ライフサイエンスコーパス: photoconversion

1 e possible as fresh mEosFP is produced after photoconversion.

2 events such as reversible photobleaching and photoconversion.

3 the primary motion of the chromophore during photoconversion.

4 , as in a screen of 12 proteins, 8 exhibited photoconversion.

5 conformation changes occur during Pb --> Pg photoconversion.

6 l role of the PHY domain in efficient Pr/Pfr photoconversion.

7 bly promote the proton exchange cycle during photoconversion.

8 ergo concerted conformational changes during photoconversion.

9 h respect to chromophore ligation and Pr/Pfr photoconversion.

10 of the chromophore and binding pocket during photoconversion.

11 PHY (phytochrome) domains to achieve Pr/Pfr photoconversion.

12 ng domains and the PHY domain that modulates photoconversion.

13 ges of distance distributions upon Pr-to-Pfr photoconversion.

14 the HK domains are significantly altered by photoconversion.

15 uous-wave illumination results in pronounced photoconversion.

16 ange in filaments by long-term imaging after photoconversion.

17 he network, even in cells that divided after photoconversion.

18 ng as a crucial transient proton sink during photoconversion.

19 curs in Synechococcus OS-B' phytochrome upon photoconversion.

20 ons made by ALPM nkx2.5(+) cells using Kaede photoconversion.

21 4.0 +/- 0.1 ns irrespective of the extent of photoconversion.

22 ease in polymer density and efficiency of PC photoconversion.

23 Using fluorescence loss after photoconversion, a novel, high-speed alternative to fluo

24 BphP3 respond to light quality by reversible photoconversion, a property that requires the light-abso

25 Full-length Tlr0924 exhibits blue/green photoconversion across a broad range of temperatures, in

26 ld, and an action spectrum for the PM-->LIBM photoconversion all indicate that the PM-->LIBM and Mon-

27 The photoconversion also results in an 18 cm-1 decrease in t

28 FM1-43 photoconversion analysis further reveals that small clea

29 progress, the detailed mechanism of the OCP photoconversion and associated photoprotection remains e

30 Specifically we use FRAP, fixation, photoconversion and correlative light and electron micro

31 contrast, Tolypothrix OCP2 shows both faster photoconversion and faster back-conversion, lack of regu

32 f the tongue is indispensable for Pr --> Pfr photoconversion and involves a swap of the motifs' trypt

33 allosteric features that inhibit or promote photoconversion and reversion of Pfr back to Pr, thus al

34 ion of the Spinach-fluorogen complex induces photoconversion and subsequently fluorogen dissociation,

35 s, undergoes significant rearrangements upon photoconversion and transits from the stable orange to t

36 1 s) microwave-assisted fixation followed by photoconversion and ultrastructural 3D analysis, we trac

37 FM1-43 photoconversion and ultrastructural analysis confirmed t

38 86Ala substitutions do not affect stability, photoconversion, and spectral properties of the photorec

39 coupled with measurements of solution size, photoconversion, and thermal reversion, we identified bo

40 tives can be switched in both ways with high photoconversions, and their Z-isomers display a remarkab

41 iosensors, long-distance communications, and photoconversion applications.Plasmon-induced hot electro

42 l indicate that the PM-->LIBM and Mon-->CMon photoconversions are both mediated by a sequential bipho

43 he PM-->LIBM and monomer-->colorless monomer photoconversions are mediated by similar biphotonic mech

44 nd 3570 cm(-)(1) shift to 3640 cm(-)(1) upon photoconversion at 173 K.

45 uced conversion to its active form, and that photoconversion back to its inactive form causes dissoci

46 to Pfr, which can be reversed by subsequent photoconversion back to Pr.

47 ence microscopy, single-particle tracking, a photoconversion-based assay, and mathematical modeling,

48 Using photoconversion-based fate mapping and live cell trackin

49 osensory core module, which exhibits altered photoconversion behavior and different crystal packing f

50 sequence identity, they demonstrate distinct photoconversion behaviors.

