatidylglycerol, can also support TRPV1 activity in

98 phospholipids, including phosphatidylserine, phosphatidylglycerol, cardiolipin, phosphatidic acid, an

99 ation characteristics were favorable for the phosphatidylglycerol chlorohydrins, and they were theref

100 osphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, cholesterol) were constructed.

101 It was hypothesized that the phosphatidylglycerol component of surfactant was inhibit

102 that an exogenous surfactant, with a reduced phosphatidylglycerol composition would increase peptide

103 Although diluting the phosphatidylglycerol content in an existing surfactant,

104 t osmotic stress in membranes with increased phosphatidylglycerol content, i.e. in intact C. glutamic

105 Additionally, 23% reduction in phosphatidylglycerol content, the immediate biosynthetic

106 activities in conjunction with a decrease in phosphatidylglycerol content.

107 nal studies to determine how polyunsaturated phosphatidylglycerols contribute to esophageal carcinoge

108 Negatively charged phosphatidylglycerol could also induce heat activation o

109 actions of 10 or 20% to membranes containing phosphatidylglycerol, daptomycin no longer forms pores o

110 osphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, digalactosyldiacylglycerol, monoga

111 zero) were observed for phosphatidylcholine, phosphatidylglycerol, dihydrosphingomyelin, and cardioli

112 Three anionic phospholipids (dihexanoyl phosphatidylglycerol, dioctanoyl phosphatidylglycerol, a

113 only the crd1-null mutant, which accumulates phosphatidylglycerol, displays significant mitochondrial

114 DG, and SQDG) and phospholipids dilinolenoyl-phosphatidylglycerol (DLPG), 1,2-dioleoylphosphatidylgly

115 lcholine (DMPC)/1,2-dimyristoyl-sn-glycero-3-phosphatidylglycerol (DMPG) and 1-palmitoyl-2-oleoyl-sn-

116 the negatively charged lipid (DOPG, dioleoyl phosphatidylglycerol; DMPG, dimyristoyl phosphatidylglyc

117 ) doped with both negatively charged dioleyl phosphatidylglycerol (DOPG), and zwitterionic dioleyl ph

118 er component, in combination with distearoyl phosphatidylglycerol (DSPG) and cholesterol, were more s

119 ion of the positively charged lysyl-dioleoyl-phosphatidylglycerol exclusively on the cytoplasmic faci

120 ly charged lipids like phosphatidylserine or phosphatidylglycerol for activity.

121 st prevalent native anionic lipid headgroup; phosphatidylglycerol for EmrE and phosphatidylinositol f

122 A synthetic phosphatidylglycerol-free surfactant however, was shown

123 ased on these in vitro experiments synthetic phosphatidylglycerol-free surfactants seem optimal for d

124 -containing phosphatidylinositol (GPIns) and phosphatidylglycerol (GPGro) species.

125 units of sn-glycerol-1-P groups derived from phosphatidylglycerol head groups.

126 module and the lysyl moiety anchored to the phosphatidylglycerol headgroup.

127 Intact polar lipids with phosphatidylglycerol headgroups and glycerol dibiphytany

128 ction of this 16:1 (Delta3trans) -containing phosphatidylglycerol in chloroplasts has remained elusiv

129 tion, with the fraction of the anionic lipid phosphatidylglycerol in neutral, phosphatidylcholine mem

130 choic acids, (ii) the incorporation of lysyl-phosphatidylglycerol in the bacterial membrane and a con

131 (iii) Phosphatidylglycerol in the membrane of C. glutamicum se

132 Its action requires both calcium and phosphatidylglycerol in the target membrane, and it is a

133 lowing for effective competition for anionic phosphatidylglycerols in bacterial membranes.

134 chment of the anionic lipids cardiolipin and phosphatidylglycerol, indicating their close proximity t

135 Phosphatidylglycerol is elevated in crd1 Delta mutant ce

136 , with a membrane comprised predominantly of phosphatidylglycerol, is viable and grows at near-wild-t

137 hermore, by using gold nanorods covered with phosphatidylglycerol layers and single particle spectros

138 Remarkably, phosphatidylglycerol levels decreased with increasing ph

139 We have resolved a phosphatidylglycerol lipid associated with McjD at 3.4 A

140 cally to liposomes containing anionic diacyl phosphatidylglycerol lipids (PG); however, the ITC data

141 roup negative charge through the addition of phosphatidylglycerol lipids favours protein reconstituti

142 RTD-1 to anionic bilayers containing PC and phosphatidylglycerol lipids induces much greater orienta

143 he E. coli ammonium transporter AmtB prefers phosphatidylglycerol lipids overall but has a minor affi

144 structural studies have revealed binding of phosphatidylglycerol lipids to functional important part

145 bundance of diglycerides, triglycerides, and phosphatidylglycerol lipids.

