ライフサイエンスコーパス: phosphatidylglycerol

1 eoyl phosphatidylglycerol; DMPG, dimyristoyl phosphatidylglycerol).

2 sphatidylethanolamine, phosphatidylserine or phosphatidylglycerol.

3 r by phosphate-masked phosphatidylcholine or phosphatidylglycerol.

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

5 om Escherichia coli is preloaded with PA and phosphatidylglycerol.

6 lipids of the cytoplasmic membrane, such as phosphatidylglycerol.

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

8 the nonreducing end following initiation on phosphatidylglycerol.

9 membranes contained phosphatidylcholine and phosphatidylglycerol.

10 alpha-synuclein is clustered are enriched in phosphatidylglycerol.

11 ructure in the micelles of SDS or dioctanoyl phosphatidylglycerol.

12 but did not decrease the relative amount of phosphatidylglycerol.

13 ipin-deficient mutant were characteristic of phosphatidylglycerol.

14 in demonstrated the presence of glycosylated phosphatidylglycerol.

15 tween the peptide and short chain dioctanoyl phosphatidylglycerol.

16 otropic phase in anionic bilayers containing phosphatidylglycerol.

17 rol to phospholipase D2 for the synthesis of phosphatidylglycerol.

18 nsion and identified them as cardiolipin and phosphatidylglycerol.

19 olipids in the presence of glycerol to yield phosphatidylglycerol.

20 ther peptides was not strongly influenced by phosphatidylglycerol.

21 phatidylethanolamine to 1-palmitoyl-2-oleoyl-phosphatidylglycerol.

22 hatidylethanolamine, phosphatidylserine, and 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 chain composition of phosphatidylcholine and phosphatidylglycerol.

28 rms oligomeric pores on membranes containing phosphatidylglycerol.

29 which occurs by binding surface disaturated phosphatidylglycerols.

30 mass spectrometry are a group of disaturated phosphatidylglycerols.

31 yl chain saturation of phosphatidic acid and phosphatidylglycerol, 2) large increases in the levels o

32 cerol or a mixture of anionic E. coli lipids phosphatidylglycerol (25%) and phosphatidylethanolamine

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

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

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

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

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

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

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

40 Synthetic cardiolipin or phosphatidylglycerol also induced pulmonary hypertension

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

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

43 hatidylethanolamine, diphosphatidylglycerol, phosphatidylglycerol and an unidentified aminophospholip

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

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

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

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

48 g concentration of the anionic phospholipids phosphatidylglycerol and cardiolipin.

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

50 s1Delta) of Saccharomyces cerevisiae lacking phosphatidylglycerol and cardiolipin.

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

52 pe under nonactivating conditions, i.e. with phosphatidylglycerol and in the absence of Ca(2+), indic

53 ne lipids sulfoquinovosyl diacylglycerol and phosphatidylglycerol and into a nonchloroplastic lipid p

54 phatidylcholine vesicles with anionic lipids phosphatidylglycerol and phosphatidic acid.

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

56 Liposomes composed of phosphatidylglycerol and phosphatidylcholine were monodi

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

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

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

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

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

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

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

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

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

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

67 ass of binding sites for phosphatidylserine, phosphatidylglycerol, and cardiolipin on TbMscL; binding

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

69 imyristoyl phosphatidyl choline, dimyristoyl phosphatidylglycerol, and cholesterol in a 4:1:4 molar r

70 (dihexanoyl phosphatidylglycerol, dioctanoyl phosphatidylglycerol, and didecanoyl phosphatidylglycero

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

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

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

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

75 es composed of mixtures of the acidic lipid, phosphatidylglycerol, and the neutral lipid, phosphatidy

76 aturated pulmonary surfactant phospholipids; phosphatidylglycerols, and phosphatidylcholines.

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

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

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

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

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

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

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

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

85 Phosphatidylglycerol, as a bioactive lipid, could potent

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

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

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

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

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

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

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

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

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

95 composed of monogalactosyldiacylglycerol and phosphatidylglycerol (both enriched with unsaturated fat

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

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

98 anolamine (C6PE), phosphatidylserine (C6PS), phosphatidylglycerol (C6PG), and an unnatural phospholip

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

100 various combinations of phosphatidylcholine, phosphatidylglycerol, cardiolipin, and cholesterol showe

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

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

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

104 eparations consisting of phosphatidylcholine/phosphatidylglycerol/cholesterol in various ratios and r

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

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

107 activities in conjunction with a decrease in phosphatidylglycerol content.

