ライフサイエンスコーパス: difference spectra

1 he catalytic mechanism of DrrA from the FTIR difference spectra.

2 positive and negative bands observed in the difference spectra.

3 taking the difference between the above two difference spectra.

4 it an initial anisotropy in their absorption difference spectra.

5 t of heme proteins observed in mitochondrial difference spectra.

6 is a large change in the resulting far-UV CD difference spectra.

7 clearly observed by monitoring the protein's difference spectra.

8 ions (1800-1200 cm(-)(1)) of any of the FTIR difference spectra.

9 endent IR features in reduced minus oxidized difference spectra.

10 ve assignments of vibrations observed in our difference spectra.

11 egions (1800-1000 cm(-1)) of any of the FTIR difference spectra.

12 e for the presence of a cysteine mode in our difference spectra.

13 cal displays of experimental, calculated and difference spectra.

14 ons had large effects on P(M) minus oxidized difference spectra.

15 by comparing experimental and theoretical IR difference spectra.

16 considerably alters the (P700(+)-P700) FTIR difference spectra.

17 From the time-resolved and static FTIR difference spectra, A(1)(-)/A(1) FTIR difference spectra

18 Raman difference spectra acquired at different metal ion condi

19 effect on these rates, and the Y(Z)* - Y(Z) difference spectra all depend on pH (from 5.5 to 9.5).

20 fication of HSAP led to the development of a difference spectra analysis program (DSAP) which was use

21 nNOS to produce light-induced CO photolysis difference spectra and to compare spectra after hydrogen

22 Difference spectra and Western blot analysis showed norm

23 addition, the electrochemically induced FTIR difference spectra are compared for preparations of the

24 ng of PS I, however, the (P700(+)-P700) FTIR difference spectra are considerably altered.

25 The nu(NO) modes from the light-induced FTIR difference spectra are isolated from other perturbed vib

26 The time-resolved IR difference spectra are markedly different to those of wt

27 Importantly, the first and second flash difference spectra are reproduced in the 1800-1200 cm(-)

28 ligand modes, and the difference and double-difference spectra are used in identifying Mn-O bridging

29 These IR redox difference spectra arise from perturbations of prostheti

30 Photoaccumulated Fourier transform infrared difference spectra associated with P700(+) and P700(+)A(

31 lecular mechanics) methods to calculate FTIR difference spectra associated with protein-bound cofacto

32 a computational-based interpretation of FTIR difference spectra associated with protein-bound cofacto

33 roach we have calculated isotope edited FTIR difference spectra associated with unlabeled and labeled

34 Reaction-induced difference spectra, associated with the reduction of Y12

35 Static P700(+)/P700 FTIR difference spectra at 77 K were also obtained for all of

36 of the active protein was observed by Raman difference spectra at low concentrations which features

37 In this work, reduced minus oxidized difference spectra at pH 6.5 and 9.0 and P(M) minus oxid

38 ra at pH 6.5 and 9.0 and P(M) minus oxidized difference spectra at pH 9.0 were compared in unlabeled,

39 Analysis of the CD difference spectra at three wavelengths yielded an estim

40 Difference spectra based on isotope editing, a technique

41 UV resonance Raman difference spectra between ligated and deoxyhemoglobin c

42 The UVRR difference spectra between rhodopsin and mearhodopsin I

43 The UVRR difference spectra between rhodopsin and metarhodopsin I

44 Calculation of the CD difference spectra (bound minus free) of stoichiometrica

45 Isotope difference spectra clearly show that the heme group in t

46 Time-resolved optical absorption difference spectra collected between 373 and 521 nm were

47 l reduction of 3a-c in situ afforded optical difference spectra consistent with the formation of the

48 Simulated difference spectra, corresponding to the global folding

49 minor spectral changes that, based on flavin difference spectra defined in the presence of 3OHKyn, ca

50 One-dimensional NOE difference spectra demonstrate that G.T mismatches form

51 as reacted with SHV-1 in solution, the Raman difference spectra demonstrated that only a major popula

52 rum (DAS) from global analysis of absorption difference spectra excited at 660 nm is essentially flat

