ライフサイエンスコーパス: photoactive

1 alyst employed in photocatalysis is, itself, photoactive.

2 -cis retinal in a 70:30 ratio which are both photoactive.

3 The food-grade TiO2 was solar photoactive.

4 and many could even be considered to be more photoactive.

5 Corresponding photoactive 2-nitrobenzyl chromophore plays a distinct r

6 xhibits stable photoluminescence and remains photoactive after continuous irradiation exceeding 2 mon

7 procedure that treats pheresed blood with a photoactive agent, received US Food and Drug Administrat

8 of polycations, enzymes, nanomaterials, and photoactive agents are being investigated.

9 ysis revealed a triplet excited state in the photoactive aggregates with a sufficiently long lifetime

10 pansion to site-specifically incorporate the photoactive amino acid p-azido-l-phenylalanine (azF) int

11 meta-Azi-propofol (AziPm) is a photoactive analog of the general anesthetic propofol.

12 To investigate the mechanism of action, a photoactive analogue, 1-azidoanthracene, was synthesized

13 The K12Ga4L6 supramolecular cage is photoactive and enables an unprecedented photoreaction n

14 nopy were characterised by tradeoffs between photoactive and non-photoactive biosynthetic pathways.

15 r multi-level structures out of a variety of photoactive and non-photoactive materials.

16 ol-8 and displayed severe losses of both non-photoactive and photoactive plastoquinone-9, resulting i

17 Moreover, the studied samples were highly photoactive and the quantum yields for the generation of

18 ocrystalline pseudopolymorph was shown to be photoactive, and it was analyzed by powder X-ray diffrac

19 The Pt-acetylide segments are electro- and photoactive, and they serve as conduits for transport of

20 of CdSeS QDs of varying band gap within the photoactive anode of a QD solar cell (QDSC).

21 -disubstituted naphthalene ring features two photoactive anthracene end-capped side arms with central

22 receptors, which incorporate two end-capped photoactive anthracene rings, being the central core an

23 Finally, we demonstrate the application of photoactive antibodies in delivering fluorophores to EGF

24 Here, we have developed photoactive antibody fragments by genetic site-specific

25 yads reported here represent a novel type of photoactive arrays with various modes of electronic inte

26 Here, the photoactive arylcobalamin EtPhCbl and the remarkably pho

27 stems, making these materials of interest as photoactive assemblies for artificial photosynthesis and

28 o capture light-induced structural events in photoactive AtUVR8 crystals.

29 WC-21, a sigma-2 ligand containing both a photoactive azide moiety and a fluorescein isothiocyanat

30 -I-14,15-EE8ZE-APSA), an EET analogue with a photoactive azido group.

31 ranes (PM) as the transducer, which contains photoactive bacteriorhodopsin, is here first demonstrate

32 theoretically and experimentally, the unique photoactive behavior of pristine and defected indium oxi

33 This complex is photoactive below 20 K, undergoing a photoinduced LS to

34 erned polyacrylamide gel that incorporates a photoactive benzophenone methacrylamide monomer.

35 ent antibody immobilization realized using a photoactive benzophenone methacrylamide polyacrylamide g

36 al of light-induced protein degradation with photoactive bifunctional molecules are discussed.

37 general and directly applies to even larger photoactive biomolecular complexes.

38 herence plays any biofunctional role in real photoactive biomolecular complexes.

39 sed by tradeoffs between photoactive and non-photoactive biosynthetic pathways.

40 e report the successful incorporation of the photoactive bis(4'-(4-carboxyphenyl)-terpyridine)rutheni

41 lyse organic solar cells with four different photoactive blends exhibiting differing dependencies of

42 hotochromic compounds which use a variety of photoactive building blocks, e.g., diarylethene, azobenz

43 mble new structures with the use of suitable photoactive building blocks.

