ライフサイエンスコーパス: glycolipid

1 of the TA chain to either peptidoglycan or a glycolipid.

2 vivo by incorporating an NKT cell-activating glycolipid.

3 ily members that are specific for C1P versus glycolipid.

4 mechanism for recognizing this mycobacterial glycolipid.

5 ect the thermal hysteresis properties of the glycolipid.

6 he carbohydrate portion of glycoproteins and glycolipids.

7 ide (NO) upon challenge with corynebacterial glycolipids.

8 ssential enzyme involved in assembling these glycolipids.

9 membrane lipids are replaced with amino- or glycolipids.

10 of total non-starch lipids, or non-polar and glycolipids.

11 of globotrioasylceramide (GL-3) and related glycolipids.

12 key component of specific proteoglycans and glycolipids.

13 loid cells and sense mycobacterial cell wall glycolipids.

14 lated glycan structures on glycoproteins and glycolipids.

15 arbohydrate-carbohydrate interaction between glycolipids.

16 iling the temporal accumulation of different glycolipids.

17 characterized its binding to CD1d-presented glycolipids.

18 nd relative quantification of intact neutral glycolipids.

19 nd phospholipids at the interface along with glycolipids.

20 teraction of the M. leprae-specific phenolic glycolipid 1 (PGL-1) with myelinating glia and their sub

21 A glycolipid 3-sulfate group was essential for the T cell

22 T cell function by endogenous brain-derived glycolipids, a family of molecules traditionally deempha

23 for polymerizing the beta-Kdo linker on its glycolipid acceptor.

24 iency in which the ganglioside GM2 and other glycolipids accumulate intracellularly within lysosomes.

25 Alpha-gal-containing glycolipids activate basophils sensitized with plasma fr

26 However, it is unknown whether these glycolipids activate human innate immune cells through t

27 Moreover, glycolipid-activated iNKT cells increased the serum conc

28 r mechanism dominates in the face of cognate glycolipid activation during chronic inflammation, as mi

29 oreover, the cHA(mg) vaccine combined with a glycolipid adjuvant designed for class switch further en

30 augmented and or prolonged presentation of a glycolipid Ag leads to increased activation of NK cells

31 y, treating DR4tg mice with a TH2-polarizing glycolipid agonist of iNKT cells reduced SEB-inflicted m

32 marker PD1 and responded poorly to a strong glycolipid agonist.

33 lation characterized by their recognition of glycolipid Ags and rapid cytokine production upon activa

34 lls provide rapid innate T cell responses to glycolipid Ags from host cells and microbes.

35 ge of effector functions upon recognition of glycolipid Ags presented by CD1d.

36 espond to self and microbe-derived lipid and glycolipid Ags presented by the CD1d molecule.

37 T lymphocytes that recognize and respond to glycolipid Ags such as alpha-galactosylceramide (alpha-G

38 tion of Siglec-7 can be exploited to deliver glycolipid Ags to their target cell and increase the eff

39 iNKT cells to respond even in the absence of glycolipid Ags, for example, during viral infections.

40 Namely, the glycolipids alpha-glucosylceramide and isoglobotrihexosy

41 table for studying protein interactions with glycolipids, an important class of cellular receptors.

42 nt of sample needed, N-glycan, O-glycan, and glycolipid analyses are performed on the same enriched f

43 nd quantification strategy to advance intact glycolipids analysis in mammalian cells.

44 GPIHBP1 is a glycolipid-anchored membrane protein of capillary endoth

45 unoblotting, flow cytometry, and LC-MS-based glycolipid and glycan profiling, we found that CRISPR/Ca

46 eered sialic acids were detected in both the glycolipid and glycoprotein fractions of MLV producer ce

47 terial cord factor, is an abundant cell wall glycolipid and major virulence factor of Mycobacterium t

48 or imbalances in NSs and dramatic changes in glycolipids and glycoproteins, including a subset of int

49 thogens such as bacteria and viruses as both glycolipids and glycoproteins.

50 affect T cells that recognize mycobacterial glycolipids and influence immunity.

51 Like proteins, such as CD1D and MR1, present glycolipids and microbial riboflavin precursor derivativ

52 ith associated N-linked glycans and identify glycolipids and phospholipids in the V(o) complex.