51 sponses in plants and microorganisms through photoconversion between a red light-absorbing ground sta

52 ins for contrast and stability of reversible photoconversion between high- and low-fluorescent states

53 Interpreted as transient photoconversion between neutral cis and anionic trans ch

54 rbing states, whereas RpBphP3 exhibits novel photoconversion between Pr and a near-red (Pnr) light-ab

55 , fungi, and bacteria by means of reversible photoconversion between red (Pr) and far-red (Pfr) light

56 n plants, fungi, and bacteria via reversible photoconversion between red (Pr) and far-red (Pfr) light

57 lassical" phytochrome behavior of reversible photoconversion between red (Pr) and far-red (Pfr) light

58 They undergo reversible photoconversion between red-absorbing (Pr) and far-red-a

59 Photoconversion between the Pr and Pfr forms facilitates

60 parallel 'head-to-head' arrangement and that photoconversion between the Pr and Pfr forms involves co

61 lassical phenotype that undergoes reversible photoconversion between the Pr and Pfr states.

62 hromophore that undergo a typical reversible photoconversion between the two spectrally different for

63 Photoconversion between these states is initiated by lig

64 eir photocycle, which consists of reversible photoconversion between two photostates.

65 ocesses in microorganisms and plants through photoconversion between two stable states, a red light-a

66 tooxidation commonly results in green-to-red photoconversion called oxidative redding.

67 Finally, FM1-43 photoconversion combined with electron microscopy analys

68 reater brightness, faster maturation, higher photoconversion contrast and better photostability.

69 ration of the flow system provided up to 50% photoconversion contrast in-flow at a droplet rate of fe

70 hotoswitching action spectrum, 9-fold higher photoconversion contrast, and up to 10-fold faster photo

71 LY) in fixed brain slices and examined after photoconversion; corticothalamic axons and terminals wer

72 the red and green forms of mEosFP following photoconversion could be used to estimate production of

73 The rate of fluorescence recovery after photoconversion decreased with synaptic volume in both t

74 ly, genetic cell-lineage tracing using Kaede photoconversion demonstrates that de novo hair cells der

75 tobleaching, fluorescence intermittency, and photoconversion dynamics of Dendra2, a well-known PAFP u

76 All of these small molecules show high photoconversion efficiencies (PCEs), ranging from 3.18-6

77 Upon illumination, monochromatic incident photoconversion efficiencies between 1.2 and 9.3% were d

78 ce interface recombination losses to achieve photoconversion efficiencies of 6.5%.

79 ade in terms of light-harvesting and overall photoconversion efficiencies of copper(I)-containing DSC

80 The observed photoconversion efficiency (IPCE) of approximately 4% is

81 dSe quantum dots and (ii) improvement in the photoconversion efficiency by facilitating the charge tr

82 photoexcited state and how this affects the photoconversion efficiency has yet to be determined.

83 tter value compares favorably with a maximum photoconversion efficiency of 1% for n-type TiO2 biased

84 l conversion efficiency of 11% and a maximum photoconversion efficiency of 8.35% when illuminated at

85 explaining the limited photovoltage and poor photoconversion efficiency of iron pyrite single crystal

86 sassembled states, resulting in an increased photoconversion efficiency of more than 300% over 168 ho

87 o tune the photoelectrochemical response and photoconversion efficiency via size control of CdSe quan

88 ses play a pivotal role in dictating the net photoconversion efficiency.

89 potentially a limiting factor in haematite's photoconversion efficiency.

90 ed loading of the lipophilic dye FM1-43 with photoconversion, electron microscopy, and electrophysiol

91 The Pr to lumi-R photoconversion exhibits a thermal barrier and is comple

92 Using photobleaching and photoconversion experiments in glial cells expressing vi

93 Photoconversion experiments revealed defective transloca

94 Pulse-chase photoconversion experiments show that molecules can diff

95 d fluorescence recovery after photobleaching/photoconversion experiments showed that these inclusions

96 of DRONPA and Dendra2 in photoactivation and photoconversion experiments.

97 photoswitching with real-time calculation of photoconversion fluorescence contrast.

98 Here, we provide a detailed picture of photoconversion for the photosensing cGMP phosphodiester

99 otocrystallography reveals the highest known photoconversion fraction of 58(3)% (in 1) for any solid-

100 Reversible photoconversion from dIbR600 to the pink membrane (dIbR4

101 t, localized and non-invasive method for GFP photoconversion from green to red.

