ライフサイエンスコーパス: light-harvesting

1 cise blue print of the regulatory network of light harvesting.

2 tallization, phase separation, and efficient light harvesting.

3 tio, in these membranes allows for efficient light harvesting.

4 ranging from gas separation to catalysis and light harvesting.

5 ctions and therefore the mechanisms used for light harvesting.

6 rocesses for directional charge transport or light harvesting.

7 organisms have discovered many solutions for light harvesting.

8 etic landscape and ensuring highly efficient light-harvesting.

9 pt that could efficiently be used to enhance light harvesting?

10 The structure of the RC/YFP-light-harvesting 1 (LH1) complex shows the position of Y

11 d monomeric and dimeric reaction center (RC)-light-harvesting 1 (LH1)-PufX "core" complexes.

12 h the genetically modified and the wild-type light harvesting 2 complexes of Rhodopseudomonas palustr

13 h is applied to the 2DES spectroscopy of the Light-Harvesting 2 (LH2) complex of purple bacteria.

14 hat controls expression of genes for the low light harvesting 4 (LH4) antenna complex.

15 ta communication, high-speed electronics and light harvesting (8-16) require a thorough understanding

16 Ancillary ligands carry favorable light-harvesting abilities and are therefore crucial in

17 ization of DSSCs due to their more favorable light-harvesting abilities and long-term thermal and che

18 further promote the exciton dissociation or light harvesting ability of these PHJs via alternative a

19 ydrogen-evolving catalyst (HEC) exhibit good light-harvesting ability and enhanced photoresponses com

20 ge of the solar spectrum, which limits their light-harvesting ability and leads to colouring of the l

21 favorable properties of the polymer, such as light-harvesting ability.

22 We also identified a transcript encoding a light harvesting AcpPC protein with homology to Chlamydo

23 d increase the photovoltage, and to improved light harvesting across the visible region.

24 , changes in internal biophysical processes, light-harvesting adaptations (e.g., variations in leaf a

25 ne PC disc per rod is sufficient for maximal light harvesting and biomass accumulation, except under

26 al (PEC) water splitting, but limitations in light harvesting and charge collection have necessitated

27 s and reduce bandgap, which is beneficial to light harvesting and enhancing short-circuit current den

28 ons that range from light-emitting diodes to light harvesting and light sensors, and to valleytronics

29 Plants must switch rapidly between light harvesting and photoprotection in response to envi

30 chemical processes that depend on plasmonic light harvesting and the transfer of nonequilibrium char

31 erstanding of the impact of heterogeneity on light harvesting and thus how these systems are optimize

32 r cells has a profound influence on both the light harvesting and TTA-UC efficiency.

33 ogical components can synergistically couple light-harvesting and catalytic functions for solar-to-ch

34 t reactions of photosynthesis, which include light-harvesting and charge separation, take place in th

35 ximide (PMI) pi-aggregates provide important light-harvesting and electron-hole pair generation advan

36 e potentially relevant to the development of light-harvesting and electron-transport devices.

37 e for the development of novel materials for light-harvesting and optoelectronic applications.

38 We assess the progress made in terms of light-harvesting and overall photoconversion efficiencie

39 actions are of fundamental importance to the light-harvesting and photoprotective functions essential

40 emistry to produce favorable arrangements of light-harvesting and redox-active chromophores in space.

41 Light-harvesting and resonance energy transfer to the ca

42 erent nanoscale energy transport, artificial light-harvesting, and nanophotonics.

43 ); light-harvesting complex II (LHCII), PSII light harvesting antenna (site); and changes in the ante

44 sunlight may result in overexcitation of the light-harvesting antenna and the formation of reactive c

45 ctivated by intense blue light, binds to the light-harvesting antenna and triggers the dissipation of

46 tailed architecture of the extant seed plant light-harvesting antenna can now be dated back to a time

47 PSI is served by both LHCII and four light-harvesting antenna complex I (LHCI) subunits, Lhca

48 The monomeric photosystem I-light-harvesting antenna complex I (PSI-LHCI) supercompl

49 edox control of the phosphorylation state of light-harvesting antenna complex II (LHCII).

