ライフサイエンスコーパス: fluorescence decay

1 e lifetimes by decreasing radiative rates of fluorescence decay.

2 a lower impact of the ultrafast component on fluorescence decay.

3 of anthocyanins in solution shortened their fluorescence decay.

4 olysis products, furan, were responsible for fluorescence decay.

5 of the brief lifetime component of the qBBr fluorescence decay.

6 g to noninducing conditions and by measuring fluorescence decay.

7 for the previously described monoexponential fluorescence decay.

8 onential terms describing the time-dependent fluorescence decay.

9 intermediates were observed from femtosecond fluorescence decays.

10 spectroscopy based on statistical fitting of fluorescence decays, 2D FCS can resolve species whose fl

11 om the analysis of the I(VV)(t) and I(VH)(t) fluorescence decays acquired with a standard time-resolv

12 he acquisition and analysis of time-resolved fluorescence decays acquired with a vertically polarized

13 400 nm to both steady-state fluorescence and fluorescence decay across picosecond and nanosecond time

14 Fluorescence decay after photoactivation (FDAP) and fluo

15 Ts in axon-like processes, we used a refined fluorescence decay after photoactivation approach and si

16 e, we observed by quantitative imaging using fluorescence decay after photoactivation recordings of p

17 This study introduces a global fluorescence decay analysis that substantially simplifie

18 ed in earlier work have little effect on the fluorescence decay and appear to occur away from the try

19 igated by experimental measurements of Trp37 fluorescence decay and compared with theoretical measure

20 troscopy revealed a strong dependence of the fluorescence decay and electron-transfer/charge-recombin

21 ntly fluorogen dissociation, leading to fast fluorescence decay and fluorogen-concentration-dependent

22 Q6H2 was found to prevent both fluorescence decay and generation of lipid peroxides (LO

23 The greater fluorescence decay and more rapid breakup for the high c

24 nce of LHCBM9 resulted in faster chlorophyll fluorescence decay and reduced production of singlet oxy

25 c studies (emission quenching, time-resolved fluorescence decay, and transient absorption spectroscop

26 The in-plane depolarized fluorescence decays are described by a stretched exponen

27 nce decays, 2D FCS can resolve species whose fluorescence decays are linked by the rate constants in

28 dsRed fluorescence decays as a single exponential with a 3.65

29 photophysical features of bilirubin make its fluorescence decay at picosecond time scale sensitive to

30 of Corti, we show that the time constants of fluorescence decay at the basolateral pole of IHCs and a

31 sion is spectrally isolated, analysis of the fluorescence decay can distinguish changes in membrane f

32 fluorescence lifetime; (2) amplitude of the fluorescence decay components; and (3) thylakoid membran

33 This was followed by a biexponential fluorescence decay containing fast and slow components,

34 rates were uncovered by deconvolution of the fluorescence decay curve.

35 ce spectroscopy (TRFS), i.e., measurement of fluorescence decay curves for different excitation and/o

36 In agreement with our conclusions, the fluorescence decay curves of 6-fluorotryptophan-containi

37 Fluorescence decay curves of each are monoexponential ex

38 Fluorescence decay curves were measured with high precis

39 r time divided by that of an earlier image), fluorescence decay curves, fluorescence decay rates, and

40 ed and fit-free analysis of multiexponential fluorescence decay curves.

41 Time-resolved fluorescence decay data for the Cu(I)-saturated probe in

42 ng global analysis to simultaneously fit the fluorescence decay data of all pixels in an image or dat

43 allows us to fit both the prompt and delayed fluorescence decay data quantitatively.

44 Fitting of the fluorescence decay data using the method of least square

45 (E), based on three-exponential fits to the fluorescence decay data, is 2.5 +/- 0.7% (SEM, N = 12).

46 icability of a rotamer model to describe the fluorescence decay data.

47 In monellin, the fluorescence decay displays multiexponential character w

48 The fluorescence decay due to photobleaching of the immobile

49 Fluorescence decay due to tangential flow would be expec

50 uire an accurate subnanosecond time-resolved fluorescence decay every 0.1 ms after stopped flow.