53 Voltage dependence of difference spectra exhibit a crossover point near the pe

54 dazole and 1-phenylimidazole yielded type II difference spectra exhibiting Kd values of 63 +/- 2 and

55 binding was explored by analyzing the Raman difference spectra for [D5 + Mg(2+)] minus [D5 no Mg(2+)

56 calculate the "anion minus neutral" infrared difference spectra for both phylloquinone and its methyl

57 ions to produce anion minus neutral infrared difference spectra for both phylloquinone and plastoquin

58 The Raman difference spectra for each of the inhibitors in the E16

59 By comparison of the theoretical IR-difference spectra for magnesium ion coordinated triphos

60 spectroscopy we have produced A1(-)/A1 FTIR difference spectra for menB, menD, and menE photosystem

61 ly 1414(+) cm(-)(1) in the A(1)(-)/A(1) FTIR difference spectra for photosystem I particles from both

62 arison of the experimental spectra and model difference spectra for the intramolecular electron trans

63 We measured the light-minus-dark FTIR difference spectra for the LOV2 domain of oat phot1.

64 1)(-)/A(1) Fourier transform infrared (FTIR) difference spectra for these menB photosystem 1 particle

65 Difference spectra for three singly oxidized P450-BM3 in

66 om temperature (wild-type-mutant) absorption difference spectra for trimeric mutants lacking the PsaF

67 FTIR spectroscopy to compare Q(A)(-)/Q(A) IR difference spectra for wild type and the M265 mutant RCs

68 Raman difference spectra from crystals with the substrate boun

69 The IR and VCD difference spectra further confirm the assignment of all

70 ed (EH2) species, and oxidized minus reduced difference spectra give maxima and minima at 41.3 and 30

71 0(+)-P700) Fourier transform infrared (FTIR) difference spectra have been obtained using photosystem

72 displayed typical cytochrome P450 (P450) CO-difference spectra; however, the Asn404Tyr and Ile192Asn

73 used to produce P700(+)A(1)(-)/P700A(1) FTIR difference spectra in intact photosystem I particles fro

74 mine MRS peaks were resolved from MEGA-PRESS difference spectra in prefrontal, occipital, and subcort

75 e all of the mutation induced changes in the difference spectra in terms of difference band assignmen

76 First, FTIR difference spectra in the amide I vibrational band (1600

77 between actin activation and ATP versus ADP difference spectra in the presence of various metal ions

78 We measured time-resolved difference spectra, in the visible and the infrared, for

79 The difference spectra include those of PGK-ATP minus PGK, P

80 ajority of these inhibitors elicited type II difference spectra indicating the formation of a coordin

81 ncy feature does not appear in the cryogenic difference spectra, indicating that the perturbation is

82 te is generated with kinetics and associated difference spectra indicative of vibrational cooling wit

83 ion, the R108F mutation abrogated the Type I difference spectra induced by flurbiprofen and benzbroma

84 In contrast, Raman difference spectra involving the product, propionyl-CoA,

85 of mutant and wild type (P700(+)-P700) FTIR difference spectra, it is shown that (1) the 13(3) ester

86 UV difference spectra measured for the respective enzyme-li

87 ant change in electrochemically induced FTIR difference spectra measured in the presence and absence

88 ype, the mutant A(1)(-) (FeS) - A(1)(FeS)(-) difference spectra, measured in cells and photosystem I

89 Difference spectra (mutant minus control) of all the mut

90 In (reduced) minus (reduced plus CO) difference spectra, negative bands at 1931 and 1907 cm(-

91 Difference spectra observed for the aromatic carboxylate

92 In A(1)(-)/A(1) FTIR difference spectra obtained for unlabeled photosystem I

93 The A(1)(-)/A(1) FTIR difference spectra obtained for unlabeled trimeric photo

94 s mutant is indistinguishable from published difference spectra obtained for wild-type bacteriorhodop

95 We report ATR-FTIR difference spectra obtained from both low- and high-pH f

96 Furthermore, we now compare difference spectra obtained in H2O and D2O as our first

97 Fourier transform infrared difference spectra obtained in various spectral regions

98 Difference spectra obtained over time isolate contributi

99 The ultraviolet resonance Raman (UVRR) difference spectra obtained reveal that E helix motion i

100 Comparison of (P700(+) - P700) FTIR difference spectra obtained using PS I particles from th

101 A1(-)/A1 FTIR difference spectra, obtained using menB mutant photosyst

102 Raman difference spectra of 4-NBA-CoA and 4-FBA-CoA bound to W

103 heme at room temperature, time-resolved FTIR difference spectra of bacteriorhodopsin, including the w