44 One involves a photoactive carotenoid protein that decreases the transf

45 ion of energy can also be included by adding photoactive, catalytically active, or redox-active recog

46 pot reactions containing (89)Zr-oxalate, the photoactive chelate desferrioxamine B (DFO)-aryl azide (

47 The utility of these new photoactive chiral organocatalysts is then demonstrated

48 perylenediimide (PDI) different electro- and photoactive chromophores to achieve new AzaBenzannulated

49 The resulting photoactive CO-releasing polymer (photoCORP-1) incorpora

50 This photoactive CO-releasing polymer could find use in deliv

51 Polynuclear photoactive complexes are therefore very attractive, and

52 ting developments in the area of mononuclear photoactive complexes with Earth-abundant metal ions (Cu

53 mposite is reported to serve as an effective photoactive component with enhanced light-absorbing capa

54 soindigo-COF:fullerene heterojunction as the photoactive component, we realized the first COF-based U

55 C system to oxidize NO gas by using parallel photoactive composites (TiO(2) nanoribbons-carbon nanotu

56 To this end, we use the photoactive compound 2-nitrobenzaldehyde, which releases

57 in the photopolymerization processes is the photoactive compound that absorbs the light, generating

58 The nsPCR is initiated using a photoactive compound, 2-nitrobenzaldehyde (NBA), and is

59 ion-exchange reaction upon activation of the photoactive compound.

60 on of energy and charge transfer in numerous photoactive compounds and complexes.

61 f encouraging the wider application of these photoactive compounds in the photopolymerization area an

62 an also be applied to the synthesis of other photoactive compounds such as spiropyrans or spirooxazin

63 A series of novel electroactive and photoactive conjugated copolymers based on N-alkyl dithi

64 The R2lox cofactor is photoactive, converting into a second form (R2loxPhoto)

65 n the geometry of the connection between the photoactive core and the malonate moieties.

66 eps: (i) it allows for fast tethering of the photoactive core to the unsaturated pendants, especially

67 We incorporated photoactive crosslinkers into AMPA receptors using genet

68 ortant for future design of high-performance photoactive devices based on WSe(2) monolayers.

69 The photoactive diazirine 4, a potent SIRT2 inhibitor, was s

70 Here we report a series of photoactive diphenyltellurophene compounds bearing elect

71 water solubilty and the localization of the photoactive drug in bacteria.

72 review we illustrate how the interaction of photoactive drugs/potential drugs with proteins or DNA i

73 hat minium is a p-type semiconductor that is photoactive during illumination and becomes inactive in

74 We present a few selected examples of photoactive dyads and triads containing organic moieties

75 9 in EGFR-positive cells pre-loaded with the photoactive dye BPD.

76 excitation of substrates either by forming a photoactive electron donor-acceptor complex or by direct

77 to a glassy carbon electrode and used as the photoactive element to fabricate a label-free photoelect

78 s results from the exquisite organization of photoactive elements that promote rapid movement of char

79 ant rhodium-carbonyl complex was found to be photoactive, enabling the activation of benzene and form

80 et ligand-to-metal charge transfer ((2)LMCT) photoactive excited state exhibits donor-dependent charg

81 demonstrate the potential application of our photoactive films in light-driven locomotion and self-cl

82 ly transparent electrodes (OTE/SnO2) produce photoactive films that exhibit photoelectrochemical acti

83 the structural features to securely bind the photoactive flavin cofactor.

84 dynamics of the BLUF domain found in several photoactive flavoproteins, which is responsible for ligh

85 Photoactive fullerene aggregates had weaker fullerene-fu

86 se of pyridinium-activated primary amines as photoactive functional groups for deaminative generation

87 The most widely used classes of photoactive functionalities include aryl azides, diazoca

88 erophores, such as pyoverdines, which bear a photoactive group.

89 leavable linkage is held in proximity to the photoactive group.

90 gonist gabazine and incorporate a variety of photoactive groups.

91 long-time and low-frequency phenomena in the photoactive halide perovskites that are presently in the

92 nor-acceptor-acceptor' dipolar donors in the photoactive heterojunctions.

93 ere consistent with size-based theory in the photoactive hydrogels, but exceed those in unmodified po

94 homodimeric type-I RCs, the isolated RC was photoactive in the presence of oxygen.

95 y synthetic developments based on the use of photoactive iron and cobalt complexes are also covered.

96 e organic semiconductor, its addition to the photoactive layer also effectively passivates perovskite

97 olar cells (PSCs) as interlayers between the photoactive layer and Ag cathode.