51 uorescence recovery after photobleaching and fluorescence decay experiments, we find that the stable

52 uch slower in the native rubredoxin; the Trp fluorescence decay extends to 10 ps and longer, reflecti

53 ed four kinetic components: an initial, fast fluorescence decay, followed by a transient increase, an

54 ingle crystals, we have established that the fluorescence decay function of AP shows a pronounced, ch

55 Analysis of the AP fluorescence decay function reveals conformational heter

56 The fluorescence decay functions of individual, specifically

57 sicle containing solutions, multiexponential fluorescence decays imply separate solute populations in

58 that does not require global fitting of the fluorescence decay in every spatial position of the samp

59 n the amplitude of the 60-70 ps component of fluorescence decay in open Chl b-containing PS II center

60 However, fluorescence decay in the presence of DCMU, which monito

61 peal of the phasor representation of complex fluorescence decays in biological systems is that a visu

62 Dual exponential fluorescence decay is assigned to the two conformers of

63 ly suggest that the extent of nonexponential fluorescence decay is governed primarily by the efficien

64 However, chlorophyll fluorescence decay kinetics after a single saturating fl

65 ins lacking photosystem I did not change the fluorescence decay kinetics after illumination, and ther

66 fer process was examined mechanistically via fluorescence decay kinetics and fluorescence anisotropy

67 The actual fluorescence decay kinetics can be fit to one exponentia

68 Fluorescence decay kinetics in the absence of DCMU indic

69 Fluorescence decay kinetics in the presence of DCMU indi

70 Trp4 fluorescence decay kinetics measured for the F4W protein

71 II (PSII), exhibits complex multiexponential fluorescence decay kinetics that for decades has been as

72 In this study, we have used fluorescence decay kinetics to quantitatively probe Phot

73 al processor allows extraction of the sample fluorescence decay kinetics without distortions which ca

74 ophan residue that exhibits multiexponential fluorescence decay kinetics, was also examined as a more

75 tensity by up to 500% and induce complicated fluorescence decay kinetics.

76 fast and slow components of the flash-probe fluorescence decay kinetics.

77 pseudo-first-order rate constant describing fluorescence decay (kobs) increases linearly with [cytoc

78 ce peak intensity at 390 nm (I(375)/I(390)), fluorescence decay lifetime (tau), or rotational correla

79 Independent fluorescence decay lifetime and rotational dynamics para

80 hat the bases are stacked; at the same time, fluorescence decay lifetimes are heterogeneous, indicati

81 rescent protein (GFPuv) that exhibit altered fluorescence decay lifetimes.

82 According to variable fluorescence decay measurements in DCMU-treated cells, c

83 ient absorption spectroscopy, and picosecond fluorescence decay measurements permits detailed analysi

84 Time-resolved fluorescence decay measurements upon Chl excitation show

85 dynamics were examined through time-resolved fluorescence decay measurements.

86 differs between different dyes; the initial fluorescence decay mirrors the loss of granule contents

87 ns typically entails fitting data to complex fluorescence decay models but such experiments are frequ

88 ich occurs within the mixing time; and 2), a fluorescence decay occurring between approximately 100 a

89 explanation for the unusual monoexponential fluorescence decay of 5-fluorotryptophan (5FTrp) in sing

90 We have analyzed the fluorescence decay of anthocyanins by fluorescence lifet

91 , a linear correlation was found between the fluorescence decay of BODIPY 581/591 C11 and the concent

92 In contrast, fluorescence decay of calcium-bound jRCaMP1a occurs by t

93 However, fluorescence decay of calcium-bound jRGECO1a follows a d

94 tive component (deltagamma(r)(-1)(t)) of the fluorescence decay of chromophores in proteins also is e

95 Oxidation-induced fluorescence decay of diphenylhexatriene-labeled phospha

96 Western blot analysis indicated that the fluorescence decay of EGFP-MODC-(422-461) was correlated

97 d relaxation of protein water to explain the fluorescence decay of monellin.

98 The fluorescence decay of Rev M11 delta 14 was resolved into

99 The fluorescence decay of the cis-W3 zwitterion was biexpone

100 The time-resolved fluorescence decay of the donor in each labeled junction

101 Fluorescence decay of the solute molecules is collected

102 provide compelling evidence that the complex fluorescence decay of the tryptophan zwitterion originat

103 Analysis of the donor fluorescence decay of the unfolded subpopulation of both

104 The fluorescence decay of Trp246 is a triple exponential wit

105 The fluorescence decay of Trp45 in wild-type Rev was resolve

106 the origin of the ubiquitous nonexponential fluorescence decay of tryptophan in proteins.

