ライフサイエンスコーパス: mannoprotein

1 neoformans lysate, and purified cryptococcal mannoprotein.

2 t multiple mannose receptors on DC recognize mannoprotein.

3 (CD209) was determined to have affinity for mannoprotein.

4 ponents of the N-linked glycans of cell wall mannoprotein.

5 ivo is beta(1-->3)glucan, beta(1-->6)glucan, mannoprotein.

6 l has three of the main components but lacks mannoprotein.

7 e that could remove N-acetylglucosamine from mannoproteins.

8 f substrates involved in the biosynthesis of mannoproteins.

9 yeast protein extracts (YPE), cell walls and mannoproteins.

10 dependent on heavily mannosylated Ags termed mannoproteins.

11 particular epithelial cells and to aggregate mannoproteins.

12 hought to be comprised, at least in part, of mannoproteins.

13 tracellular changes arising from the loss of mannoproteins.

14 l in an och1 mutant that does not synthesize mannoproteins.

15 lacked terminal N-acetylglucosamine in their mannoproteins.

16 are substrates in the biosynthesis of these mannoproteins.

17 h lacked terminal N-acetylglucosamine in its mannoproteins.

18 3, corresponded to the high concentration of mannoproteins, 2-phenyl ethanol and tyrosol.

19 rich in arabinose and galactose (39-54%) and mannoproteins (38-55%) were the major PS in the base win

20 ronoxylomannan (GXM), galactoxylomannan, and mannoprotein, affect expression of molecules on the surf

21 ally studied after isolating its components (mannoproteins, alpha1,3-glucan, beta1,3-glucan, and a br

22 es the complete structure of a mycobacterial mannoprotein and the first complete structure of a manno

23 and previous findings on the linkage between mannoproteins and beta(1-->6)-glucan, it is concluded th

24 in the incorporation of label into cell wall mannoproteins and beta(1-->6)glucan was observed.

25 accharides, with different behaviors between mannoproteins and beta-glucans.

26 cross-linking between beta-1,6-glycosylated mannoproteins and chitin.

27 Candida, but recently specific antibodies to mannoproteins and hsp90 have been shown to be protective

28 ance of cell wall integrity and retention of mannoproteins and known cryptococcal virulence factors i

29 itation steps, and clear distinction between mannoproteins and other wine polysaccharides.

30 Mannoproteins and polysaccharides rich in arabinose and

31 t analysis (PCA) results, being stronger for mannoproteins and rhamnogalacturonan-II (RG-II), but onl

32 ompounds), with the functional groups of the mannoproteins and the free amino acids of the surface of

33 A mannoprotein antigen, MP98, that stimulated one of the h

34 ->3)-glucan, beta(1-->6)-glucan, chitin, and mannoprotein are linked together.

35 Mannoproteins are major antigens driving T cell response

36 The mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere

37 Mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere

38 The mannan chains of Kluyveromyces lactis mannoproteins are similar to those of Saccharomyces cere

39 CWP1 and CWP2, the genes encoding the major mannoproteins, are down-regulated, suggesting that there

40 ucan is linked to both beta(1-->3)glucan and mannoprotein, as well as occasionally to chitin.

41 rium tuberculosis; however, the mechanism of mannoprotein assembly remains unclear.

42 rine DC rapidly captured fluorescent-labeled mannoprotein by a mannose receptor-mediated process.

43 at is dependent upon the efficient uptake of mannoprotein by mannose receptors.

44 Several cell wall mannoproteins can bind to immobilized osmotin, suggestin

45 ryptococcal transcript for the extracellular mannoprotein Cig1 is highly regulated by iron and abunda

46 Mitogen- and cryptococcal mannoprotein (CMP)-activated (CD25+CD134+) CD4+ T cells

47 Mannoprotein colocalized intracellularly with CD206 and

48 nthesis, it may participate in production of mannoprotein components of the capsule.

49 Differences in the mannoprotein composition of C. albicans A9 and four spon

50 us of C. albicans, we compared the cell wall mannoprotein content and composition between C. albicans

51 DS and with the significant reduction in the mannoprotein content of mutants compared with the wild-t

52 However, monitoring of mannoprotein content of wine during these processes, or

53 have been developed in order to increase the mannoprotein content of wine.

54 Thus, mannoproteins could be an effective alternative for prot

55 Additionally, some mannoproteins decreased the browning potential.

56 the absence of serum, galactoxylomannan and mannoprotein did not affect L-selectin, TNF receptor, CD

57 Treating yeast cells to remove cell wall mannoprotein did not reduce SP-D binding, and SP-D faile

58 zed the wines; however, some arabic gums and mannoproteins do not stabilized the wines.