50 e individual pigment chromophores present in light-harvesting antenna complexes are introduced, and t

51 ructural rearrangements of PSII and (likely) light-harvesting antenna complexes into a photochemicall

52 Light-harvesting antenna complexes not only aid in the c

53 As opposed to PSII and cytochrome f, the light-harvesting antenna complexes of PSII remain stable

54 y effects with respect to the association of light-harvesting antenna complexes to PS I.

55 n the aggregation state of the phycobilisome light-harvesting antenna components.

56 terminants required for interaction with the light-harvesting antenna during photoprotection.

57 ible proteins (Hlips) that are homologous to light-harvesting antenna of plants and algae.

58 Therefore, the light-harvesting antenna system of photosystem II in thy

59 getic effects leading to EET optimization of light-harvesting antenna systems while exploring the str

60 multichromophore system serves as a modular light-harvesting antenna that is capable of being optimi

61 o the lower temperature, the proteins of the light-harvesting antenna were greatly down-regulated and

62 ton transfer components and their associated light-harvesting antenna.

63 the phycobilisome (PB), the extramembranous light-harvesting antenna.

64 Here we show that a light-harvesting antenna/reaction centre mimic can be re

65 Energy transfer and trapping in the light harvesting antennae of purple photosynthetic bacte

66 eresting platform to hierarchically organize light-harvesting antennae and catalytic centers to achie

67 mobility reflect the different ways in which light-harvesting antennae can be regulated in mesophilic

68 ains a reaction centre that is surrounded by light-harvesting antennae, which absorb the light and tr

69 are integral for these clusters to serve as light-harvesting antennae.

70 implications for the design of bio-inspired light-harvesting antennas and the redesign of natural ph

71 P)-all rigidly linked to each other-serve as light-harvesting antennas as well as electron donors and

72 energy-transfer dynamics and pathways in the light-harvesting antennas of various photosynthetic orga

73 id in the efficient transport of energy from light-harvesting antennas to photosynthetic reaction cen

74 gulation is controlled by the association of light-harvesting antennas with accessory quenchers such

75 ce an atomistic model that mimics a complete light-harvesting apparatus of green sulfur bacteria.

76 Green-sulfur bacteria have evolved a unique light-harvesting apparatus, the chlorosome, by which it

77 portant and useful design rules for QD-based light harvesting applications using the exciton-surface

78 upconversion enhancement for biosensing and light harvesting applications.

79 These proteins are interesting for light-harvesting applications in bioenergy production, i

80 ir use in building multiporphyrin arrays for light-harvesting applications, their use as ligands to f

81 at the compounds studied may have utility in light-harvesting applications.

82 cyclic molecular systems for electronic and light-harvesting applications.

83 atory mechanisms can be applied to inorganic light-harvesting arrays displaying switchable catalytic

84 We also applied this catalyst in a light-harvesting artificial leaf platform that concurren

85 high Voc , and its ability to contribute to light harvesting at 600-800 nm.

86 Here, we model light harvesting at the several-hundred-nanometer scale

87 med into electronic excitation energy of the light-harvesting biomolecular complexes.

88 systems is precise structural control of the light-harvesting building blocks.

89 critical test for two contrasting models of light harvesting by photosystem II cores, known as the t

90 functions under NIR excitation at 800 nm: 1) Light harvesting by the UCNP shell containing Nd and sub

91 Photosynthetic light harvesting can be down-regulated by nonphotochemic

92 itivity to static disorder to increase their light-harvesting capability in a number of ways.

93 gn of PSI allows for a large increase of its light-harvesting capacities.

94 ems (PS) I and II activities depend on their light-harvesting capacity and trapping efficiency, which

95 ciated with photosystem II (LHCII) to adjust light-harvesting capacity to the prevailing light condit

96 otocatalytic water splitting reaction: solar light harvesting, charge separation and transportation,

97 the largest family of membrane proteins, the light harvesting chlorophyll a/b-binding proteins (LHCPs

98 as highly enriched in the Photosystem (PS) I-light-harvesting chlorophyll (LHC) II supercomplex and d

99 ast SRP (cpSRP) post-translationally targets light-harvesting chlorophyll a/b-binding proteins (LHCP)

100 h are small membrane proteins related to the light-harvesting chlorophyll binding complexes found in

101 subunit (cpSRP43) responsible for delivering light-harvesting chlorophyll binding protein to the thyl

102 r loop abolished loading of the cpSRP cargo, light-harvesting chlorophyll binding protein.