104 We have now measured time-resolved FT-IR difference spectra of bR intermediates in the wild-type

105 Redox difference spectra of center N2, together with substrate

106 Time-resolved absorption difference spectra of COS-cell expressed rhodopsin and r

107 supported by electrochemically induced FTIR difference spectra of cytochrome bd in the presence of t

108 TR-FTIR method has been used to record redox difference spectra of cytochrome c oxidase in the unliga

109 Cytochrome difference spectra of everted membrane vesicles from the

110 For the protein complexes, the Raman difference spectra of flavin bound to wt PHBH and wt PHB

111 Here we used newly determined difference spectra of individual components to resolve t

112 IR and visible redox difference spectra of iron-sulfur protein/cytochrome c(1

113 r protein which in turn allowed the IR redox difference spectra of ISP and cytochrome c(1) to be deco

114 Time-resolved absorption difference spectra of membrane suspensions of bovine rho

115 Metal-dependent difference spectra of Ni(II)- and Cu(I)-InrS are similar

116 n bands are resolved in the light-minus-dark difference spectra of oxygen-evolving PS II core complex

117 peptide bonds in bR are assigned from REDOR difference spectra of pairwise labeled samples, and corr

118 -frequency (670-350 cm(-)(1)) S(2)/S(1) FTIR difference spectra of photosystem II (PSII) particles is

119 group that gives rise to this band, the FTIR difference spectra of PSII core complexes from the mutan

120 The resultant S(2)-minus-S(1) FTIR difference spectra of purified wild-type and mutant PSII

121 or helices 3 and 6, time-resolved absorption difference spectra of rhodopsin mutants G121A, G121V, an

122 athochromic intermediates and the normalized difference spectra of the batho-shifted intermediates of

123 modes near 1520 cm(-1) in each of the Raman difference spectra of the five complexes examined unambi

124 "Light"-minus-"dark" FTIR difference spectra of the fully reduced CO-enzyme adduct

125 e-resolved Fourier transform infrared (FTIR) difference spectra of the halorhodopsin (hR) photocycle

126 Electrochemically induced FTIR difference spectra of the inactive D75H mutant enzyme sh

127 --> S2, and S2 --> S3 transitions, the FTIR difference spectra of the individual S state transitions

128 these hypotheses, we have compared the FTIR difference spectra of the individual S state transitions

129 (2), and S(2) --> S(3) transitions, the FTIR difference spectra of the individual S-state transitions

130 Difference spectra of the labeled minus unlabeled oxidiz

131 The S(2)-minus-S(1) FTIR difference spectra of the purified PSII particles show t

132 The UVRR difference spectra of the sensor domain displayed a posi

133 his secondary structure are prominent in the difference spectra of the substrate complex.

134 The difference spectra of the W35F and W175F mutants were id

135 Overall redox difference spectra of the wild type and M183K mutant wer

136 Both in vivo and in vitro difference spectra of this phytochromic species are very

137 Appearance in infrared photoperturbation difference spectra of virtually all bands previously rep

138 The light-induced difference spectra of whole cells, membranes, and the is

139 that the mid-frequency (1800-1200 cm-1) FTIR difference spectra of wild-type and D1-D342N PSII partic

140 Fluorescence difference spectra of wild-type and P1 tryptophan varian

141 e step, we have measured time-resolved FT-IR difference spectra of wild-type bR containing either nat

142 uction is found for the near-UV spectra (and difference spectra) of mutants involving aromatic amino

143 In addition, the Raman difference spectra often contain contributions from prot

144 Electrochemically induced FTIR difference spectra on the highly conservative D75E mutan

145 Low-temperature FTIR difference spectra on these core-deuterated samples reve

146 CO difference spectra performed with extracts of cells grow

147 These Y122O(*) minus Y122OH difference spectra provide evidence that the Y122OH redo

148 For the carboxylated 1.3S, the difference spectra provided the vibrational signature of

149 >M FTIR difference spectra recorded for unlabeled and selenometh

150 Light-induced difference spectra, recorded in the 350-700 nm region ov

151 tial fitting of the time-resolved absorption difference spectra resolved five apparent lifetimes.