59 or wine polyphenols or tannins and a YPE, a mannoprotein fraction and a beta-glucan were monitored b

60 otein, hexose, and phosphate contents of the mannoprotein fraction did not differ significantly among

61 tablished based upon the capacity of (i) the mannoprotein fraction of C. neoformans supernatants to s

62 The cell wall mannoproteins from hydrophilic and hydrophobic cells of

63 The DAN/TIR mannoprotein genes of Saccharomyces cerevisiae (DAN1, DA

64 is a complex structure consisting mainly of mannoproteins, glucan, and chitin.

65 Thus, a C. neoformans mannoprotein has been characterized that stimulates T ce

66 Thus, a second cryptococcal mannoprotein has been identified which stimulates T-cell

67 omyces cerevisiae strain EKD13 overproducing mannoproteins has been used to obtain Albarino white win

68 es but affects color stability in red wines, mannoproteins have a variable effectiveness depending on

69 mouse bladder epithelial cells and a soluble mannoprotein, horseradish peroxidase, was contained with

70 The DAN/TIR genes encode nine cell wall mannoproteins in Saccharomyces cerevisiae which are expr

71 phatidylinositol anchor formation, prevented mannoprotein incorporation, whereas the beta(1-->3)-beta

72 a diffused cell wall with loss of the outer mannoprotein layer as compared with the WT cells.

73 aberrant cell wall structure with a reduced mannoprotein layer.

74 Candida albicans mannoprotein (MAN) administered intravenously to mice st

75 mannan (GXM), galactoxylomannan (GalXM), and mannoprotein (MP), to interact with CD18 on human PMN.

76 After adsorption, no antibodies specific to mannoprotein (MP)-rich extracts or secretions were detec

77 ined in the presence and absence of isolated mannoproteins (MP) and arabinogalactans (AG) from WPM.

78 Cryptococcal mannoproteins (MP) are highly mannosylated antigens whic

79 Soluble Cryptococcus neoformans mannoproteins (MP) have emerged as promising vaccine can

80 lin A affinity chromatography into adherent (mannoprotein [MP]) and nonadherent (flowthrough [FT]) fr

81 tatin nonaketide synthase [LNS], a cell wall mannoprotein [MP1], and a gene fragment of the cytochrom

82 In addition to the above defect in mannoproteins, mutant cells were also deficient in the b

83 The mannoprotein nature of MP88 was established based upon t

84 ch encodes a putative adhesin-like cell wall mannoprotein of C. albicans and radD, an arginine-inhibi

85 monoclonal antibody C7, a mAb directed to a mannoprotein of Candida albicans, significantly reduced

86 nts demonstrated that DC captured sufficient mannoprotein over 2 h to account for 50% of total stimul

87 o hyphae of a strain deficient in the fungal mannoprotein, Pra1.

88 tent of wine during these processes, or even mannoprotein quantification in the final wines, is an an

89 , we report a simple and accurate method for mannoprotein quantification in wines.

90 nd Mox2, and an activation factor, Mox4 (for mannoprotein regulation by oxygen).

91 Mannoproteins released by yeast cells throughout the win

92 f Saccharomyces cerevisiae encode homologous mannoproteins, some of which are essential for anaerobic

93 ells, and macrophages were used to stimulate mannoprotein-specific T cells.

94 were assessed following ex vivo cryptococcal mannoprotein stimulation, using 13-color flow-cytometry.

95 cell wall is enriched in highly glycosylated mannoproteins that are implicated in many aspects of the

96 potentially useful to produce wines rich in mannoproteins that have distinctive characteristics comp

97 individual oligomannosyl residues in Candida mannoprotein, the major antigenic determinant located on

98 Mannoproteins, the third major component of the cell wal

99 By confocal microscopy, intracellular mannoprotein trafficked to an endo-lysosomal compartment

100 together with prior work demonstrating that mannoprotein was captured by the macrophage mannose rece

101 ork presented, the innate immune response to mannoprotein was determined.

102 annosylation, an immunoreactive cryptococcal mannoprotein was expressed recombinantly in E. coli and

103 lomannan (GXM), but not galactoxylomannan or mannoprotein, was found to cause loss of L-selectin from

104 ind suitable alternatives, eleven commercial mannoproteins were chemically characterized concerning t

105 atile esters, dimethyl sulfide, glycerol and mannoproteins with harvest date.

106 f the cell wall is comprised of glycosylated mannoproteins with the majority of these post-translatio

107 Mannoprotein, with a protein moiety about 100 kDa in app