103 d redistribution ("state transition") of the light-harvesting chlorophyll proteins between the two ph

104 posttranslational transport of the abundant light-harvesting chlorophyll-a/b-binding proteins (LHCPs

105 In chloroplasts, the light-harvesting chlorophyll-binding protein (LHCP) in t

106 respiratory subunits in the mitochondria and light-harvesting chlorophyll-binding proteins in chlorop

107 LHC) protein family, which also includes the light-harvesting chlorophyll-binding proteins of photosy

108 of PCPs have been synthesized with different light harvesting chromophores and transition metal bindi

109 a pronounced association of LHCSR3 with PSI-light harvesting complex I (LHCI)-ferredoxin-NADPH oxido

110 The major light harvesting complex II (LHCII) of green plants play

111 in the oxygen-evolving photosystem II (PSII)-light harvesting complex II (LHCII) supercomplex reveals

112 We show that LHCII, the main light harvesting complex of algae, cannot switch to a qu

113 Only genes for light harvesting complex proteins displayed a significan

114 acclimation and requires the accumulation of light harvesting complex stress-related (LHCSR) proteins

115 Light harvesting complex stress-related 3 (LHCSR3) is th

116 te genes of chlorophyll biosynthesis and the light harvesting complex.

117 The light-harvesting complex (LHC) protein family is of para

118 dopsis (Arabidopsis thaliana) belongs to the light-harvesting complex (LHC) protein family, which als

119 uces accumulation of specific members of the light-harvesting complex (LHC) superfamily that contribu

120 ntenna system by the action of two essential light-harvesting complex (LHC)-like proteins, photosyste

121 on of PsaL and PsaH to PSI, both forming the light-harvesting complex (LHC)II docking site of PSI.

122 an over 500-fold fluorescence enhancement of light-harvesting complex 2 (LH2) at the single-molecule

123 lution of chiral electronic structure in the light-harvesting complex 2 of purple bacteria following

124 nly photosystem II antenna proteins, such as LIGHT-HARVESTING COMPLEX B (LHCB).

125 del based on the structure of the main plant light-harvesting complex explains the red-shifted emissi

126 Both trimeric light-harvesting complex II (LHCII) and monomeric LHC pr

127 eracts with Chl catabolic enzymes (CCEs) and light-harvesting complex II (LHCII) at the thylakoid mem

128 Thus, light-harvesting complex II (LHCII) can switch between t

129 Extraction of plant light-harvesting complex II (LHCII) from the native thyl

130 Light-harvesting complex II (LHCII) is a crucial compone

131 The light-harvesting complex II (LHCII) is the main responsi

132 Photosystem II (PSII) core and light-harvesting complex II (LHCII) proteins in plant ch

133 t PSB33 functions in the maintenance of PSII-light-harvesting complex II (LHCII) supercomplex organiz

134 tional redistributions of the major trimeric light-harvesting complex II (LHCII) to balance the relat

135 e dynamic allocation of a mobile fraction of light-harvesting complex II (LHCII) to photosystem II (P

136 em of photosystem II in thylakoid membranes, light-harvesting complex II (LHCII), has a feedback mech

137 ing: DeltapH, the proton gradient (trigger); light-harvesting complex II (LHCII), PSII light harvesti

138 In the major peripheral plant light-harvesting complex LHCII, excitation energy is tra

139 -formation of extensive domains of the major light-harvesting complex of photosystem II and clusterin

140 ed with the absence of photosystem II (PSII) light-harvesting complex protein phosphorylation.

141 LB4, has been proposed to be involved not in light-harvesting complex protein targeting, but instead

142 ing function has been established mainly for light-harvesting complex proteins, which first interact

143 nsitions through the phosphorylation of PSII light-harvesting complex proteins.