53 al lipids, consisting of 72.8% punicic acid, glycolipids and phospholipids rich in essential fatty ac

54 ted, together with enhanced turnover of both glycolipids and phospholipids, supporting the drastic ne

55 are found on both N- and O-glycoproteins and glycolipids and play an important role in development, i

56 The glycolipids and the glycosylated V(o) subunits form a lu

57 Our data suggest that the four glycolipids and the nonphospholipid diacylglyceryl trime

58 Thylakoid membrane lipids, comprised of glycolipids and the phospholipid phosphatidylglycerol (P

59 e of several enzymes that controls levels of glycolipids and whose activity is linked to several huma

60 eins involved in the modification of surface glycolipids and, surprisingly, the auxiliary proteins of

61 AP domain are able to bind sterol and acidic glycolipid, and are involved in sterol transport and bet

62 LEC18 modulates host immunity via binding to glycolipids, and are also involved in glycolipid transpo

63 nd in block copolymers, surfactants, lipids, glycolipids, and other complex molecules.

64 Anti-glycolipid antibody activity was found in 13 (31%) patie

65 We stimulated iNKT cells by cognate glycolipid antigen alpha-galactosylceramide (alphaGalCer

66 ctivation of invariant NKT (iNKT) cells with glycolipid antigen drove immunosuppression.

67 s might increase antigen capture and enhance glycolipid antigen presentation in addition to the class

68 sed expression of CD1c, which is involved in glycolipid antigen presentation, and of the immune compl

69 thus providing far greater scope for diverse glycolipid antigen recognition.

70 em during the characterization of lipids and glycolipids antigen presentation.

71 ed Streptococcus pneumonia, known to express glycolipid antigens activating NKT cells, increased the

72 cells are innate-like T cells that recognize glycolipid antigens and play critical roles in regulatio

73 Our results suggest that glycolipid antigens derived from intestinal commensal ba

74 the sharply reduced levels of CD1d-presented glycolipid antigens in ConA-treated GF mice compared wit

75 ubpopulation of T lymphocytes that recognize glycolipid antigens in the context of CD1d-mediated anti

76 are a subset of T lymphocytes that recognize glycolipid antigens presented by the CD1d molecule (CD1d

77 Glycolipid antigens recognized by alphabeta T-cell recep

78 c enzymes and lipases that process lipid and glycolipid antigens, as well as a set of lipid transfer

79 turing and presenting a variety of different glycolipid antigens, including multiple forms of alpha-g

80 chains that show differential recognition of glycolipid antigens.

81 Diacetylene-containing glycolipids are a unique class of compounds that are abl

82 hydrate polymers, glycoproteins and membrane glycolipids are among candidates for this role, it is he

83 Although all glycolipids are bound by the T cell receptor of type I N

84 suggest that these microbial alpha-mannosyl glycolipids are capable of being recognized by both the

85 The biosynthesis of phospholipids and glycolipids are critical pathways for virtually all cell

86 Trehalose glycolipids are found in many bacteria in the suborder C

87 Protein interactions with glycolipids are implicated in diverse cellular processes

88 ng simple mono- and disaccharides that mimic glycolipids are known to self-assemble into glycodendrim

89 Glycolipids are potent activator of natural killer T (NK

90 Due to their charge and ability to coalesce, glycolipids are therefore the likely primary EF sensor d

91 -to-analyze structures (e.g., proteoglycans, glycolipids), are functionally important in a biological

92 at PSV could recognize alpha2,3-linked SA on glycolipids as a receptor.

93 y approach that utilizes essential microbial glycolipids as chemical fingerprints for identification

94 n alpha-Gal allergic patients and identifies glycolipids as potential allergenic molecules.

95 aride molecules represent a unique family of glycolipids based on a highly conserved lipid moiety kno

96 n the synthesis and biological properties of glycolipids based on glucose and trehalose scaffolds whi

97 light on iNKT cells' mechanism of action and glycolipid-based immunotherapies.

98 responsible for synthesis of this conserved glycolipid belong to a new family of glycosyltransferase

99 ence of lipid bilayer composition on protein-glycolipid binding in vitro.

100 cific and has few cationic residues near its glycolipid binding site.