146 3 NS4B was reconstituted into lyso-myristoyl phosphatidylglycerol (LMPG) micelles.

147 Further, although mammalian phosphatidylglycerol-loaded CD1d tetramers did not stain

148 d not stain dNKT cells, the Listeria-derived phosphatidylglycerol-loaded tetramers did.

149 yl-phosphatidic acid or 1-palmitoyl-2-oleoyl-phosphatidylglycerol (</=15 mol %) in C1P source vesicle

150 The present data indicate that phosphatidylglycerol may anchor the type 3 polysaccharid

151 binding of IM30 rings to negatively charged phosphatidylglycerol membrane surfaces results in a high

152 ylcholine/1-palmitoyl-2-oleoyl-sn-gl ycero-3-phosphatidylglycerol) membranes.

153 (MG2a) and PGLa in phosphatidylethanolamine/phosphatidylglycerol mimics of Gram-negative cytoplasmic

154 que glycolipid terminus consisting of a lyso-phosphatidylglycerol moiety with a beta-linked poly-(3-d

155 Arabidopsis thaliana missing this particular phosphatidylglycerol molecular species lacks the necessa

156 d species, 17 species of oxylipin-containing phosphatidylglycerols, monogalactosyldiacylglycerols (MG

157 toylphosphatidylcholine and palmitoyl-oleoyl-phosphatidylglycerol monolayers.

158 holine, disaturated phosphatidylcholine, and phosphatidylglycerol more than 5% rat serum alone.

159 sphatidylinositol, is minimally activated by phosphatidylglycerol or phosphatidylethanolamine (PE), a

160 n of phosphatidylcholine bilayers containing phosphatidylglycerol or PI(4,5)P2.

161 Diacyl forms of PE, phosphatidylglycerol, or the tetra-acylated form of card

162 mined in fluid-phase 3:1 phosphatidylcholine/phosphatidylglycerol (PC/PG) and 1:1 phosphatidylethanol

163 rol (PC/PG) and 1:1 phosphatidylethanolamine/phosphatidylglycerol (PE/PG) bilayers to identify molecu

164 In mixtures of phosphatidylcholine (PC)/phosphatidylglycerol (PG) 50:50 and 70:30, release of co

165 Sin a 2 and Ara h 1 bind phosphatidylglycerol (PG) acid but not phosphatidylcholi

166 imilar proton relay capability as the native phosphatidylglycerol (PG) analog lipids in the purple me

167 cking the committed step in the synthesis of phosphatidylglycerol (PG) and cardiolipin (CL), which we

168 d recipients have heretofore been defined as phosphatidylglycerol (PG) and cardiolipin.

169 s of the mitochondrial anionic phospholipids phosphatidylglycerol (PG) and CL.

170 Lipid profiling revealed that 34C species of phosphatidylglycerol (PG) and monogalactosyl diacylglyce

171 neous curvature, with the negatively charged phosphatidylglycerol (PG) and neutrally charged phosphat

172 micellization were determined for dioctanoyl phosphatidylglycerol (PG) and phosphatidylserine (PS) at

173 ajor classes of phospholipids, we identified phosphatidylglycerol (PG) as the immunodominant lipid an

174 utant form of AmtB that abolishes a specific phosphatidylglycerol (PG) binding site, we observed dist

175 We previously showed that phosphatidylglycerol (PG) can regulate keratinocyte func

176 of the polar head group of the phospholipid phosphatidylglycerol (PG) catalyzed by Ala-tRNA(Ala)-dep

177 We found CL and phosphatidylglycerol (PG) concentrated in the polar regi

178 The negatively charged lipid phosphatidylglycerol (PG) constitutes up to 10% of total

179 ipid bilayer, certain bacteria add lysine to phosphatidylglycerol (PG) converting the net negative ch

180 We have previously found that phosphatidylglycerol (PG) derived from soy can inhibit i

181 In contrast, phosphatidylglycerol (PG) has a dominant inhibitory effe

182 n as well as the glycerol hydroxyl groups of phosphatidylglycerol (PG) has been investigated.