144 stead, a small amount of the protein LHCSR1 (light-harvesting complex stress related 1) is able to in

145 hotosystem II subunit S (PSBS) in plants and light-harvesting complex stress-related (LHCSR) in green

146 roteins, Photosystem II Subunit S (PSBS) and Light-Harvesting Complex Stress-Related (LHCSR), are ess

147 e photoprotective states and dynamics of the light-harvesting complex stress-related 1 (LHCSR1) prote

148 her hand, proteins required for NPQ, such as light-harvesting complex stress-related protein1 (LHCSR1

149 tii, known to fully induce the expression of light-harvesting complex stress-related protein3 (LHCSR3

150 ed the first photon antibunching of a single light-harvesting complex under ambient conditions, showi

151 uction in photosystem II, the photosystem II light-harvesting complex, and photosystem I.

152 pen quantum system, such as a photosynthetic light-harvesting complex, approximations are usually mad

153 he phycobilisome (PBS) is an extremely large light-harvesting complex, common in cyanobacteria and re

154 In silico analysis of PSB33 revealed a light-harvesting complex-binding motif within the transm

155 ncy photons by the intermediate units of the light-harvesting complex.

156 he widely studied Fenna-Matthews-Olson (FMO) light-harvesting complex.

157 ed in an application to the phycobiliprotein light harvesting complexes from cryptophyte algae.

158 mediated by a reversible phosphorylation of light harvesting complexes II, depending on the redox st

159 ith the availability of genetically modified light harvesting complexes, to reveal the presence of th

160 ms via the association and disassociation of light-harvesting complexes (LHC) II, in a process known

161 believed to take place in the plant's major light-harvesting complexes (LHC) II, there is still no c

162 Trimers of the PSII light-harvesting complexes (LHCIIs) decreased more than

163 ontrolled, reversible phosphorylation of the light-harvesting complexes (LHCIIs) to regulate the rela

164 The light-harvesting complexes (LHCs), the de-epoxidation of

165 trate strong exciton-photon coupling between light-harvesting complexes and a confined optical mode w

166 ent, accompanied by functional detachment of light-harvesting complexes and interrupted access to pla

167 interaction between specific photosystem II light-harvesting complexes and PSBS in the thylakoids, s

168 Energy relaxation in light-harvesting complexes has been extensively studied

169 efficient energy transfer in photosynthetic light-harvesting complexes is a subject of intense resea

170 e determined crystal structures of three PBP light-harvesting complexes isolated from different speci

171 ve the ultrafast energy relaxation in single light-harvesting complexes LH2 of purple bacteria.

172 The main light-harvesting complexes of diatoms, known as fucoxant

173 latter half of the article, we focus on the light-harvesting complexes of purple bacteria as a model

174 l energy transfer through extended layers of light-harvesting complexes, mimicking the modular antenn

175 iciency, they degrade their large (3-5-MDa), light-harvesting complexes, the phycobilisomes.

176 hlorophylls are comparable to those of other light-harvesting complexes, we anticipate that this find

177 Within the light-harvesting complexes, which frequently have severa

178 tudy energy-transfer processes in biological light-harvesting complexes.

179 kites form an emerging family of exceptional light harvesting compounds.

180 tal material parameter requiring control for light harvesting, conversion and transport technologies,

181 tificial photosynthetic systems that contain light-harvesting coordination complexes may one day repl

182 process, which is of central importance for light harvesting, detection, sensing and photonic data p

183 ct transistors (OFETs), solar cells or other light harvesting devices.

184 c nanostructures, to boost the efficiency of light-harvesting devices through increased light-matter

185 We propose here a new kind of light-harvesting devices using plasmonic nano-antenna gr

186 be applied to the design of novel artificial light-harvesting devices.

187 ed energy transfer can significantly improve light harvesting efficiency of QD devices.

188 For example, higher light-harvesting efficiency can lead to higher photocurr

189 lore the interplay between close-packing and light-harvesting efficiency.

190 e reaction centers and drastically undermine light-harvesting efficiency.

191 active and well-defined catalytic sites on a light-harvesting electrode surface.

192 films were prepared to enhance dye loading, light harvesting, electron transport, and electrolyte po

193 eir constituent nanostructures, and template light-harvesting energy transfer cascades, mediated thro

194 a molecular scale is critical for efficient light harvesting, energy conversion, and nanoelectronics

195 een key processes for photosynthesis, namely light-harvesting, energy transfer, and photoinduced char

196 ands to direct chromophore behavior in large light-harvesting ensembles.