101 Rhamnolipids are amphiphilic glycolipids biosynthesized by bacteria that, due to thei

102 only increased the ionization efficiency of glycolipids but also facilitated structural characteriza

103 probes, we studied the mobilities of labeled glycolipids by time-lapse microscopy and fluorescence re

104 n the thymus, precursor cells recognize self-glycolipids by virtue of their semi-invariant TCR, which

105 us homologous series of l-ascarylose-derived glycolipids called ascarosides, which include several hi

106 Unique glycolipids called lipopolysaccharide/lipooligosaccharid

107 all arabinan, demonstrating that non-natural glycolipids can serve as biosynthetic intermediates and

108 Alkyl glycosides, glycolipids, can bind to both S1 and a second site, S2.

109 typal CDC requires interaction with the sLeX glycolipid cellular receptor as an essential step before

110 he enzymes that build the conserved terminal glycolipid characterizing other capsules using this meth

111 to which the relative abundances of protein-glycolipid complexes observed by ESI-MS reflect the rela

112 However, the study of protein-glycolipid complexes remains a significant experimental

113 e the backbone of a novel thermal hysteresis glycolipid containing a linear glycan sequence of altern

114 for iNKT cells has led to the development of glycolipid containing nanoparticles which efficiently ac

115 The potentially antigenic alpha-mannosyl glycolipids contributed to the protection of mice agains

116 raits of Pi starvation, such as phospholipid/glycolipid conversion, and the accumulation of starch an

117 Here, we test the role of glycolipid crosslinking as a raft targeting and ordering

118 nd O-glycans from pig lung glycoproteins and glycolipid-derived glycans were fluorescently tagged and

119 urther, activation of iNKT cells via cognate glycolipid during IL-18-mediated inflammation overrides

120 The glycolipids enhanced expression of a subset of IFN-gamma

121 fatides and gangliosides are raft-associated glycolipids essential for maintaining myelinated nerve i

122 antigen, including binding analyses with the glycolipid extract of the prostate cancer cell line PC3,

123 Here, we show that glycolipid extracts from the cell walls of several patho

124 e bartolosides, unprecedented cyanobacterial glycolipids featuring aliphatic chains with chlorine sub

125 actions with adhesion receptors and sulfated glycolipids (Figure 1, bottom).

126 Depletion of cell surface glycolipids followed by reconstitution studies indicated

127 represent an attractive method to solubilize glycolipids for protein interaction studies in aqueous s

128 with PE from M. smegmatis may offer clues to glycolipid formation in M. tuberculosis.

129 The Lipid A family of glycolipids, found in the outer membranes of all Gram-ne

130 is of a complex beta-1,2-mannosyloxymannitol glycolipid from Malassezia pachydermatis 44-2, which was

131 y leads to the accumulation of the cytotoxic glycolipid, galactosylsphingosine (psychosine).

132 The cell membrane glycolipid GD2 is expressed by multiple solid tumors, in

133 in A and lipids, PDs), to screen mixtures of glycolipids (GLs) against water-soluble proteins to dete

134 ith the use of nanodiscs (NDs) to solubilize glycolipids (GLs) has recently emerged as a promising an

135 -1 (GCase) catalyzes the cleavage of a major glycolipid glucosylceramide into glucose and ceramide.

136 The glycocalyx is a thin layer of glycolipids, glycoproteins, and proteoglycans on the sur

137 pha-1,3-galactose) ubiquitously expressed on glycolipids/glycoproteins of most mammals.

138 njugates (glycosaminoglycans, glycoproteins, glycolipids, glycosylphosphatidylinositol-anchored prote

139 The influence of the glycolipid GM1 on the physical properties of POPC membra

140 The ganglioside (glycolipid) GM1 is thought to be the sole CT receptor; h

141 seven different lipids species including the glycolipid GM3 in the outer leaflet and the anionic lipi

142 ed form of GIFT4 was constructed by fusing a glycolipid (GPI)-anchoring sequence and incorporated int

143 Lipoarabinomannan (LAM), a surface glycolipid, has been identified as a potential TB biomar

144 While a growing number of bacterial glycolipids have been discovered that can signal through

145 Several unique mycomembrane glycolipids have been isolated and structurally characte

146 Heterocyst glycolipids (HGs) provide an extracellular gas diffusion

147 eral blood samples, along with anti-phenolic glycolipid I serology and skin tests from the same indiv

148 18.3% (19 of 104 samples) for anti-phenolic glycolipid I serology.

149 The antigenic glycolipids identified to date consist of two hydrophobi

150 n IgE-dependent manner suggesting a role for glycolipid in the effector phase of IgE-mediated food al

151 a small number of phospholipids, to display glycolipids in a lipid environment for protein-glycolipi

152 resent evidence that hopanoids interact with glycolipids in bacterial outer membranes to form a highl

153 was <6% measured across four representative glycolipids in five different ratios and triplicate expe

154 Probing the role of glycolipids in health and disease warrants development o

155 ore conjugates capable of labeling trehalose glycolipids in live actinomycetes.