183 y be a result of the increased proportion of phosphatidylglycerol (PG) in fab1 that are high-melting-

184 transfer amino acids from aminoacyl-tRNAs to phosphatidylglycerol (PG) in the cytoplasmic membrane.

185 Phosphatidylglycerol (PG) is an important membrane polyg

186 choline (PC) lipids, which are zwitterionic; phosphatidylglycerol (PG) lipids, which are anionic; and

187 C) lipids alone or in admixture with anionic phosphatidylglycerol (PG) lipids.

188 Phosphatidylglycerol (PG) makes up 5-20% of the phosphol

189 In phosphatidylcholine (PC) and phosphatidylglycerol (PG) membranes, the TMD is predomin

190 dated, Here, we find a significant effect of phosphatidylglycerol (PG) on the folding of a trimeric a

191 In contrast, phosphatidylglycerol (PG) shows a strong and dominant in

192 ino acids from aminoacyl-tRNAs (aa-tRNAs) to phosphatidylglycerol (PG) to form aa-PG in the cytoplasm

193 Specific aminoacylation of the phospholipid phosphatidylglycerol (PG) with alanine (or with lysine)

194 consist mainly of phosphatidylethanolamine, phosphatidylglycerol (PG), and cardiolipin.

195 lipids sulfoquinovosyldiacylglycerol (SQDG), phosphatidylglycerol (PG), and glucuronosyldiacylglycero

196 a broad phospholipid spectrum, including PC, phosphatidylglycerol (PG), and phosphatidylinositol.

197 l (MGDG), digalactosyldiacylglycerol (DGDG), phosphatidylglycerol (PG), and sulfoquinovosyldiacylglyc

198 vestigate the effect of cardiolipin (CL) and phosphatidylglycerol (PG), anionic lipids important for

199 omprised of glycolipids and the phospholipid phosphatidylglycerol (PG), are essential for normal plan

200 lass of MprF can use Lys-tRNA(Lys) to modify phosphatidylglycerol (PG), but the mechanism of recognit

201 Here, we identified phosphatidylglycerol (PG), diphosphatidylglycerol (DPG,

202 by partial, outside-only exchange of anionic phosphatidylglycerol (PG), mimicking this key asymmetry

203 ids, monogalactosyldiacylglycerol (MGDG) and phosphatidylglycerol (PG), of the endosymbiont were sele

204 oethanolamine (PE), phosphatidylserine (PS), phosphatidylglycerol (PG), phosphatidylinositol (PI), an

205 stitution of BMP with its structural isomer, phosphatidylglycerol (PG), significantly reduced both le

206 tidylglycerol (1-acyllyso-PG), but not PE or phosphatidylglycerol (PG), to form a diacylated product

207 Delta, which lacks both CL and the precursor phosphatidylglycerol (PG), was significantly decreased a

208 e the physiological alcohol glycerol to form phosphatidylglycerol (PG), we hypothesized that AQP3 pro

209 nts also lack the immediate precursor to CL, phosphatidylglycerol (PG), when grown on glucose as a ca

210 The exception is phosphatidylglycerol (PG), which is an acidic/anionic ph

211 (1-->, occurs as a cyclic form (ECA(CYC)), a phosphatidylglycerol (PG)-linked form (ECA(PG)), and an

212 e anionic phospholipids cardiolipin (CL) and phosphatidylglycerol (PG).

213 t of giant unilamellar vesicles that contain phosphatidylglycerol (PG).

214 primarily phosphatidylethanolamine (PE) and phosphatidylglycerol (PG).

215 elates with the target membrane's content of phosphatidylglycerol (PG).

216 d mixtures: 1), phosphatidylcholine (PC) and phosphatidylglycerol (PG); 2), PC, PG, with 40 mol % cho

217 nsistent with variants of cardiolipins (CL), phosphatidylglycerols (PG), phosphatidylethanolamines (P

218 s, sulfoquinovosyldiacylglycerols (SQDG) and phosphatidylglycerols (PG).