152 spectral region by the fifth and sixth flash difference spectra, respectively.

153 t interface are diminished, and at pH 9, the difference spectra reveal a shift to the R quaternary st

154 UV difference spectra reveal environmental alterations of a

155 Difference spectra reveal that 18 of 29 histidine residu

156 Absorbance difference spectra reveal that a single protonation stat

157 The difference spectra reveal that following ultraviolet A e

158 cose and saline solutions; after each cycle, difference spectra reveal that the partitioning process

159 Difference spectra revealed that monodentate complexes a

160 At a 4.9 M excess of the NH2 terminus the difference spectra shifted to what was predominately a b

161 The light-induced difference spectra show a peak at 438 nm and a trough at

162 The difference spectra show that complete partitioning and d

163 Raman difference spectra show that conformational changes occu

164 on of (P740(+)-P740) and (P700(+)-P700) FTIR difference spectra show that P700 and P740 share many st

165 Raman difference spectra show that the beta subunit binds to b

166 These difference spectra show that the P700 triplet state ((3)

167 The Raman difference spectra show that this mutation does not affe

168 The P700/P700+. optical difference spectra show the appearance of a new bleachin

169 Difference spectra show the covalent intermediate has an

170 inic acid bound to the enzyme to give type I difference spectra similar to that of L-Arg.

171 ing becomes invisible as monitored by UV-vis difference spectra since the spectral reporters Tyr188 a

172 able to identify bands in A(1)(-)/A(1) FTIR difference spectra that are due to the carbonyl (C=O) mo

173 signatures are apparent in the picosecond IR difference spectra that would correspond to alteration i

174 tion of both type I and type II perturbation difference spectra; the former involves displacement of

175 te and use IC(50) or K(i) values and optical difference spectra to quantitate their affinity relative

176 Changes in the FTIR difference spectra upon photoconversion of the M interme

177 Previously, we have obtained A1(-)/A1 FTIR difference spectra using labeled and unlabeled photosyst

178 Addition of erythromycin generates substrate difference spectra using microsomes from rats treated wi

179 by analysis of the pH dependencies of redox difference spectra using perfusion/electrochemically ind

180 Steady state correlated difference spectra (W21F-W21F:Y9F) have been used to obt

181 An alternative method based on analyzing IR difference spectra was also introduced to obtain thermod

182 Light-minus-dark difference spectra were acquired, monitoring structural

183 Absorption difference spectra were collected after excitation with

184 Time-resolved optical absorption difference spectra were collected at delay times from 10

185 ions in receptor photoactivation, absorbance difference spectra were collected at time delays from 30

186 olyzed at 20 degreesC with 477 nm light, and difference spectra were collected at time delays ranging

187 Time-resolved optical absorption difference spectra were collected by a gated multichanne

188 c FTIR difference spectra, A(1)(-)/A(1) FTIR difference spectra were constructed.

189 These IR difference spectra were distinctly different from the IR

190 The changes in the UV difference spectra were exploited to assess directly the

191 Nanosecond photolysis difference spectra were measured in the visible bands of

192 Raman difference spectra were obtained by subtracting the spec

193 quantitatively similar transient absorption difference spectra were obtained; the only distinguishin

194 Absorbance difference spectra were recorded at 20 degrees C from 30

195 Absorbance difference spectra were recorded at 20 degrees C with a

196 Absorbance difference spectra were recorded at a sequence of time d

197 Absorbance difference spectra were recorded from 20 ns to 1 micros

198 Visible difference spectra were recorded synchronously using a l

199 FTIR difference spectra were used also to follow spontaneous

200 The integrated absorbance difference spectra (when normalized to the total PS I Qy

201 CYP3A43 gave a reduced carbon monoxide difference spectra with an absorbance maximum at 450 nm.

202 l-1,2,3-thiadiazole shows type I and type II difference spectra with P450s 2B4 and 2E1, respectively,