156 p between NKT cells and intestinal bacterial glycolipids in liver disorders remained unclear.

157 ccharides (LPS) are essential outer membrane glycolipids in most gram-negative bacteria.

158 ng the distribution of numerous phospho- and glycolipids in mouse cerebellum and kidney slices, and i

159 Glycolipids in Mycobacterium tuberculosis, the causative

160 titative studies of lectin interactions with glycolipids in native-like, membrane environments.

161 -glycans of glycoproteins, as well as intact glycolipids in parallel, using the same enriched membran

162 induce antibodies that cross-react with self-glycolipids in peripheral nerves, causing neuropathy.

163 cinal potential of the ipomoeassin family of glycolipids in the future.

164 , which are required for the biosynthesis of glycolipids in the plastids.

165 sses of biomolecules, including phospho- and glycolipids in tissue sections at high lateral resolutio

166 When analyzing the low abundant glycolipids in total lipid extract, permethylation can d

167 nd chemical modifications (including various glycolipids) in the PDB, and both PDB and PDBx/mmCIF for

168 Several microbial alpha-mannosyl glycolipids, in which the 2'-OH group is in the trans or

169 Furthermore, these glycolipids induced the production of proinflammatory cy

170 the adaptor protein CARD9 were essential for glycolipid-induced IL-8 production.

171 CT glycolipid infiltration was defined as focal, moderate,

172 ate bacteria-bilayer interactions by probing glycolipids inside the model membrane scaffold.

173 ycolipids in a lipid environment for protein-glycolipid interaction studies in aqueous solution.

174 of low, moderate, and high affinity protein-glycolipid interactions serve to demonstrate the reliabi

175 These high-resolution views of how a glycolipid interacts with an antibody may help to advanc

176 g to the regions where the respective target glycolipid is specifically localised.

177 Profiling of the glycans and the glycolipids is performed using nanoflow liquid chromatog

178 carbon (PGC) column, while the N-glycans and glycolipids isolated from the same cell membrane fractio

179 s of F. thermalis constitutively overproduce glycolipid isomers associated with high temperature to l

180 ral killer T (NKT) -cells activated with the glycolipid ligand alpha-galactosylceramide (alpha-GalCer

181 ith alpha-galactosylceramide, the prototypic glycolipid ligand of iNKT cells, result in anergy.

182 bunits and identifying a novel and conserved glycolipid ligand.

183 dated, but the basis for enhanced binding to glycolipid ligands, in which hydrophobic substituents ar

184 he cerebellum, and secondary accumulation of glycolipids like GM2 and GM3 gangliosides and unesterifi

185 vaccine incorporating an NKT cell-activating glycolipid linked to an MHC class I-restricted peptide f

186 glycerides affected transfer action by human glycolipid lipid transfer protein (GLTP), which is glyco

187 -TOF mass spectrometry of bacterial membrane glycolipids (lipid A) has the potential to identify micr

188 d by concentrating the tuberculosis-specific glycolipid, lipoarabinomannan (LAM), a promising urinary

189 Mycobacterium tuberculosis cell wall glycolipid, lipoarabinomannan, can inhibit CD4(+) T cell

190 mannan, and lipoarabinomannan, which are key glycolipids/lipoglycans of the mycobacterial cell envelo

191 two cellular membranes, with the specialized glycolipid lipopolysaccharide (LPS) exclusively found on

192 olipids in the inner leaflet and the complex glycolipid lipopolysaccharide (LPS) in the outer leaflet

193 can (wall teichoic acid, WTA) or to membrane glycolipids (lipoteichoic acid, LTA).

194 an (wall teichoic acids; WTA) or to membrane glycolipids (lipoteichoic acids; LTA).

195 GM2/GD2 gangliosides are surface glycolipids mainly found on brain neurons as well as per

196 1 was originally proposed to translocate the glycolipid Man5GlcNAc2-PP-dolichol (needed to synthesize

197 A library of glycolipid mass spectra from 50 microbial entries was de

198 These results demonstrate that bacterial glycolipid mass spectra represent chemical barcodes that

199 s (e.g., dot products) do not work well with glycolipid mass spectra such as those produced by lipid

200 MALDI-TOF-MS in negative ion mode to obtain glycolipid mass spectra.

201 As the diversity in our glycolipid mass spectral library increases, we anticipat

202 Our results indicate that glycolipid-mediated membrane adhesion is a highly abunda

203 monodisperse oligomers containing lipid and glycolipid mimics.