219 e resolved from its structural isomer (i.e., phosphatidylglycerol, PG, another low-abundance class of

220 ds, amino acids and phosphatidic acid (PAs), phosphatidylglycerol (PGs), glycerophospholipids (PI), p

221 ics analysis identified associations between phosphatidylglycerols (PGs) and gut microbiota dysbiosis

222 onoacyl molecular species, galactolipids and phosphatidylglycerols (PGs) with oxidized fatty acyl cha

223 toyl-sn-glycero-3-phosphocholine (DMPC)) and phosphatidylglycerols (PGs, such as 1,2-dimyristoyl-sn-g

224 phosphatases catalyzing dephosphorylation of phosphatidylglycerol phosphate (PGP) to generate phospha

225 ephosphorylation of its immediate precursor, phosphatidylglycerol phosphate (PGP) whose synthase in E

226 ycerophospholipids like phosphatidic acid or phosphatidylglycerol phosphate are very poor substrates.

227 cently reported that PTPMT1 dephosphorylates phosphatidylglycerol phosphate, an essential intermediat

228 n Agrobacterium tumefaciens is selective for phosphatidylglycerol phosphate, demonstrating the import

229 ycerol 3-phosphate, generating the precursor phosphatidylglycerol-phosphate (PGP).

230 tive orthologs of Escherichia coli pgpB, the phosphatidylglycerol-phosphate phosphatase, from H. pylo

231 hat phosphatidylglycerol synthesized via the phosphatidylglycerol-phosphate synthase is not synthesiz

232 r the anionic phosphorylated lipids, such as phosphatidylglycerol, phosphatidic acid, and phosphatidy

233 lcholine, but addition of the anionic lipids phosphatidylglycerol, phosphatidic acid, or cardiolipin

234 amines, sphingomyelins, phosphatidylserines, phosphatidylglycerol, phosphatidic acids, ceramide phosp

235 consist mainly of phosphatidylethanolamine, phosphatidylglycerol, phosphatidylcholine, and two lipid

236 (6)f contains sulfoquinovosyldiacylglycerol, phosphatidylglycerol, phosphatidylcholine, monogalactosy

237 uents of Moraxella catarrhalis membranes are phosphatidylglycerol, phosphatidylethanolamine, and card

238 synthesized disaturated phosphatidylcholine, phosphatidylglycerol, phosphatidylethanolamine, and phos

239 sphatidylinositol dimannosides, cardiolipin, phosphatidylglycerol, phosphatidylethanolamine, trehalos

240 The method shows that fatty acids, phosphatidylglycerols, phosphatidylethanolamines, phosph

241 osphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylinositol, phosphatidyl

242 sphatidylethanolamines, phosphatidylserines, phosphatidylglycerols, phosphatidylinositols, phosphatid

243 ic phospholipids tested (phosphatidylserine, phosphatidylglycerol, phosphatidylmethanol, and cardioli

244 s stimulated by anionic lipids (cardiolipin, phosphatidylglycerol, phosphatidylserine, and CDP-diacyl

245 g phosphatidylcholine, phosphatidylinositol, phosphatidylglycerol, phosphatidylserine, diphosphatidyl

246 a are analyzed for phosphatidylethanolamine, phosphatidylglycerol, phosphatidylserine, phosphatidylin

247 els a small but biochemically active plastid phosphatidylglycerol pool in developing Arabidopsis embr

248 ine (POPC)/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylglycerol (POPG) (95/5, mol/mol) has been det

249 lmonary surfactant complex, palmitoyl-oleoyl-phosphatidylglycerol (POPG) and phosphatidylinositol (PI

250 tidylethanolamine (POPE) and palmitoyloleoyl-phosphatidylglycerol (POPG) lipids mimicking the inner m

251 nd anionic 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylglycerol (POPG) lipids.

252 ry surfactant phospholipid, palmitoyl-oleoyl-phosphatidylglycerol (POPG), antagonized the proinflamma

253 ine (POPC)/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylglycerol (POPG), as expected, with a tilt an

254 ry surfactant phospholipid, palmitoyl-oleoyl-phosphatidylglycerol (POPG), could markedly attenuate in

255 e anionic phospholipid, 1-palmitoyl-2-oleoyl phosphatidylglycerol (POPG), preferentially binds to and

256 AmtB specifically binds 1-palmitoyl-2-oleoyl phosphatidylglycerol (POPG).

257 ixture of 75% POPE, 20% 1-palmitoyl 2-oleoyl-phosphatidylglycerol (POPG); and 5% 1-palmitoyl 2-oleoyl

258 phate, necessary for the penultimate step in phosphatidylglycerol production, decreased by 58% in dia

259 First, phosphatidylglycerol:prolipoprotein diacylglyceryl trans

260 identify AmtB as being highly selective for phosphatidylglycerol, prompting us to obtain an X-ray st

261 Anionic phospholipids, like phosphatidylglycerol (PtdGro), were required for DgkB to

262 Inclusion of 3% pyrene-labeled phosphatidylglycerol (pyrene-PG) in the membrane reveale

263 wn ats1 mutants of near wild-type amounts of phosphatidylglycerol raised the question of whether an a

264 n of high-melting-point molecular species of phosphatidylglycerol relative to fab1.