98 escence allows contactless evaluation of the photoactive layer and can be used to predict the optimiz

99 find that this capping layer stabilizes the photoactive layer by changing the surface chemistry and

100 inorganic hybrid perovskites (OIHPs) are new photoactive layer candidates for lightweight and flexibl

101 ative self-absorption and re-emission by the photoactive layer itself, has been speculated to contrib

102 hermal annealing is known to enhance the BHJ photoactive layer morphology and performance.

103 The photoactive layer of bulk heterojunction solar cell, who

104 of the donor and acceptor domains within the photoactive layer of the cell.

105 g dependencies of short-circuit current upon photoactive layer thickness.

106 kite CsPb(0.5) Sn(0.5) I(3) is chosen as the photoactive layer with comprehensive bandgap and film en

107 otocurrent density are retained, whereas the photoactive layer without passivation lost its activity

108 mplementation of organic semiconductors as a photoactive layer would open up a multitude of applicati

109 83 Cs0.17 Pb(I0.6 Br0.4 )3 perovskite as the photoactive layer, glass-glass laminated devices are rep

110 identified to promote the performance of the photoactive layer.

111 cture and complex film morphology within the photoactive layer.

112 methyl ester (PC(71)BM) were chosen for the photoactive layer.

113 The optimized photoactive layers exhibit well-balanced exciton dissoci

114 -Pn) were studied for their potential use as photoactive layers in organic photovoltaic (OPV) devices

115 ight and dry air the mp-Al2 O3 /CH3 NH3 PbI3 photoactive layers rapidly decompose yielding methylamin

116 Our work suggests that selecting organic photoactive layers with a narrow distribution of tail st

117 silica electro-deoxidation, the formation of photoactive layers, silicon electrorefining, and the syn

118 e stability of CH3 NH3 PbI3 perovskite-based photoactive layers.

119 cal (PEC) sensor was designed based on ideal photoactive lead sulfoiodide (Pb(5)S(2)I(6)) as low band

120 nder blue-light irradiation and catalyzed by photoactive Lewis basic molecules such as acridine orang

121 se transition alters the conformation of the photoactive ligand in the PCP, and thereby the positions

122 silsesquioxanes by functionalizing them with photoactive ligands have made these compounds attractive

123 ave potential toxicity pathways that are not photoactive like TiO2 phases, but instead seem to be bio

124 we show that soft microrobots consisting of photoactive liquid-crystal elastomers can be driven by s

125 ly designed 12 fusions between the naturally photoactive LOV2 domain from Avena sativa phototropin 1

126 bly of gold nanorods (NRs) end-tethered with photoactive macromolecular tethers.

127 A photoactive manganese nitrosyl, namely [Mn(PaPy(3))(NO)]

128 nd design is a very effective way to isolate photoactive manganese nitrosyls that could be used to de

129 , and optical properties toward an efficient photoactive material for catalysis.

130 s the promise of TPAPC-COF as a new class of photoactive material for efficient singlet-oxygen genera

131 We developed a new photoactive material that reduces recombination by physi

132 ectrode coverage with the nanotube arrays as photoactive material was only a fraction (~10%) of that

133 been implemented that use multiple types of photoactive materials and electron mediators.

134 M = Zn and H(2)) serving as light-absorbing photoactive materials are utilized.

135 s different approaches towards protection of photoactive materials based on triplet excited state ens

136 Photoactive materials by blending a semiconductive conju

137 hasis to the nonlinear optical properties of photoactive materials for the function of optical power

138 Exclusive recycling of the photoactive materials from solar cells paves a path for

139 lthough a range of covalent azobenzene-based photoactive materials has been demonstrated, the use of

140 ethod for suspending nanoparticles and other photoactive materials in Nafion for transient spectrosco

141 A new route for fabrication of photoactive materials in organic-inorganic hybrid solar

142 The major effort to develop photoactive materials is numerously focused on the p-typ

143 dance in the use of these carbon nitrides as photoactive materials or coordination supports for metal

144 one of the greatest challenges in evaluating photoactive materials used in photovoltaic cells.

145 s, an emerging class of solution processable photoactive materials, welcome a new member with a one-d

146 udies will help guide the development of new photoactive materials.

147 tes with advantages offered by both types of photoactive materials.

148 ures out of a variety of photoactive and non-photoactive materials.

149 cs remains a critical goal for understanding photoactive materials.

150 electrons and nuclei govern the function of photoactive materials.

151 lymers (CPs) have emerged as novel promising photoactive materials.

