ライフサイエンスコーパス: photoconversion

1 n of the early events that drive phytochrome photoconversion.

2 ng as a crucial transient proton sink during photoconversion.

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

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

5 4.0 +/- 0.1 ns irrespective of the extent of photoconversion.

6 ease in polymer density and efficiency of PC photoconversion.

7 e possible as fresh mEosFP is produced after photoconversion.

8 events such as reversible photobleaching and photoconversion.

9 the primary motion of the chromophore during photoconversion.

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

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

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

13 bly promote the proton exchange cycle during photoconversion.

14 ergo concerted conformational changes during photoconversion.

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

16 of the chromophore and binding pocket during photoconversion.

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

18 ng domains and the PHY domain that modulates photoconversion.

19 -to-far-red light-absorbing (Pfr) reversible photoconversion.

20 sor, whereby thermal reversion competes with photoconversion.

21 ambient conditions, enabling high-efficiency photoconversion.

22 tially confined nanoreactors for solar CO(2) photoconversion.

23 luorescence emission maxima before and after photoconversion.

24 ed multiplex clonal analysis and single-cell photoconversion.

25 , chromophore ligation, and full, reversible photoconversion.

26 nP)/carbon nanotube (CNT) hybrids for energy photoconversion.

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

28 es a snapshot of synapses active just before photoconversion.

29 the HK domains are significantly altered by photoconversion.

30 uous-wave illumination results in pronounced photoconversion.

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

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

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

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

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

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

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

38 FM1-43 photoconversion analysis further reveals that small clea

39 d from the small intestine immediately after photoconversion and 2 days later.

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

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

42 n used to enhance the performance of organic photoconversion and electrochemical devices.

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

44 Our combinatorial approach of photoconversion and genetic lineage tracing demonstrates

45 In situ photoconversion and intravital microscopy indicated that

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

47 o measure the time-integrated signal and the photoconversion and photobleaching rates of fluorescent

48 parameters by fitting a three-state model of photoconversion and photobleaching to the time course of

49 This study builds a bridge between the photoconversion and photoswitching properties of probes

50 Whereas photoconversion and red-state blinking in PCFPs have bee

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

52 onvertible proteins, allowing strategies for photoconversion and spectral multiplexed applications.

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

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

55 1 s) microwave-assisted fixation followed by photoconversion and ultrastructural 3D analysis, we trac

56 FM1-43 photoconversion and ultrastructural analysis confirmed t

57 systems, providing stable and bidirectional photoconversions and tissue-compatible characteristics.

58 cations for on-surface synthesis, catalysis, photoconversion, and applications in molecular electroni

59 This review examines spectral tuning, photoconversion, and photobiology of CBCRs and recent de

60 86Ala substitutions do not affect stability, photoconversion, and spectral properties of the photorec

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

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

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

64 Using a photoconversion approach to track neutrophils within dev

65 Unlike previously reported cellular photoconversion approaches, this method does not require

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

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

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

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

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

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

72 Using photoconversion-based fate mapping and live cell trackin

73 We developed PIC-IT, a photoconversion-based isolation technique allowing effic

74 Photoconversion-based tracking revealed that liver-resid

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

76 n-to-red chromophores with similar sulfoxide photoconversion behavior compared to the anthracene anal

77 sequence identity, they demonstrate distinct photoconversion behaviors.

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

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

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

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

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

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

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

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

86 with phycocyanobilin that permits reversible photoconversion between the blue light-absorbing Pb and

87 Photoconversion between the Pr and Pfr forms facilitates

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

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

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

91 Photoconversion between these states is initiated by lig

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

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

94 ye generated from PaX(560) through traceless photoconversion bound QacR and reduced its repressor fun

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

96 For example, photoconversion cell-lineage tracing identified migrator

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

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

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

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

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

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

103 netics can be tuned by modulating the LightR photoconversion cycle.

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

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

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

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

108 have led to solar cells with extremely high photoconversion efficiencies are discussed.