102 Photoconversion from Pr to Pfr is initiated by a light-d

103 imescales of the reactions involved in these photoconversions have not been conclusively shown.

104 tible and cell-permeable dye, we demonstrate photoconversion in a variety of cell lines, including de

105 Photoconversion in combination with FM dyes allows clari

106 Photoconversion in planar-heterojunction organic photovo

107 Solar photoconversion in semiconductors is driven by charge se

108 shown to be incapable of protochlorophyllide photoconversion in vivo and is thought to be defective i

109 hore locked in a deprotonated Meta-R(c)-like photoconversion intermediate after red light irradiation

110 iate diazirine 3, which undergoes subsequent photoconversion into 1-amino-3-methylcarbodiimide (H2N-N

111 Initially weakly fluorescent PAiRFPs undergo photoconversion into a highly fluorescent state with exc

112 relating color recovery of H2B::mEosFP after photoconversion is a novel approach involving a single F

113 We found that photoconversion is fairly common among orange and red fl

114 This photoconversion is much more efficient in the D227N muta

115 enic Arabidopsis plants, we demonstrate that photoconversion is not a prerequisite for phytochrome si

116 The quantum efficiency of this photoconversion is similar to rhodopsin.

117 ts to increase visual fidelity, reducing the photoconversion lag is much more important than improvin

118 otocol that will enable one to control their photoconversion levels.

119 At low photoconversion light levels CaMPARI offers a wide dynam

120 Photoconversion likely involves singlet-oxygen mediated

121 ane-bound diffusion through a combination of photoconversion, live-cell superresolution experiments,

122 ent spectra reveals exciton dissociation and photoconversion mechanisms in TMDCs.

123 opic levels by using a novel high-resolution photoconversion method based in the high affinity of pha

124 Protein conformational changes in these photoconversions monitored by site-directed spin labelin

125 y, they have been found to undergo efficient photoconversion not only by the traditional 400-nm illum

126 unusual spectral feature is associated with photoconversion of a previously unknown light-sensitive,

127 We investigate the photoconversion of aqueous 8 nm Ag nanocrystal seeds int

128 Photoconversion of AtBphP2 with far-red light then gener

129 ebrafish brain could be marked by subsequent photoconversion of co-expressed Kaede or Dendra.

130 protein motions for individual steps during photoconversion of Cph1.

131 Two-photon photoconversion of cyanine-based dyes offer several adva

132 Photoconversion of Dendra2 causes a color change from gr

133 he light microscope, and used to trigger the photoconversion of diaminobenzidine, allowing 4D optical

134 Spatially confined green-to-red photoconversion of fluorescent proteins with high-power,

135 By combining photoconversion of FM1-43-stained vesicles and electron

136 reating new transgenic lines, our method for photoconversion of GFP allows the use of existing GFP-ta

137 n the zebrafish, using computer-guided laser photoconversion of injected Kaede protein and flow cytom

138 We utilized photoconversion of intestinal cells in Kaede mice to tra

139 e found that POm stimulation triggers robust photoconversion of layer 5 cortical neurons and weaker c

140 tinal chromophore, whereas the intracircular photoconversion of M back to D involves only one C13=C14

141 degrees C) reveals two intermediates in the photoconversion of M, which we termed M' (or M'(404)) an

142 The photomagnetic effect is induced by the photoconversion of Mo(IV) ions in low spin (LS) configur

143 temperatures (77-175 K) shows the extent of photoconversion of one-electron-oxidized guanine and the

144 The contrast between the presumed photoconversion of phytochrome far red-absorbing (Pfr) t

145 ith intense 532 nm pulses by contrasting the photoconversion of PM with that of monomeric BR solubili

146 amino acids change their environment during photoconversion of Pr to Pfr, which can be reversed by s

147 Photoconversion of rhodopsin to meta I/meta II equilibri

148 projections at the central level by specific photoconversion of sensory neurons.