152 maticity and insight to designing functional photoactive materials.

153 he use of a chemical oxidant such as Ce(4+), photoactive mediators such as [Ru(bpy)3](2+), or electro

154 Although these substrates contain photoactive metal oxides, little is known about the role

155 none amino acid (Naq) with histidine-ligated photoactive metal-tetrapyrrole cofactors, creating a 100

156 from scavenging photogenerated holes to the photoactive modified electrode.

157 The photoactive MOFs act as an excellent light-harvesting sy

158 zation scaffold for IEF-focused proteins via photoactive moieties.

159 togenetics, super-resolution microscopy, and photoactive molecular devices.

160 can be obtained by in situ encapsulation of photoactive molecules (sulfonated spiropyran, SSP), as t

161 Light-driven degradation of photoactive molecules could be one of the major obstacle

162 his UV range can be used in conjunction with photoactive molecules for photo-reconfiguration, while a

163 ed singlet oxygen is highly reactive, so the photoactive molecules in the system are quickly oxidized

164 devoted to the synthesis and utilization of photoactive molecules that are able to generate a base o

165 ride (g-C3N4) and titanium dioxide (TiO2) as photoactive nanomaterials, ascorbic acid (AA) as electro

166 vskite to percolate and form a complementary photoactive network.

167 Here, we used a photoactive nucleotide, 4-thioU, to study the interactio

168 th OCP apoprotein, resulting in formation of photoactive OCP from completely photoinactive species.

169 thylrhodamine-maleimide (TMR) and obtained a photoactive OCP-TMR complex, the fluorescence of which w

170 e, we expand the range of such structures to photoactive ones by using semiconducting transition meta

171 rent polymers that are either pH=responsive, photoactive or biodegradable can be used to form the hyd

172 In cyanobacteria, the photoactive Orange Carotenoid Protein (OCP) and the Fluo

173 The photoactive orange carotenoid protein (OCP) is essential

174 The photoactive Orange Carotenoid Protein (OCP) is involved

175 The photoactive Orange Carotenoid Protein (OCP) photoprotect

176 This mechanism is triggered by the photoactive Orange Carotenoid Protein (OCP), which acts

177 on that occurs upon energy transfer from the photoactive organic antennas to the lanthanide species.

178 inorganic-organic solar absorber based on a photoactive organic cation.

179 chnologies for photo-regulated release using photoactive organic materials that directly absorb visib

180 the cyclic peptide Gramicidin S (GS) and the photoactive organonometallic complex ruthenium tris-bipy

181 These bacteria form a mat-like photoactive outer layer around an otherwise unconsolidat

182 and frequency of prolamellar bodies, and in photoactive Pchlide conversion.

183 tral and hydrophobic porphyrin, which is not photoactive per se against Gram-negative bacteria, effic

184 Photoactive perovskite semiconductors combine effective

185 Pseudomonas aeruginosa with an intact, fully photoactive photosensory core domain in its dark-adapted

186 er, have identified a plastidial pool of non-photoactive phylloquinone that could be involved in addi

187 ed severe losses of both non-photoactive and photoactive plastoquinone-9, resulting in near complete

188 this suggests that the high potency of such photoactive platinum complexes is related to their dual

189 A microscope slide supporting a 30-mum-thick photoactive polyacrylamide gel enables western blotting:

190 we scrutinize solute interactions with a UV photoactive polyacrylamide gel that incorporates a benzo

191 The 3D microfluidic device is a photoactive polyacrylamide gel with a microwell array-pa

192 A new photoactive polymer comprising benzo[1,2-b:3,4-b':5,6-d'

193 on into liquid-crystal networks, we generate photoactive polymer films that exhibit continuous, direc

194 ted that the incorporation of the conjugated photoactive polymer into organolead halide perovskites d

195 A novel photoactive polymer with two different molecular weights

196 ating trap-embedded components from pristine photoactive polymers based on the unimodality of molecul

197 omposed of monolithic inorganic materials or photoactive polymers.

198 l-8 originates from a subfraction of the non-photoactive pool of plastoquinone-9.

199 ss of plastoquinone-9, restricted to the non-photoactive pool, was sufficient to eliminate half of th

200 ith streptavidin-coated magnetic beads and a photoactive porphyrin complex.