197 are a key design strategy in photosynthetic light harvesting, expanding the spectral cross-section f

198 ghtly increasing the solvent polarity, these light-harvesting fibres disassemble to spherical structu

199 This acclimative response enhances light harvesting for wavelengths complementary to the gr

200 his structural change is significant for the light-harvesting function because it disrupts the strong

201 sign principle for maintaining the efficient light-harvesting function of LHCII in the presence of pr

202 complex a unique strategy to ensure that its light-harvesting function remains robust in the fluctuat

203 y have important implications for biological light-harvesting function.

204 Understanding how photosynthetic light-harvesting functions in the face of these fluctuat

205 e constructed to demonstrate the function of light harvesting in a polymeric nanostructure.

206 tandem configuration for achieving efficient light harvesting in nonfullerene-based OSCs.

207 investigate photophysical phenomena such as light harvesting in photosynthesis in which the system r

208 Reducing excessive light harvesting in photosynthetic organisms may increas

209 Photosynthetic light harvesting in plants is regulated by phosphorylati

210 yanobacteria need to regulate photosynthetic light harvesting in response to the constantly changing

211 ple light scattering and absorption-enhanced light harvesting in the hierarchical structures.

212 s, exhibiting significant enhancement of the light harvesting in the long wavelength regime with resp

213 hich provide remarkable efficiencies through light-harvesting in the strongly sub-wavelength device c

214 Enhanced light harvesting is an area of interest for optimizing b

215 In oxygenic photosynthesis, light harvesting is regulated to safely dissipate excess

216 occurring in natural photosynthesis, namely light harvesting (LH), energy transfer (EnT), reductive/

217 , and, among naturally fluorescing proteins, light-harvesting (LH) proteins from purple bacteria cons

218 Here we investigate the assembly of light-harvesting LH2 and reaction centre-light-harvestin

219 photosynthetic units consisting of arrays of light-harvesting LH2 complexes and monomeric and dimeric

220 -poly(arylene-vinylene) polymer, acting as a light-harvesting ligand system, was synthesized and coup

221 n notable progress using 0-D quantum dots as light harvesting materials.

222 Photocatalytic systems that combine light-harvesting materials and catalysts in solution or

223 m dots (QDs) stand among the most attractive light-harvesting materials to be exploited for solution-

224 rmation can be tuned to offer a new class of light-harvesting materials.

225 Visible light harvesting may be enhanced in other conjugated pol

226 n current approaches to regulating inorganic light-harvesting mimics prevent their use in catalysis.

227 cations in cellular recognition, plasmonics, light harvesting, model systems for membrane protein ass

228 sent a conceptually novel approach to design light-harvesting nanomaterials demonstrating that QD sur

229 vances and the current status of challenging light-harvesting nanomaterials, such as semiconducting q

230 ch, whereby we combined the highly efficient light harvesting of inorganic semiconductors with the hi

231 h as nano-enhanced plasmonics and catalysis, light harvesting, or phase transitions.

232 re considered to be among the most efficient light-harvesting organisms.

233 w of the latest progress in energy transfer, light-harvesting, photocatalytic proton and CO2 reductio

234 ufQBALMX operon encoding the reaction centre-light-harvesting photosystem complex.

235 illations have been reported for the soluble light-harvesting phycobiliprotein (PBP) antenna isolated

236 ggesting that PhiCpeT may also help assemble light-harvesting phycobiliproteins during infection.

237 ction in energy transfer between the soluble light harvesting phycobilisome complex and membrane-boun

238 cells of DeltarpoZ were not able to increase light-harvesting phycobilisome antenna like CS upon high

239 dissipation of excess energy absorbed by the light-harvesting phycobilisomes (PBS) in cyanobacteria.

240 to contain anthocyanin which is an excellent light harvesting pigment needed for the generation of ch

241 Phycoerythrin is a major light-harvesting pigment of red algae, which could be us

242 nt importance for this function and can form light-harvesting pigment protein complexes.

243 than 200 prosthetic groups, which are mostly light harvesting pigments.

244 tection for both the reaction centre and the light-harvesting pigments of the antenna.

245 is group possesses a remarkable diversity of light-harvesting pigments, and most of the group's membe

246 tem is constructed by controlled assembly of light-harvesting plasmonic nanoantennas onto a typical p

247 d with the production of reaction centre and light-harvesting polypeptides.

