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 n that is retained within the membrane via a glycolipid.

4 related to the receptor and the role of this glycolipid.

5 ily members that are specific for C1P versus glycolipid.

6 mechanism for recognizing this mycobacterial glycolipid.

7 membrane lipids are replaced with amino- or glycolipids.

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

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

10 throughput annotations of previously unknown glycolipids.

11 ing the superior antitumor potency of phenyl-glycolipids.

12 2-fold higher than those treated with phenyl-glycolipids.

13 ccharides, glycoproteins, glycopeptides, and glycolipids.

14 s had no A antigens but instead expressed Fs glycolipids.

15 hydrate antigen, HNK-1, in glycoproteins and glycolipids.

16 ycerolipids, bacterial lipoglycans and plant glycolipids.

17 ria are known to produce polysaccharides and glycolipids.

18 ide (NO) upon challenge with corynebacterial glycolipids.

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

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

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

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

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

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

25 In this study, we demonstrate that glycolipid-activated iNKT cells cooperate with myeloid-d

26 Our data suggest that the glycolipid adjuvant TDB triggers Mincle-dependent IL-1 p

27 hat are coadministered with the CD1d-binding glycolipid Ag alpha-galactosylceramide (alpha-GC).

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

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

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

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

32 re a unique subset of T cells that recognize glycolipid Ags presented in the context of CD1d molecule

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

34 Activation of iNKT cells with glycolipid Ags, such as the marine sponge-derived reagen

35 ion, including exogenous NKT cell activator, glycolipid alpha-GalCer, and endogenous prostaglandin E2

36 Namely, the glycolipids alpha-glucosylceramide and isoglobotrihexosy

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

38 Glycolipid analysis confirmed a complete lack of GM3 gan

39 st glycerolphosphate (GroP) subunit onto the glycolipid anchor and the LTA synthase LtaS(Lm) extends

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

41 A mixture of two lipid species, a glycolipid and a phospholipid, with known affinities for

42 ehalose 6,6'-dimycolate (TDM) is a cell wall glycolipid and an important virulence factor of mycobact

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

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

45 tides constitute a major component of myelin glycolipids and are known to be capable of raising an im

46 is present in large numbers on cell membrane glycolipids and glycoproteins.

47 of viral glycoproteins or other host-derived glycolipids and glycoproteins.

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

49 ides (GlcAGroAc2) are functionally important glycolipids and membrane anchors for cell wall lipoglyca

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

51 which exploits nanodiscs (NDs) to solubilize glycolipids and mimic their natural cellular environment

52 une regulatory T cells with Ag reactivity to glycolipids and peptides, respectively.

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

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

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

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

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

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

59 interactions with nanodisc-embedded lipids, glycolipids, and membrane proteins.

60 cted examples of novel biobased surfactants, glycolipids, and polymers derived from cardanol, and the

61 rafts are ordered assemblies of cholesterol, glycolipids, and proteins that modulate proinflammatory

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

63 or priming iNKT cells in mice immunized with glycolipid antigen in particulate form.

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

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

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

67 y depending on the structure of a particular glycolipid antigen.

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

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

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

71 et of innate-like lymphocytes that recognize glycolipid antigens bound by the major histocompatibilit

72 tective immune response triggered by foreign glycolipid antigens bound to CD1d on antigen-presenting

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 which cells are the principal presenters of glycolipid antigens in vivo remains controversial, and i

77 Glycolipid antigens recognized by alphabeta T-cell recep

78 s express CD1d and are capable of presenting glycolipid antigens to invariant natural killer T cells

79 A limitation of using glycolipid antigens to stimulate immune responses in hum

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

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

82 chains that show differential recognition of glycolipid antigens.