201 s the design, properties, and application of photoactive probes used to study amyloid aggregation, as

202 The produced NP bridges were found to be photoactive, producing photocurrent upon illumination.

203 onductive polymers and halide perovskites in photoactive properties enables to create various combina

204 clarify the dependence of Se content on the photoactive properties of CdTexSe1-x alloy layers in ban

205 The photoactive properties of COK-69 were investigated in de

206 lly encoded structural designs incorporate a photoactive protein domain to enable light-dependent con

207 ) is a structurally and functionally modular photoactive protein involved in cyanobacterial photoprot

208 carotenoid protein (OCP) is a water-soluble, photoactive protein involved in thermal dissipation of e

209 low-frequency terahertz spectroscopy of two photoactive protein systems, rhodopsin and bacteriorhodo

210 Orange carotenoid protein (OCP) is the photoactive protein that is responsible for high light t

211 nge carotenoid protein (OCP) is a two-domain photoactive protein that noncovalently binds an echineno

212 To understand how photoactive proteins function, it is necessary to unders

213 Recently, photoactive proteins have gained a lot of attention due

214 and sensory rhodopsin II (SRII), homologous photoactive proteins in haloarchaea, have different mole

215 the design elements required to generate new photoactive proteins with novel function.

216 s approach can be generally applied to other photoactive proteins.

217 odel system for the study of this process in photoactive proteins.

218 All substitutions yield a folded, photoactive PYP, illustrating the robustness of protein

219 ptor 2, bearing two urea arms decorated with photoactive pyrenyl rings, acts as a highly selective fl

220 ctase (RNR) as compared to tyrosine-modified photoactive Re(I) and Ru(II) complexes].

221 channels allows rapid and uniform supply of photoactive reagents by a convection-diffusion mechanism

222 Phytochromes are well-known as photoactive red- and near IR-absorbing chromoproteins wi

223 MSH1 depletion alters non-photoactive redox behavior in plastids and a sub-set of

224 st to conventional studies that extract bR's photoactive retinal along with the first transmembrane h

225 Proton-pumping rhodopsins (PPRs) are photoactive retinal-binding proteins that transport ions

226 the ion path is blocked mid-membrane by its photoactive retinylidene chromophore and further by a cy

227 of its dark (closed) state revealed that the photoactive retinylidene chromophore is located midmembr

228 Proteorhodopsins (PRs), photoactive retinylidene membrane proteins ubiquitous in

229 Microbial rhodopsins are a family of photoactive retinylidene proteins widespread throughout

230 anic frameworks (MOFs) were synthesized from photoactive Ru(II)-bpy building blocks with strong visib

231 an anionic Zr-MOF which selectively uptakes photoactive [Ru(bpy)3](2+) for heterogeneous photo-oxida

232 The system consists of a photoactive Ruthenium complex capable of inducing a chan

233 borazine-azobenzene derivative, we used this photoactive scaffold to engineer soluble BN-doped polyth

234 The functionality of a photoactive semiconductor (i.e., photocatalysts, photoel

235 This challenging process requires photoactive semiconductors enabling solar energy driven

236 c frameworks (COFs) are an emerging class of photoactive semiconductors, tunable at a molecular level

237 th Ala or Glu perturbed the structure of the photoactive site and resulted in significantly shifted v

238 ion of spectral shifts in the mutants of the photoactive site carboxylic acid residues.

239 The structure also reveals a novel photoactive site configuration that maintains the retiny

240 e that the local electrical field across the photoactive site controls fast and slow channel closing,

241 In prior studies, differences in the photoactive site defined the two forms, namely the direc

242 dopsin I distinguished by differences in its photoactive site have been shown to be directly correlat

243 Our data provide novel insight into the photoactive site of channelrhodopsin-2 during the photoc

244 absence of ATP introduce flexibility to the photoactive site prior to FAD excitation, with the conse

245 hree main conclusions regarding the roles of photoactive site residues in signaling emerge from the c

246 as acceptor and donor, respectively, of the photoactive site Schiff base (SB) proton.

247 n of the retinylidene Schiff base in the SRI photoactive site to inner or outer half-channels.

248 uctural changes in helix F, distant from the photoactive site, correspond to the opposite phototaxis

249 istry is likely to be introduced into the BR photoactive site.