204 mportant implications for the application of glycolipid molecules as vaccine adjuvants.

205 otent biological activities of these complex glycolipid natural products.

206 ntigen (ECA), a non-essential outer membrane glycolipid of the Enterobacteriaceae.

207 Outer membrane (OM)-associated glycolipids of gut commensal microbes belonging to the B

208 Glycoproteins and glycolipids of some mammalian species contain the disacc

209 can induce aggregation with glycoproteins or glycolipids on the cell surface and thereby regulate cel

210 Here, the influence of various glycolipids on the interaction between adjacent membrane

211 lycans that are carried as glycoproteins and glycolipids on the outer leaflets of their plasma membra

212 stal structures of 19 different binary (CD1d-glycolipid) or ternary (CD1d-glycolipid-TCR) complexes a

213 ometric data as well as plasma Hcy level and glycolipid parameters were collected.

214 1-ganglioside bridges arising from preformed glycolipid patches cross-link the complexes.

215 Here we examine the effect of a glycolipid-peptide conjugate vaccine incorporating an NK

216 Glycolipid-peptide conjugate vaccines may prove useful f

217 cal role for mycobacterial membrane phenolic glycolipid (PGL) in engineering this transition.

218 veal in vivo functions for specific phenolic glycolipids (PGLs) in the mycobacteria that cause tuberc

219 n clinical laboratories, a reliable MS-based glycolipid phenotyping method that identifies colistin r

220 y components of the cell wall, including the glycolipids phosphatidylinositol mannoside, lipomannan,

221 Gangliosides (sialylated glycolipids) play an essential role in the CNS by regula

222 ) are high-molecular-weight, surface-exposed glycolipids present in a broad range of nontuberculous m

223 e a unique lineage of T cells that recognize glycolipid presented by CD1d.

224 e and innate lymphocytes, and they recognize glycolipids presented by an MHC class I-like CD1d molecu

225 Some synthetic and bacterial glycolipids presented by CD1d specifically activate inva

226 cells are innate lymphocytes that respond to glycolipids presented by the MHC class Ib molecule CD1d

227 e-like lymphocyte population that recognizes glycolipids presented on CD1d.

228 e thymus and periphery due to defective self glycolipid processing and presentation by DP thymocytes

229 common basic structure with trehalose-based glycolipids produced by Mycobacterium tuberculosis TPP p

230 Because the molecular mechanisms of glycolipid production are conserved among mycobacteria,

231 Additionally, glycolipid profiling was able to differentiate A. bauman

232 n glycans (sugars) existing predominantly as glycolipids, proteoglycans, or glycoproteins formed by t

233 Glycolipid-reactive T cells expressed memory markers and

234 HIV infection, and tracked the mycobacterial glycolipid-reactive T-cell repertoire by using CD1b tetr

235 It has been shown that CD1d expression and glycolipid-reactive, CD1d-restricted NKT cells exacerbat

236 Anti-glycolipid reactivity was studied in patients with Guill

237 binds the sialic acid moiety of glycoprotein/glycolipid receptors on host cells.

238 n mimics inhibited IAV binding to underlying glycolipid receptors, and this density correlated to the

239 e gained insight into the molecular bases of glycolipid recognition by Mincle.

240 NKT cells represent a small subset of glycolipid-recognizing T cells that are heavily implicat

241 e glycoproteins following N-glycan and lipid/glycolipid removal by PNGase F digestion and Folch extra

242 Unconventional, glycolipid-responsive T cells contributed to reduced myc

243 link clinical and mechanistic evidence that glycolipid-responsive, polycytotoxic T cells contribute

244 obacteria, nocardia, and rhodococci) share a glycolipid-rich cell wall dominated by mycolic acids (te

245 sistant membranes, which contain cholesterol-glycolipid-rich membrane regions known as lipid rafts, s

246 Mycobacteria have a distinctive glycolipid-rich outer membrane, the mycomembrane, which

247 hese data indicate that, in addition to self-glycolipids, self-lysophospholipids are also recognized

248 k areas between the (12)C- and (13)C-labeled glycolipids served as surrogate measure of their relativ

249 ipid lipid transfer protein (GLTP), which is glycolipid-specific and has few cationic residues near i

250 Invariant natural killer T (iNKT) cells (glycolipid-specific, CD1d-restricted innate lymphocytes)

251 l protein-deficient mice suggests that these glycolipids stabilize membrane proteins including neurof

252 ase activity and protein levels, and reduced glycolipid storage in both iPSC-derived macrophages and

253 dase activity and protein levels and reduced glycolipid storage.