248 al for the assembly of higher molecular mass light-harvesting PORB::PORA complexes and photoprotectio

249 he role played by the organic cations in the light-harvesting process remaining unclear.

250 ansfer-to-the-trap limitation of the overall light-harvesting process.

251 roelectricity and electrical conductivity or light-harvesting properties coexist in a single compound

252 ization plays a critical role in shaping the light-harvesting properties of many photosynthetic pigme

253 triazine and porphyrin faces with promising light-harvesting properties.

254 lants and is necessary for the regulation of light harvesting, protection from oxidative stress and a

255 lation, thereby activating the repression of light-harvesting protein synthesis, which is needed to c

256 light supply, which permits accumulation of light-harvesting proteins and efficient light capture.

257 or a modulated expression of nucleus-encoded light-harvesting proteins associated with photosystem II

258 s/molecular mechanics (QM/MM) simulations of light-harvesting proteins from oxygenic (LHCII) and anox

259 stness and high efficiency of photosynthetic light-harvesting proteins.

260 aic reaction centers are embedded throughout light-harvesting regions of the device.

261 This links the protein dynamics to the light-harvesting regulation in plants by the carotenoids

262 Light-harvesting regulation is important for protecting

263 Effectiveness of molecular-based light harvesting relies on transport of excitons to char

264 genase molybdenum-iron (MoFe) protein, where light harvesting replaces ATP hydrolysis to drive the en

265 um) purple bacteria are known to adapt their light-harvesting strategy during growth according to env

266 ramolecular, nanotubular structures in large light-harvesting structures called chlorosomes.

267 The design of optimal light-harvesting (supra)molecular systems and materials

268 Light harvesting supramolecular assemblies are potential

269 s approach, we fabricate a multichromophoric light harvesting system that would be unattainable by tr

270 s was increased by more than 3 times using a light harvesting system.

271 ll-defined and spectrally tunable artificial light-harvesting system has been constructed in which mu

272 r phycobilisomes and the regulation of their light-harvesting system in general.

273 nomer, multiple tryptophans form an extended light-harvesting system in which the La excited state of

274 ited state energy transfer in photosynthetic light harvesting systems.

275 Potential light-harvesting systems based on dye-doped pi-conjugate

276 pyrrole-based architectures for panchromatic light-harvesting systems for solar-energy conversion.

277 Artificial light-harvesting systems have until now not been able to

278 st step toward developing more complex model light-harvesting systems integrated with reaction center

279 They contain a unique combination of light-harvesting systems represented by a membrane-bound

280 Natural light-harvesting systems spatially organize densely pack

281 is crucial for the development of efficient light-harvesting systems, like photocatalytic and photov

282 t properties of other natural and artificial light-harvesting systems.

283 me scale, rivaling transfer rates in natural light-harvesting systems.

284 importance for the development of efficient light-harvesting systems.

285 s are versatile synthetic models for natural light-harvesting systems.

286 and informing rational design of artificial light-harvesting systems.

287 coupled exciton dynamics present in natural light-harvesting systems.

288 porphyrin-based nanostructures for potential light-harvesting systems.

289 rface energy transfer process for developing light-harvesting systems.

290 ards to applications in opto-electronics and light harvesting; tailored enhancement of such plasmons

291 ent of doped CQWs in LSCs for advanced solar light harvesting technologies.

292 embedding planar THz antennas for efficient light harvesting, the first technological demonstration

293 al for becoming a powerful tool for enhanced light harvesting, the slow-photon effect, a manifestatio

294 r efficiencies of 83% and a small functional light-harvesting unit.During photosynthesis, energy is t

295 developed multiple strategies for balancing light-harvesting versus intracellular energy utilization

296 osynthetic machinery allosterically regulate light harvesting via conformational and electronic chang

297 cement and introducing future challenges for light harvesting, vibrational spectroscopy, imaging, and

298 , reflection and antireflection, scattering, light harvesting, wave guiding and lensing, camouflage,

299 nergy transfer (FRET) enables photosynthetic light harvesting, wavelength downconversion in light-emi

300 the level of chlorophyll excited states from light harvesting with the rate of electron transport fro