250 the distance of the mutated residue from the photoactive site.

251 Another photoactive-site residue corresponding to Asp(212) in ba

252 ater salt constituents (e.g., carbonates) or photoactive species (e.g., iron and nitrate).

253 f AgCl((aq)), suggesting that it is the most photoactive species in those systems.

254 ive decay, (1) and too short-lived to be the photoactive species.

255 s on silica nanoparticles, were printed on a photoactive surface followed by covalent immobilization

256 Highly photoactive, tetrahedral Ti4+ sites can be created, othe

257 s, yet nC70 appears to be significantly more photoactive than nC60.

258 ibution and density and increase the maximal photoactive thickness for efficient operation.

259 Photoactive TiO(2) served to convert incident photons in

260 the vdW p-g-n junctions containing multiple photoactive TMDs can provide a viable approach toward fu

261 )phosphine] is both strongly luminescent and photoactive toward carbon monoxide release.

262 icating that the dual-action complex is more photoactive toward cells in spite of its low ligand exch

263 with molecular iodine, as well as the use of photoactive transition metal carbonyls in the presence o

264 Microbial rhodopsins are a diverse group of photoactive transmembrane proteins found in all three do

265 A series of photoactive triads have been synthesized and investigate

266 ntly shifts the overall equilibrium toward a photoactive tricomponent species.

267 The electrode was found to be photoactive under both visible light and UV-vis irradiat

268 systems, the best performing polymer is only photoactive under visible rather than ultraviolet irradi

269 Both OCP1 and OCP2 heterodimers are photoactive, undergoing light-driven heterodimer dissoci

270 emical experiments show that the material is photoactive with p-type conductivity.

271 of hydroxylated products that were no longer photoactive, with primary photoproducts consisting of mo

272 We used microcrystals of photoactive yellow protein (a bacterial blue light photo

273 para-coumaric acid - a model chromophore for photoactive yellow protein (PYP) - leads to a bifurcatio

274 ng the photoexcitation of the R52Q mutant of photoactive yellow protein (PYP) are investigated, for t

275 e apply this strategy to a set of mutants of photoactive yellow protein (PYP) containing all 20 side

276 me using neutron diffraction techniques on a photoactive yellow protein (PYP) crystal in a study publ

277 bility to track the reversible photocycle of photoactive yellow protein (PYP) following trans-to-cis

278 Photoactive yellow protein (PYP) is a prototypical signa

279 Photoactive yellow protein (PYP) is a signaling protein

280 at the residual structure in fully denatured photoactive yellow protein (PYP) is affected by isomeriz

281 The 14 kDa soluble cytosolic photoactive yellow protein (PYP) is believed to be the p

282 The nature of the optical cycle of photoactive yellow protein (PYP) makes its elucidation c

283 Distinct conformational changes of single photoactive yellow protein (PYP) molecules were captured

284 The signaling state of the photoactive yellow protein (PYP) photoreceptor is transi

285 The active site of photoactive yellow protein (PYP) provides a model system

286 Herein, we use photoactive yellow protein (PYP) to measure the first ex

287 e picosecond time range in the photocycle of photoactive yellow protein (PYP) with MHz X-ray pulse ra

288 We test this prediction using photoactive yellow protein (PYP), a 125-residue prototyp

289 ponsible for this response is believed to be photoactive yellow protein (PYP), whose chromophore phot

290 of a low-barrier hydrogen bond (LBHB) in the photoactive yellow protein (PYP).

291 dshift in the visible absorbance spectrum of photoactive yellow protein (PYP).

292 gen-bonded cofactors in proteins such as the photoactive yellow protein (PYP).

293 active site of the bacterial photoreceptor, photoactive yellow protein (PYP).

294 t GFPs and other photosensory proteins, like photoactive yellow protein and rhodopsin, provide potent

295 Y-FAST was engineered from the 14-kDa photoactive yellow protein by directed evolution using y

296 solved serial femtosecond crystallography on photoactive yellow protein microcrystals over a time ran

297 s-to-cis isomerization of the chromophore in photoactive yellow protein.

298 f an isolated model chromophore anion of the photoactive yellow protein.

299 crystallographic data for the photocycle of photoactive yellow protein.

300 udies on subnanosecond events in rhodopsins, photoactive yellow proteins, phytochromes, and some othe