83 alciparum apicoplasts, suggesting that these glycolipids are a hallmark of photosynthetic plastids an

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

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

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

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

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

89 Protein interactions with glycolipids are implicated in diverse cellular processes

90 Glycolipids are mainly found in phototrophic organisms (

91 cerol and glucuronosyl diacylglycerol or all glycolipids are not impaired in growth or virulence duri

92 Glycolipids are potent activator of natural killer T (NK

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

94 However, alpha-anomeric glycolipids are thought to be absent in mammals.

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

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

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

98 tions for the development of NKT-stimulatory glycolipids as vaccine adjuvants and anticancer therapeu

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

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

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

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

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

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

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

106 material (CRM) 197 (DT), and combined with a glycolipid C34 as an adjuvant designed to induce a class

107 n average (DT-RM4.7) and adjuvanted with the glycolipid C34, the combination exhibited the strongest

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

109 Unique glycolipids called lipopolysaccharide/lipooligosaccharid

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

111 osaccharides (LOSs) are cell surface-exposed glycolipids capable of modulating the host immune system

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

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

114 ycolipid antibodies that bind to heteromeric glycolipid complexes has generated new insights in this

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

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

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

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

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

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

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

122 re sialylated N-glycans but not O-glycans or glycolipid-derived glycans, and each virus demonstrated

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

124 ract of infants, and studies have shown that glycolipids extracted from the cell surface of these bac

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

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

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

128 Depletion of cell surface glycolipids followed by reconstitution studies indicated

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

130 omycoketide (C32-MPM), a naturally occurring glycolipid found in the cell walls of Mycobacterium tube

131 Asperamide B is thus the first fungal glycolipid found to directly activate iNKT cells.

132 f sufficient quantities of carbohydrates and glycolipids from biological samples remains a significan

133 ification and structural characterization of glycolipids from the cell wall of bifidobacteria is the

134 forms of Shiga toxin, Stx1 and Stx2, use the glycolipid globotriaosylceramide (Gb3) as their cellular

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

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

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

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 trafficking of individual glycoproteins and glycolipids has been noted in NPC cells and other storag

144 SSEA-4, a sialyl-glycolipid, has been commonly used as a pluripotent huma

145 Several unique mycomembrane glycolipids have been isolated and structurally characte

146 The other two glycolipids have now been identified by mass spectrometr

147 een developed in order to obtain constituent glycolipids, having multivalent sugar moieties and their

148 The cationic glycolipids here presented can be considered as new lead

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

150 18.3% (19 of 104 samples) for anti-phenolic glycolipid I serology.

151 The antigenic glycolipids identified to date consist of two hydrophobi

152 T cell activation across diverse settings of glycolipid immunization and systemic infection with Stre

153 Globo-H ceramide (GHCer), the most prevalent glycolipid in a majority of epithelial cancers and one t

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

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

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

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

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

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

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

161 xin (CT), enter the cell by first binding to glycolipids in the cell membrane.

162 ir target cells by first binding to specific glycolipids in the cell membrane.

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

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

167 Furthermore, these glycolipids induced the production of proinflammatory cy

168 Glycolipid-induced exacerbation of C. albicans infection

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

170 CT glycolipid infiltration was defined as focal, moderate,

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

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

173 f the assay for identifying specific protein-glycolipid interactions from biologically relevant mixtu

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

175 micelles include: (i) insertion of synthetic glycolipids into matrix lipids; (ii) preparation of glyc

176 our results suggest that R-LPS or a similar glycolipid is a physiological substrate of MacAB-TolC.

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

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

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

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

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

182 The glycolipid lipoarabinomannan (LAM) plays an important ro

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

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

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

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

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

188 1 was originally proposed to translocate the glycolipid Man5GlcNAc2-PP-dolichol (needed to synthesize

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

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

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

192 Autoantibodies to glycans present on glycolipids mediate the postinfectious paralytic disease

193 We evaluated how glycolipid-mediated activation of invariant natural kill

194 metabolism at three different points in the glycolipid metabolic cascade.

195 rected mutagenesis, and binding studies with glycolipid mimics have been used to define an extended b

196 Because in PNH the biosynthesis of the glycolipid molecule glycosylphosphatidylinositol (GPI) i

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

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

199 Glycoproteins and glycolipids of some mammalian species contain the disacc

200 wed that blocking binding of Ply to the sLeX glycolipid on RBCs prevents deposition of the toxin in t

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

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

203 1-ganglioside bridges arising from preformed glycolipid patches cross-link the complexes.