149 Two-photon photoconversion of single and small numbers of mKikGR-la

150 r dynamics using fluorescence recovery after photoconversion of synapses in intact zebrafish and corr

151 Taken together, photoconversion of T. elongatus PixJ from Pb to Pg invol

152 ryotrapping techniques, to follow the entire photoconversion of the blue-absorbing states to the gree

153 meric state of the dye; specifically, 30-35% photoconversion of the closed-ring spiropyran (SP) moiet

154 g7, dark reversion was so rapid that reverse photoconversion of the green-absorbing photoproduct was

155 Photoconversion of the M intermediate provides a possibl

156 Changes in the FTIR difference spectra upon photoconversion of the M intermediate to its photoproduc

157 Photoconversion of the plant photoreceptor phytochrome A

158 increases in fluorescence emission caused by photoconversion of the protein chromophore.

159 Through targeted photoconversion of UAS-driven Kaede and variegated expre

160 Photoconversion of vesicles rendered fluorescent with th

161 ring the mechanistic differences between the photoconversions of BV-type and phytobilin-type phytochr

162 neurofilament fusion proteins and then used photoconversion or photoactivation strategies to create

163 We carried out photoconversion (PC) of the fluorescent endocytotic mark

164 ations include (i) large Stokes shifts, (ii) photoconversions, photoactivation, and photoswitching, (

165 Photoconversion, photobleaching, immunofluorescence and

166 Schiff base and undergo displacement during photoconversions, presumably shuttling between the Schif

167 Here, we followed the complete green-to-blue photoconversion process of the phycoviolobilin chromopho

168 sfer in a neighbouring medium, could augment photoconversion processes, potentially leading to an ent

169 Mass spectrometry suggests that the photoconversion product is a thiol-cyanine adduct in whi

170 wo promising variants that exhibit excellent photoconversion properties and have an up to 4.6-fold in

171 eoptiles or extracts) sufficient to approach photoconversion saturation reduced phosphorylation of im

172 are beneficial in minimizing energy loss in photoconversion schemes.

173 conceptual challenges to the optimization of photoconversion since an atomic-scale description has so

174 air created via photon absorption in organic photoconversion systems must overcome the Coulomb attrac

175 that charge separation in efficient organic photoconversion systems occurs through hot-state charge

176 ults point towards new design rules both for photoconversion systems, enabling the suppression of ele

177 s from both photosynthetic and semiconductor photoconversion systems.

178 The resolution of the photoconversion technique allowed us to examine the loca

179 Using a photoconversion technique, we found that disk membranes

180 mutagenic studies support a toggle model for photoconversion that engages multiple features within th

181 nce energy transfer, we determined that upon photoconversion, the distance between TMR (donor) bound

182 6) cm(4) s molecule(-1) photon(-1)) of these photoconversions, the temporal and spectral characterist

183 Unlike other phytochromes, photoconversion thus results in a pKa shift of more than

184 ference contrast and fluorescence loss after photoconversion time-lapse microscopy.

185 tion in spines and followed by global sparse photoconversion to determine spine morphologies with nan

186 05 cm-1 in Pr shift to 829 and 847 cm-1 upon photoconversion to lumi-R and are replaced by a very int

187 reporter for optimizing and quantifying the photoconversion to metarhodopsin-I.

188 is substantially more stable in planta upon photoconversion to Pfr and is hyperactive in driving pho

189 In contrast, photoconversion to Pfr is highly sensitive to the chromo

190 inds selectively and reversibly to PIF3 upon photoconversion to Pfr, but that the apparent affinity o

191 C terminus whose activity is repressed after photoconversion to Pfr.

192 mponent kinase motif that is repressed after photoconversion to Pr.

193 eptide editing in real time after ultra-fast photoconversion to pseudoempty MHC I molecules.

194 proton acceptor from the Schiff base during photoconversion to the receptor signaling state.

195 Indirect photoconversion via the primary intermediate, bathorhodo

196 Unexpectedly, photoconversion was observed in the monomer despite the

197 Local photoconversion was used to obtain the timescale of diff

198 ger than the band edge of CdS, extending the photoconversion wavelength from 525 to 725 nm.

199 ndent measures-calibrated imaging, FRAP, and photoconversion-we find that the Dam1 submodule is uncha

200 the PIN2-Dendra2 plasma membrane pool after photoconversion when they were used in high concentratio

201 uorescent proteins specifically designed for photoconversion will usually be advantageous when creati