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

110 However, the photoconversion efficiencies decrease with increasing pr

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

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

113 tational study of the effects of pressure on photoconversion efficiencies of perovskite solar cells (

114 The results show that the photoconversion efficiencies of PSCs increase by ~40%, f

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

116 0.15))(3) perovskite active layer achieved a photoconversion efficiency (PCE) up to 16.7%.

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

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

119 The corresponding photoconversion efficiency increases from 12.6 to 15.0%.

120 Inspired by the high photoconversion efficiency observed in natural light-har

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

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

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

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

125 Solvent polarity modifies the photoconversion efficiency suggesting charge transfer ch

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

127 rent response and a 29.9% improvement of the photoconversion efficiency was observed with the nanotub

128 More interestingly such enhancement in photoconversion efficiency was obtained when the electro

129 Apart from enhancement in photoconversion efficiency, this versatile technique pro

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

131 ell were also carried out to investigate the photoconversion efficiency.

132 al equilibrium, which limits their effective photoconversion efficiency.

133 d 410 or 460 nm) for isomerization with high photoconversion efficiency.

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

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

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

137 In this work, we used a combination of photoconversion experiments and clustered regularly inte

138 Using photobleaching and photoconversion experiments in glial cells expressing vi

139 Photoconversion experiments revealed defective transloca

140 Pulse-chase photoconversion experiments show that molecules can diff

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

142 analysis of large-scale electron tomography, photoconversion experiments, quantitative polarized ligh

143 of DRONPA and Dendra2 in photoactivation and photoconversion experiments.

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

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

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

147 Reversible photoconversion from dIbR600 to the pink membrane (dIbR4

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

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

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

151 The structural dynamics underlying Pfr-to-Pr photoconversion in a liquid solution phase are not well

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

153 Photoconversion in combination with FM dyes allows clari

154 rapped deprotonated chromophores en route to photoconversion in pH 7.9 buffer.

155 Photoconversion in planar-heterojunction organic photovo

156 Solar photoconversion in semiconductors is driven by charge se

157 reorientation of Trp496 during the Pr-to-Pg photoconversion in solution is not associated with a maj

158 estigated the role of this amino acid during photoconversion in solution using engineered protein var

159 e their stability against photobleaching and photoconversion in the context of other fluorophores usi

160 t the phenomenon of near-infrared to far-red photoconversion in the miRFP family of near infrared flu

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

162 analyzed KikR(+) immune cells (2 days after photoconversion) in peripheral lymphoid organs, meninges

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

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

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

166 , once induced by green light; yet, complete photoconversion into each SO(2)-isomeric state is rarely

167 ed the .OH and .O(2)(-) levels, promoting OP photoconversion into Pi and algae growth.

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

169 We find that photoconversion is determined by the accessibility of th

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

171 This photoconversion is induced by near-infrared light throug

172 r, an early event for the phyB isoform after photoconversion is its redistribution from the cytoplasm

173 This photoconversion is much more efficient in the D227N muta

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

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

176 Using photoconversion labelling, protein tracking, and loss-of

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

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

179 At low photoconversion light levels CaMPARI offers a wide dynam

180 Photoconversion likely involves singlet-oxygen mediated

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

182 JA-2-3B'a(2-13) (SyB-Cph1) proposed a unique photoconversion mechanism involving an A-pyrrole ring ro

183 irected Photooxidation Induced Conversion, a photoconversion mechanism that we recently introduced, w

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

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

186 Photoconversion microscopy and single-molecule measureme

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

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

189 sis of vitamin D(3) that is initiated by the photoconversion of 7-dehydrocholesterol to previtamin D(

190 he N(1)-aryl group is electron-donating, the photoconversion of a cyanotriazole to a cyanoindole is e

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

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

193 Photoconversion of AtBphP2 with far-red light then gener

194 o analysis, we used Ca(2+)- and UV-dependent photoconversion of CaMPARI2 in vivo to permanently label

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

196 nt of efficient synthetic strategies for the photoconversion of colourless compounds, namely, photoca

197 protein motions for individual steps during photoconversion of Cph1.