254 asurements of enzyme catalyzed hydrolysis of glycolipid substrates and the detection of low, moderate

255 d glucocerebrosidase activity and stored the glycolipid substrates glucosylceramide and glucosylsphin

256 eptive neurons in vitro and identify the Mtb glycolipid sulfolipid-1 (SL-1) as the nociceptive molecu

257 e in co-ordination with cell division, while glycolipid synthesis takes place throughout the membrane

258 Another iminosugar activity, inhibition of glycolipid synthesis, resulted in a drug for Gaucher dis

259 it is able to increase overall phospho- and glycolipid synthesis.

260 fic embryonic antigen-4 (SSEA-4) is one such glycolipid target expressed in many cancers, including b

261 nt binary (CD1d-glycolipid) or ternary (CD1d-glycolipid-TCR) complexes at resolutions between 1.67 an

262 ticularly enriched in sialic acid-containing glycolipids termed gangliosides.

263 nt Gram-negative pathogens share a conserved glycolipid terminus containing 3-deoxy-beta-d- manno-oct

264 Glycosylphosphatidylinositol (GPI) is a glycolipid that anchors >150 various proteins to the cel

265 vironment and process it to form cholesterol glycolipids that are incorporated onto their membranes.

266 alactan layer or incorporated into trehalose glycolipids that associate with the MM non-covalently.

267 Polymerizable diacetylene glycolipids that can function as low molecular weight ge

268 Glycosphingolipids are a subgroup of glycolipids that contain an amino alcohol sphingoid base

269 arides, glycoproteins, and proteoglycans, to glycolipids that make up a complex glycan code that impa

270 acid terminates glycans of glycoproteins and glycolipids that play numerous biological roles in healt

271 re we show that ascaroside pheromones, small glycolipids that signal population density, suppress exp

272 n done to identify the structures of natural glycolipids that stimulate NKT cells and to determine ho

273 bolism intermediates instead of cell surface glycolipids, thus maintaining levels of ATP and antioxid

274 found to play a key role in the binding of a glycolipid to the carbohydrate recognition domain of the

275 ical MHC molecule able to present lipids and glycolipids to a specialized subset of T cells known as

276 ydrophilic lipooligosaccharides and phenolic glycolipids to hydrophobic phthiocerol dimycocerosates,

277 hesis, assembly, and export of these complex glycolipids to the cell surface are the object of the pr

278 d nearly ubiquitous two-layer, alpha-helical glycolipid transfer protein (GLTP)-fold now further adva

279 TmrAB, and imply a role for this exporter in glycolipid translocation.

280 ing to glycolipids, and are also involved in glycolipid transportation and protein aggregation in the

281 Surprisingly, C. albicans-infected, glycolipid-treated mice exhibited significantly lower su

282 In the C. albicans-infected, glycolipid-treated mice, the number of neutrophils in th

283 usly shown that transient acetylation of the glycolipid trehalose monohydroxycorynomycolate (hTMCM) e

284 w route to access original glycopeptide- and glycolipid-type analogues possessing a C-C bond at the C

285 Phosphatidyl-inositol mannosides (PIM) are glycolipids unique to mycobacteria and other related bac

286 g chronic inflammation, as might result from glycolipid vaccination or infection during chronic autoi

287 so review studies designed to understand how glycolipid variants, both natural and synthetic, can alt

288 amers to isolate clones recognizing the same glycolipid, we identified a previously unknown pattern o

289 Gram-positive and negative bacterial glycolipids were extracted using a single optimized prot

290 Phospholipids and glycolipids were identified and quantified by LC-MS and

291 Both amphiphilic and dipolar glycolipids were synthesized, and these compounds are ef

292 ly, we found the intestinal bacteria contain glycolipids which can be presented by CD1d and recognize

293 Thus, our data demonstrate that glycolipids which engage iNKT cells support antigen-spec

294 This large glycolipid, which contains numerous sugars, is made in t

295 large family of glycans of glycoproteins and glycolipids whose branching and peripheral substitutions

296 Glycolipids with alpha-linked anomeric carbohydrates hav

297 atides and complex gangliosides are membrane glycolipids with important roles in maintaining nervous

298 produced in aquaponics have higher levels of glycolipids with n-3 fatty acids (DGDG 36:3; SQDG 36:3;

299 hts into the presentation and recognition of glycolipids with polar moieties in an otherwise apolar m

300 the underlying organization and dynamics of glycolipids within the cell envelope remain poorly under