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 -sn-glycero-3-phosphocholine/1, 2-dielaidoyl-phosphatidylglycerol (DEPC/DEPG) liposomes at pH 5.0 as

111 osphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, digalactosyldiacylglycerol, monoga

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

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

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

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 l phosphatidylcholine (DPPC) and dipalmitoyl phosphatidylglycerol (DPPG) (9:1, mol:mol); and DPPC alo

119 nteraction with 1,2-dipalmitoyl-sn-glycero-3-phosphatidylglycerol (DPPG) liposomes.

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

121 hosphatidylinositol, phosphatidylserine, and phosphatidylglycerol, even when normalized for charge.

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

123 ly charged lipids like phosphatidylserine or phosphatidylglycerol for activity.

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

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

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

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

128 Intact polar lipids with phosphatidylglycerol headgroups and glycerol dibiphytany

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

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

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

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

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

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

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

136 in synthase activity is unchanged, saturated phosphatidylglycerol is a poor substrate for this enzyme

137 Phosphatidylglycerol is elevated in crd1 Delta mutant ce

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

139 um current (I(max)) at 25-30 mol% (dioleoyl)-phosphatidylglycerol ([L-]max) corresponding to a surfac

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

141 Remarkably, phosphatidylglycerol levels decreased with increasing ph

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

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

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

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

146 bundance of diglycerides, triglycerides, and phosphatidylglycerol lipids.

147 3 NS4B was reconstituted into lyso-myristoyl phosphatidylglycerol (LMPG) micelles.

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

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

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

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

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

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

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 in the presence of either the anionic lipid phosphatidylglycerol or a mixture of anionic E. coli lip

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

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

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

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

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

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

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

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

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

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

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

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

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

173 Phosphatidylglycerol (PG) and phosphatidylinositol (PI)

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

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

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

177 ine (PC), phosphatidylethanolamine (PE), and phosphatidylglycerol (PG) but induced an increase in pho

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

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

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

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

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

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

184 itical roles with which CL and its precursor phosphatidylglycerol (PG) have been associated.

185 AG-tagged Isc1p was activated by PS, CL, and phosphatidylglycerol (PG) in a dose-dependent manner.

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

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

188 Phosphatidylglycerol (PG) is an important membrane polyg

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

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

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

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

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

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

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

196 Mutant membranes have increased phosphatidylglycerol (PG) when grown in a nonfermentable

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

198 esicles made of phosphatidylcholine (PC) and phosphatidylglycerol (PG) with the following acyl-chain

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

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

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

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

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

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

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

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

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

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

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

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

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

212 (1-->, occurs as a cyclic form (ECA(CYC)), a phosphatidylglycerol (PG)-linked form (ECA(PG)), and an

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

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

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

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

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

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

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

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

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

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 osphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylserine, phosphatidylin

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

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

250 ibrate across phosphatidylcholine (POPC) and phosphatidylglycerol (POPG) bilayers, while four amphipa

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

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

253 ne (POPC) vesicles and -8.2 kcal mol(-1) for phosphatidylglycerol (POPG) vesicles.

254 E:cholesterol, 3:1 POPC:1-palmitoyl-2-oleoyl-phosphatidylglycerol (POPG), and 3:1 POPE:POPG were also

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

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

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

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

259 ethanolamine and cholesterol as well as with phosphatidylglycerol (previously reported).

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

261 First, phosphatidylglycerol:prolipoprotein diacylglyceryl trans

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

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

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

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

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

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

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

269 The biosynthesis of phosphatidylglycerol represents a central pathway in lip

270 The results suggest that phosphatidylglycerol saturation and subsequent decreases

271 Among other species, phosphatidylglycerol species were increased in normoxic

272 A molecular species of phosphatidylglycerol specific to chloroplasts of plants

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

274 Along with phosphatidylglycerol, sulfolipid contributes to maintain

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

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

277 Aminoacyl-phosphatidylglycerol synthases (aaPGSs) are membrane pro

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

279 These studies also suggest that phosphatidylglycerol synthesized via the phosphatidylgly

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

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

282 In fab1 leaves, phosphatidylglycerol, the major chloroplast phospholipid

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

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

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

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

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

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

289 The structure of Listeria phosphatidylglycerol was distinct from mammalian phospha

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

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

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

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 yristoyl phosphatidylcholine and dimyristoyl phosphatidylglycerol), with and without lanthanide ions