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

199 We monitor real-time photoconversion of dark-adapted rhodopsin to opsin, deli

200 Photoconversion of Dendra2 causes a color change from gr

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

202 UV-B treatment enabled effective photoconversion of ergosterol from both fungal mycelium

203 The molecular mechanisms for the photoconversion of fluorescent proteins remain elusive o

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

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

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

207 The photoconversion of heptamethine to pentamethine cyanines

208 elongation and floral induction through the photoconversion of inactive Pr to the Pfr signalling sta

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

210 While photoconversion of interior azobenzenes was poor, the ci

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

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

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

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

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

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

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

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

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

220 Photoconversion of rhodopsin to meta I/meta II equilibri

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

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

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

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

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

226 Photoisomerization of the bilin triggers photoconversion of the CBCR input, thereby modulating th

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

228 Concomitant with photoconversion of the flavin, an unusually long-lived t

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

230 Photoconversion of the M intermediate provides a possibl

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

232 Photoconversion of the plant photoreceptor phytochrome A

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

234 Here, we used the photoconversion of the tumor immune cell compartment to

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

236 Photoconversion of vesicles rendered fluorescent with th

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

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

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

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

241 Photoconversion, photobleaching, immunofluorescence and

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

243 Importantly, the photoconversion process is performed in situ, supporting

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

245 Singlet fission is a photoconversion process that generates a doubly excited,

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

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

248 after irradiation with blue light, detected photoconversion product(s) based on F(obs) - F(obs) diff

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

250 hyde fixation makes the fluorescence signal, photoconversion rate, and photobleaching rate of mEos3.2

251 is enabled by a recently discovered cyanine photoconversion reaction that leads to the two-carbon tr

252 The photoconversion regulates the activity of an enzymatic d

253 The substitution patterns providing the photoconversion-resistant triarylmethane fluorophores ha

254 Live imaging and photoconversion reveal impaired neutrophil reverse migra

255 In vivo photoconversion reveals that Merkel cells undergo steady

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

257 are beneficial in minimizing energy loss in photoconversion schemes.

258 ectrochemical energy conversion and storage, photoconversion, sensors, and corrosion, just to name a

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

260 well-defined linear expansions during 100 % photoconversion, suggesting that this class of solid-sta

261 The presented CD-based biomass photoconversion system opens new avenues for sustainable

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

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

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

265 s from both photosynthetic and semiconductor photoconversion systems.

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

267 Using a photoconversion technique, we found that disk membranes

268 protein (KikR) was higher immediately after photoconversion than 2 days later, indicating cell egres

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

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

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

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

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

274 We also leverage this far-red photoconversion to demonstrate UV-free photoactivated lo

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

276 article tracking, fluorescence recovery, and photoconversion to examine IRE1 clustering quantitativel

277 05 cm-1 in Pr shift to 829 and 847 cm-1 upon photoconversion to lumi-R and are replaced by a very int

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

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

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

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

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

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

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

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

286 roteins by red or far-red light promotes the photoconversion to their far-red light-absorbing Pfr sta

287 High-resolution microscopy and photoconversion tracing experiments uncover hematopoieti

288 Indirect photoconversion via the primary intermediate, bathorhodo

289 sing frontier of packing-triggered selective photoconversions via supramolecular engineering.

290 CaMPARI2 photoconversion was correlated with immediate early gene

291 Unexpectedly, photoconversion was observed in the monomer despite the

292 Local photoconversion was used to obtain the timescale of diff

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

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

295 ne AZ Cac abundance, intravital FRAP and Cac photoconversion were used to separately measure delivery

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

297 hore could increase the photoswitching-aided photoconversion while reducing trapped species.

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

299 The Z-E photoconversion yields of CH(2)CH(2)- and CH(2)S-bridged

300 1)H NMR studies show high photostability and photoconversion yields.