ライフサイエンスコーパス: ferricytochrome c

1 by a spectrophotometric assay (reduction of ferricytochrome C).

2 ide dismutase (SOD)-inhibitable reduction of ferricytochrome c.

3 ease was measured by use of the reduction of ferricytochrome c.

4 catalytic oxidation of ferrocytochrome c to ferricytochrome c.

5 ne such molecule, the A-state of yeast iso-1-ferricytochrome c.

6 uperoxide dismutase-inhibitable reduction of ferricytochrome C.

7 amagnetic ferrocytochrome c and paramagnetic ferricytochrome c.

8 directly cross-linked to the basic patch in ferricytochrome c.

9 spiratory burst was measured by reduction of ferricytochrome C.

10 uperoxide dismutase-inhibitable reduction of ferricytochrome c, 2) monitoring fluxes in Ca2+ concentr

11 One exception to this is ferricytochrome c(552) from Hydrogenobacter thermophilus

12 lysis of NMR line shapes for H. thermophilus ferricytochrome c(552) is performed.

13 icytochrome c, while for CcP-complexed iso-1-ferricytochrome c, 70% of heme proton assignments were m

14 ption of the compact acid-denatured state of ferricytochrome c (A-state).

15 most frequently used scavengers of O(2)(*-), ferricytochrome c and Cu/Zn-SOD, were evaluated as compe

16 ow kinetic studies of azide binding to human ferricytochrome c and its Gly41Ser variant, together wit

17 the presence of saturating concentrations of ferricytochrome c and L-lactate, the catalytic cycle pro

18 relevant redox protein complex between yeast ferricytochrome c and yeast ferricytochrome c peroxidase

19 t activated cell sorter (FACS), reduction of ferricytochrome C, and bioassay, respectively.

20 with superoxide (O2*-) were estimated, using ferricytochrome c as a competitive inhibitor.

21 e 695 nm charge transfer band of horse heart ferricytochrome c as a function of pH between 7.0 and 10

22 e heme environment in bovine and horse heart ferricytochrome c as a function of temperature between 2

23 persed granuloma cells were unable to reduce ferricytochrome c (as an indicator of O2.-) in response

24 elevance for characterizing the structure of ferricytochrome c bound to anionic phospholipids.

25 uperoxide dismutase-inhibitable reduction of ferricytochrome c by myocyte monolayers.

26 mation of 19 complexes involving yeast iso-1-ferricytochrome c (Cc) and ferricytochrome c peroxidase

27 m catalyzes irreversible oxidative damage to ferricytochrome c (Cc3+) in the presence of H2O2 and 3,4

28 in, we demonstrate that unfolded horse heart ferricytochrome c (Cyt c) is a novel chromophoric probe

29 Horse ferricytochrome c (cyt c) undergoes exchange of one of i

30 en-am)-Cys-(Glu)(5)-Gly](3-) = RuCE(5)G, and ferricytochrome c = Cyt c.

31 ptor is either cupriplastocyanin, pc(II), or ferricytochrome c, cyt(III); and the mobile charge carri

32 We discuss our results in relation to ferricytochrome c folding kinetics.

33 granuloma cells, they also failed to reduce ferricytochrome c following PMA stimulation, implying th

34 onic circular dichroism (ECD) of horse heart ferricytochrome c for the Soret and 695 nm charge-transf

35 el for the solution structure of horse heart ferricytochrome c has been determined by nuclear magneti

36 Tuna ferricytochrome c has been used to demonstrate the poten

37 omparison of native and non-native states of ferricytochrome c has thus far not been achieved.

38 e alkaline-induced structural transitions of ferricytochrome c have been studied intensively as a mod

39 cedure, complete heme proton assignments for ferricytochrome c have never been demonstrated by a sing

40 e organism assay for their ability to reduce ferricytochrome c in a superoxide dismutase-inhibitable

41 sugars to solutions of acid-denatured equine ferricytochrome c induces formation of the A-state in th

42 e variants of Saccharomyces cerevisiae iso-1 ferricytochrome c (labeled at mutant Cys residues 4, 39,

43 The results indicated that the iso-1-ferricytochrome c magnetic axis system orientation shift

44 lving yeast iso-1-ferricytochrome c (Cc) and ferricytochrome c peroxidase (CcP).

45 rmation of the horse ferricytochrome c/yeast ferricytochrome c peroxidase complex.

46 ng of yeast iso-1-ferricytochrome c to yeast ferricytochrome c peroxidase in dilute solution and in s

47 y defined cytochrome c binding site on yeast ferricytochrome c peroxidase.

48 ex between yeast ferricytochrome c and yeast ferricytochrome c peroxidase.

49 easured with the use of superoxide-dependent ferricytochrome c reduction and flow cytometry with dihy

50 However, Cu(2+) inhibits ferricytochrome c reduction by the full-length nNOS 2 or

51 Cu(2+) and Zn(2+) also inhibit ferricytochrome c reduction by the independent reductase

52 NADPH oxidation by the full-length nNOS and ferricytochrome c reduction by the reductase domain are

53 uld then promote the selective inhibition of ferricytochrome c reduction in full-length nNOS.

54 Serum-induced ferricytochrome c reduction, cellular proliferation, and

55 ronal nitric-oxide synthase (nNOS) including ferricytochrome c reduction, NADPH oxidation, and citrul

56 and superoxide dismutase (SOD)--inhibitable ferricytochrome c reduction, respectively.

57 escence and superoxide dismutase-inhibitable ferricytochrome c reduction, respectively.

58 ultures via superoxide dismutase-inhibitable ferricytochrome c reduction.

59 generation, but rather was interfering with ferricytochrome c reduction.

60 rosomal ferrocytochrome b5, with horse heart ferricytochrome c, respectively.

61 on that pre-steady-state flavin oxidation by ferricytochrome c takes place at 120 s-1.

62 sfer reaction between ferrocytochrome b5 and ferricytochrome c that yields ferricytochrome b5 and fer

63 otochemical electron injection into unfolded ferricytochrome c titrated with 2.3 to 4.6 M guanidine h

64 We used yeast iso-1-ferricytochrome c to test for an evolutionary-invariant

65 thalpy change for the binding of yeast iso-1-ferricytochrome c to yeast ferricytochrome c peroxidase

66 The heme group in paramagnetic (S = 1/2) ferricytochromes c typically displays a markedly asymmet

67 global and local stabilities of a eukaryotic ferricytochrome c variant with an engineered disulfide a

68 The structure of encapsulated ferricytochrome c was determined to high precision (<r.m

69 When ferricytochrome c was entrapped within liposomes prepare

70 free and cytochrome c peroxidase-bound iso-1-ferricytochrome c were elucidated.

71 uperoxide dismutase-inhibitable reduction of ferricytochrome c were not different between cultured tr

72 nts have been made for wild-type yeast iso-1-ferricytochrome c when it is free in solution and when i

73 sonance assignments were made for free iso-1-ferricytochrome c, while for CcP-complexed iso-1-ferricy

74 used to investigate the interaction of horse ferricytochrome c with baker's yeast cytochrome c peroxi

75 compared to those for formation of the horse ferricytochrome c/yeast ferricytochrome c peroxidase com