204 Catabolic enzymes of the ceramide and glycolipid pathway tightly control the amount of these a

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

206 Glycolipid-peptide conjugate vaccines may prove useful f

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

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

209 Concordantly, the related phenolic glycolipids (PGLs) promote the recruitment of permissive

210 Glycan structures on glycoproteins and glycolipids play critical roles in biological recognitio

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

212 2 and interferon-beta in the context of both glycolipid presentation and Toll-like receptor-mediated

213 After glycolipid presentation, these dendritic cells rapidly a

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

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

216 live pathogens, they do respond to bacterial glycolipids presented by CD1d on liver macrophage that h

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

218 ory T cells, respond to structurally diverse glycolipids presented by CD1d.

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

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

221 nthesis proteins, YpfP and LtaA, involved in glycolipid production, and LtaS, required for LTA backbo

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

223 Glycolipid-reactive T cells expressed memory markers and

224 Thus, Vdelta3 T cells are glycolipid-reactive T cells with distinct Ag specificiti

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

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

227 Anti-glycolipid reactivity was studied in patients with Guill

228 orientation and directly competing with the glycolipid receptor binding site on the surface of the B

229 and five B subunits that bind to a specific glycolipid receptor on host cells.

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

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

232 n human iNKT and Tregs upon pathogen-derived glycolipid recognition that has a significant impact on

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

234 The Stx2a subtype requires glycolipid residues in addition to Pk.

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

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

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

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

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

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

241 Invariant NKT (iNKT) cells are glycolipid-specific innate lymphocytes emerging as criti

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

243 GSL, reminiscent of cells from patients with glycolipid storage diseases.

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

245 dase activity and protein levels and reduced glycolipid storage.

246 idobacteria is the first step in correlating glycolipid structure with biological activity.

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

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

249 t was previously thought that recognition of glycolipids such as alpha-galactosylceramide (alpha-GalC

250 own a distinct mode of recognition of a self-glycolipid sulfatide bound to CD1d by a type II NKT TCR.

251 ocus is similar to that of another trehalose glycolipid, sulfolipid 1.

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

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

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

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

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

257 en length in the lipopolysaccharide (LPS), a glycolipid that forms most of the outer leaflet of the o

258 Lipid A is a glycolipid that serves as the hydrophobic anchor of LPS

259 pids into matrix lipids; (ii) preparation of glycolipids that aggregate to liposomes and micelles and

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

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

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

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

264 drate antigens (TACAs) and immunostimulatory glycolipids that hold promise as immunotherapeutics.

265 eromeric complexes are structurally distinct glycolipids that interact to form new molecular shapes c

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

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

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

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

270 e C-type lectin Mincle as receptor for these glycolipids that triggers the FcRgamma-Syk-Card9 pathway

271 en implicated in producing complex cell wall glycolipids, the biological function of PKS11 is unknown

272 g strategy to generate strong Th1-polarizing glycolipids through increased binding either to CD1d or

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

274 traction of the lipid-microdomain preferring glycolipid to the lo phase, while the phospholipid remai

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 use the coordinated action of two cell wall glycolipids to regulate macrophage recruitment to initia

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

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

280 y identifies CPTP as the prototype for a new glycolipid transfer protein fold subfamily.

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

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

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

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

285 trated that recognition of the mycobacterial glycolipid trehalose dimycolate (cord factor) by the C-t

286 (TdmhMtb) that hydrolyzes the mycobacterial glycolipid trehalose dimycolate and plays a critical rol

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

288 erium tumefaciens accumulates four different glycolipids under phosphate deficiency, including digala

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

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

291 lectin mincle to trehalose dimycolate, a key glycolipid virulence factor on the surface of Mycobacter

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

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

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

295 nd can recognize both alpha- and beta-linked glycolipids, whereas type II NKT cells are less well stu

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

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

298 Glycolipids with alpha-linked anomeric carbohydrates hav

299 yl cyclophosphatidic acid and a mixed acetal glycolipid, with the latter subsequently being isolated

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