265 of the Delta(3-trans) hexadecanoyl group in phosphatidylglycerol relative to wild type.

266 diolipin (CL), phosphatidylethanolamine, and phosphatidylglycerol remodeling cause Barth syndrome and

267 The biosynthesis of phosphatidylglycerol represents a central pathway in lip

268 Among other species, phosphatidylglycerol species were increased in normoxic

269 A molecular species of phosphatidylglycerol specific to chloroplasts of plants

270 parallel, the structure of the related lysyl-phosphatidylglycerol-specific L-PGS domain from Bacillus

271 catalyzed by Ala-tRNA(Ala)-dependent alanyl-phosphatidylglycerol synthase (A-PGS) or by Lys-tRNA(Lys

272 (A-PGS) or by Lys-tRNA(Lys)-dependent lysyl-phosphatidylglycerol synthase (L-PGS) enables bacteria t

273 Aminoacyl-phosphatidylglycerol synthases (aaPGSs) are membrane pro

274 under control of the ADH1 promoter restored phosphatidylglycerol synthesis and expression of mtGFP.

275 These studies also suggest that phosphatidylglycerol synthesized via the phosphatidylgly

276 The synthesis of tetrabutlyammonium phosphatidylglycerol (TBAPG), and a detailed spectral ch

277 yl groups from a unique chloroplast-specific phosphatidylglycerol that contains 16:1 (Delta3trans) as

278 In fab1 leaves, phosphatidylglycerol, the major chloroplast phospholipid

279 In fab1 leaves, phosphatidylglycerol, the major chloroplast phospholipid

280 increased with increasing concentrations of phosphatidylglycerol to 50 mol %.

281 ted MprF protein, which adds lysyl groups to phosphatidylglycerol to neutralize membrane surface char

282 inositol, -inositol-3- and -4-phosphate, and phosphatidylglycerol to phosphatidic acid (PA) in vitro.

283 the 2'-OH glycerol moiety on cardiolipin and phosphatidylglycerol to produce diacylglycerol (DAG), di

284 s lipids are synthesized consistently with a phosphatidylglycerol-to-sulfolipid and a phosphatidychol

285 of 3',6-dinonyl neamine with cardiolipin and phosphatidylglycerol, two negatively charged lipids from

286 deformation upon alpha-synuclein binding to phosphatidylglycerol vesicles at protein concentrations

287 scattering, we found that alphaS can remodel phosphatidylglycerol vesicles into nanoparticles whose s

288 The structure of Listeria phosphatidylglycerol was distinct from mammalian phospha

289 containing mutants, whereas the CL precursor phosphatidylglycerol was elevated.

290 was incubated with permeabilized HL60 cells, phosphatidylglycerol was released, and PA and PI were no

291 rome c to anionic lipid bilayers of dioleoyl phosphatidylglycerol was studied in low ionic strength p

292 Phosphatidylglycerol was the only surfactant lipid to si

293 e direct metabolic precursor of cardiolipin, phosphatidylglycerol, was also substantially depleted (2

294 s little as 10-15 mol % of an anionic lipid, phosphatidylglycerol, was present.

295 ylcholine, a phosphatidylethanolamine, and a phosphatidylglycerol were investigated.

296 Phosphatidylinositol, phosphatidylserine and phosphatidylglycerol were minor glycerophospholipids.

297 hosphatidylserine, phosphatidylinositol, and phosphatidylglycerol, were unable to facilitate recPrP(S

298 logically relevant D-stereoisomer of PS, and phosphatidylglycerol, which are not normally present in

299 nantly by saturated phosphatidylcholines and phosphatidylglycerols, which are major lipid components

300 s were markedly enriched for polyunsaturated phosphatidylglycerols with longer acyl chains, with step