ライフサイエンスコーパス: cholesterol oxidase

1 with a lipid bilayer membrane incorporating cholesterol oxidase.

2 ains accessible to treatment with the enzyme cholesterol oxidase.

3 ted by increased susceptibility to exogenous cholesterol oxidase.

4 o HDL, and the sensitivity of membrane FC to cholesterol oxidase.

5 ced by increased susceptibility to exogenous cholesterol oxidase.

6 ity of membrane cholesterol to extracellular cholesterol oxidase.

7 rturbation using methyl-beta-cyclodextrin or cholesterol oxidase.

8 ility of this membrane fraction to exogenous cholesterol oxidase.

9 tigate the membrane disruption properties of cholesterol oxidase.

10 membrane cholesterol was also measured using cholesterol oxidase.

11 rane cholesterol to enzymatic oxidation with cholesterol oxidase.

12 The crystal structure of cholesterol oxidase, a 56kDa flavoenzyme was anisotropic

13 ntially more rapidly than ent-cholesterol by cholesterol oxidase, a protein that contains a specific

14 lesterol through methyl-beta-cyclodextrin or cholesterol oxidase abolished the protective effect of C

15 n binding without substantially altering the cholesterol oxidase-accessible cellular [(3)H]cholestero

16 Cholesterol oxidase and cholesterol esterase were assemb

17 ensing platform was developed by integrating cholesterol oxidase and cholesterol esterase with the hy

18 and fibroblasts were used: susceptibility to cholesterol oxidase and cholesterol transfer to cyclodex

19 o crucial redox enzymes for biosensors (i.e. cholesterol oxidase and glucose oxidase) are targeted.

20 (This was gauged by its susceptibility to cholesterol oxidase and its rate of transfer to cyclodex

21 sterol with two cholesterol-specific probes, cholesterol oxidase and saponin.

22 experiments before and after incubation with cholesterol oxidase and sphingomyelinase show that these

23 Wild-type and E361Q cholesterol oxidases bind to vesicles with an apparent K

24 Our results indicate that cholesterol oxidase can metabolize phytosterols in vivo

25 We investigated the dependence of cholesterol oxidase catalytic activity and membrane affi

26 Cholesterol oxidase catalyzes the oxidation and isomeriz

27 Cholesterol oxidase catalyzes the oxidation and isomeriz

28 tobacco (Nicotiana tabacum) plants with the cholesterol oxidase choM gene and expressed cytosolic an

29 Cholesterol oxidase (ChOx) and catalase (CAT) were co-im

30 ose oxidase (GOx), lactate oxidase (LOx) and cholesterol oxidase (ChOx) by a new electron shuttling m

31 f H2O2 in the presence of O2/cholesterol and cholesterol oxidase (ChOx) by the fluorescence response

32 Furthermore, cholesterol oxidase (ChOx) is attached to G/PVP/PANI-mod

33 Cholesterol oxidase (ChOx), a member of the glucose-meth

34 Cholesterol oxidase (COase) is a bacterial enzyme cataly

35 olution at 37 degrees C by using an improved cholesterol oxidase (COD) activity assay.

36 acting enzyme was examined using a bacterial cholesterol oxidase (COD) as a model.

37 ng enzymes was addressed using soil bacteria cholesterol oxidase (COD) as a model.

38 ramide was investigated at 37 degrees C by a cholesterol oxidase (COD) reaction rate assay and by opt

39 total cholesterol using cholesterol esterase/cholesterol oxidase coupled with the luminol-H2O2-horser

40 The crystal structure of the redox enzyme cholesterol oxidase, determined at sub-angstrom resoluti

41 Transgenic leaf tissues expressing cholesterol oxidase exerted insecticidal activity agains

42 Degrading cholesterol in one monolayer with cholesterol oxidase first caused the boundary of the raf

43 eralfold; exposing the cells to mevinolin or cholesterol oxidase had the opposite effect.

44 e function of an active site loop (70-90) of cholesterol oxidase has been ascertained by deleting fiv

45 A neutron diffraction study of cholesterol oxidase has revealed an unusual elongated ma

46 The atomic resolution structure of cholesterol oxidase has revealed the presence of hydroge

47 lipid-modified surface, and incorporation of cholesterol oxidase in the electrode-supported thiolipid

48 solid-ordered state, the binding affinity of cholesterol oxidase increases approximately 10-fold.

49 The present work and our previous study on cholesterol oxidase-induced sterol oxidation suggest tha

50 These results demonstrate that cholesterol oxidase interacts directly with the lipid bi

51 Cholesterol oxidase is covalently linked to an 11-mercap

52 We conclude that the activity of cholesterol oxidase is directly and sensitively dependen

53 genic plants expressing chloroplast-targeted cholesterol oxidase maintained a greater accumulation of

54 To elucidate the cholesterol oxidase-membrane bilayer interaction, a cyst

55 Cholesterol oxidase modified platinum microcavity electr

56 Experiments for direct contact between the cholesterol oxidase-modified electrode and the surface o

57 The cholesterol oxidase-modified electrodes show steady-stat

58 Enzymatic turnovers of single cholesterol oxidase molecules were observed in real time

59 cholesterol oxidation catalyzed by mediated cholesterol oxidase occurred at the anode.

60 Cholesterol oxidase represents a novel type of insectici

61 n with methyl-beta-cyclodextrin, filipin, or cholesterol oxidase resulted in an insulin-independent i

62 rs cholesterol within the membranes, or with cholesterol oxidase resulted in markedly reduced galanin

63 timulate the interaction of cholesterol with cholesterol oxidase, saponin and cyclodextrin, presumabl

64 e X-ray crystal structure of the flavoenzyme cholesterol oxidase, SCOA (Streptomyces sp.SA-COO) has b

65 The loss of the cholesterol oxidase-sensitive FC pool and FC efflux to s

66 small unilamellar vesicles and an increased cholesterol oxidase-sensitive pool of membrane FC on the

67 spholipid vesicle acceptors and an increased cholesterol oxidase-sensitive pool of membrane free chol

68 a greatly reduced ability to: 1) enlarge the cholesterol oxidase-sensitive pool of membrane free chol

69 nspection of the X-ray crystal structures of cholesterol oxidase suggested that an active-site "lid"

70 hatidylcholine, previously shown to decrease cholesterol oxidase susceptibility, reduced the transfer

71 The binding affinities of cholesterol oxidase to 100-nm unilamellar vesicles compo

72 differences were abolished by treatment with cholesterol oxidase to disrupt membrane rafts.

73 DHE ester synthesis is achieved by employing cholesterol oxidase to selectively render unesterified D

74 Thus, binding of cholesterol oxidase to the membrane and partitioning of

75 Cholesterol oxidase was immobilized in a sol-gel matrix

76 the sensitivity of cellular FC to exogenous cholesterol oxidase was tested under conditions in which

77 This acrylodan-labeled cholesterol oxidase was used to explore the pH, ionic st

78 rs that contain GOx, L-amino acid oxidase or cholesterol oxidase wherein the intrinsic FAD fluorescen

79 -one and therefore mimicking the activity of cholesterol oxidase, which is implicated in cardiovascul