107 conducted whereby the I(VV)(t) and I(VH)(t) fluorescence decays of a series of oligoquinolines label

108 The fluorescence decays of all five peptides and Rev M9 delt

109 Analysis of the fluorescence decays of DNA-EB quenched by Cu(2+) and Ni(

110 In this paper, the best model for the fluorescence decays of solute molecules is selected with

111 The fluorescence decay parameters also correlated with the c

112 ing microscopy (FLIM) of NAD(P)H and FAD, so fluorescence decay parameters and the optical redox rati

113 quantifying cellular metabolism by measuring fluorescence decay parameters of endogenous fluorophores

114 s demonstrated that changes in the ultrafast fluorescence decay parameters of the bilirubin are sensi

115 The analysis of fluorescence decay poses a challenging problem for the c

116 Rather, heterogeneity in fluorescence decay processes was accommodated by the bre

117 Fluorescence decay profiles were obtained showing a mono

118 e model should display the same trend as the fluorescence decay profiles when an experimental conditi

119 cavity, we demonstrate an enhancement of the fluorescence decay rate by a factor of F = 6.89.

120 Fluorescence decay rate for the low concentration condit

121 Fluoro-Gold between 720 and 990 nm, and its fluorescence decay rate in aqueous solution and murine b

122 red with GCaMP-s and jRGECO1a-type GECI: the fluorescence decay rate of f-RCaMP1 was 21 s(-1), compar

123 ples at the molecular level by measuring the fluorescence decay rate of fluorescent probes.

124 roscopy furnishes radiative and nonradiative fluorescence decay rates in various solvent polarities.

125 n earlier image), fluorescence decay curves, fluorescence decay rates, and histograms of estimated te

126 these states do not directly impact NAD(P)H fluorescence decay rates.

127 otected from such surface quenching, and its fluorescence decay reflects reacidification kinetics.

128 Analysis of the fluorescence decay resolved two lifetimes, corresponding

129 Fluorescence decay signals from PSII reconstituted with

130 nt and incompetent states that have distinct fluorescence decay signatures indicating different base

131 t is based on deep learning (DL) to quantify fluorescence decays simultaneously over a whole image an

132 The fluorescence decay spanned a full three orders of magnit

133 Changes in the fluorescence decay suggest that FAD can exist in four co

134 of oxygen from solution lowered the rate of fluorescence decay, suggesting strategies that can be em

135 The apparent half-time for fluorescence decay (t(1/2)) in PSII(-Mn) increased from

136 asor approach is a transformation of complex fluorescence decays that does not use fits to model deca

137 to screen the different membrane phases via fluorescence decay time analysis, making this new probe

138 n solution and in gas phase by measuring the fluorescence decay time and ion-neutral collision cross

139 2AP does not exhibit the long fluorescence decay time characteristic of the free nucle

140 The absorption spectrum and fluorescence decay time components of the complex at roo

141 d emission spectra (TRES) indicate that this fluorescence decay time should be ascribed to a highly q

142 ervations: the scaling of the characteristic fluorescence decay time with the vesicle diameter and th

143 roperties, such as high solubility and short fluorescence decay time, could be obtained from fluoroph

144 cifically, we use the difference between the fluorescence decay times of fluorescently tagged antibod

145 Nonlinear fitting of the fluorescence decay times provides activation parameters

146 of different complexes led to variations in fluorescence decay times.

147 o for 15 ms to 1000 s and then to follow the fluorescence decay upon chemical dilution into excess ac

148 ain, we simultaneously record the time-lapse fluorescence decay upon pulsed laser excitation within a

149 The initial, fast fluorescence decay was assigned to DC6C dissociation fro

150 bit low fluorescence quantum yields, and the fluorescence decay was studied in different solvents, hi

151 However, the identical fluorescence decay waveforms for saturating amounts of d

152 Kinetic circular dichroism and fluorescence decays were measured simultaneously to moni

153 he electron donor, measured by time-resolved fluorescence decay, were positively correlated with the

154 analysis of simulated I(VV)(t) and I(VH)(t) fluorescence decays which were found to match perfectly

155 at AppAwt and Y21F mutant protein exhibits a fluorescence decay with a lifetime of 0.6 ns.

156 ior to data collection shows monoexponential fluorescence decay with a lifetime of 1.0 ns.

157 ted AppAwt but not Y21F also exhibits slower fluorescence decay with a lifetime of 1.7 ns.

158 Trp fluorescence decay with the onset of solvation dynamics

159 yields of 0.04-0.24, and triple exponential fluorescence decays with lifetimes of 4.4-6.6, 1.4-3.2,

160 its a respectable quantum yield and a simple fluorescence decay, with marginal amounts of dark specie