ライフサイエンスコーパス: energy transfer

1 one or many traces (e.g., Forster resonance energy transfer).

2 ffolds to achieve highly efficient, directed energy transfer.

3 ic antenna to reaction centers via ultrafast energy transfer.

4 racts of B-form DNA while retaining coherent energy transfer.

5 -time measurements of fluorescence resonance energy transfer.

6 honon polaritons enable efficient near-field energy transfer.

7 re vibrations upon electronic excitation and energy transfer.

8 requires the vicinity of these two ions for energy transfer.

9 zed as amplified energy transfer or multiple energy transfer.

10 with delocalised excitons from intercluster energy transfer.

11 s confirm the role of photosensitization via energy transfer.

12 y probe an extensive range in wavevector and energy transfer.

13 to changes in the non-radiative damping and energy transfer.

14 ermolecular Tb(III)-to-dye Forster resonance energy transfer.

15 ather weak interchain excitonic coupling and energy transfer.

16 arylation across a panoply of substrates by energy transfer.

17 s was confirmed using fluorescence resonance energy transfer.

18 through endothermic reverse triplet-triplet energy transfer.

19 nsiderably faster and more robust excitation energy transfer.

20 to Nav1.4 through Lanthanide-based Resonance Energy Transfer.

21 ns; bond-breaking; and electron, proton, and energy transfers.

22 were studied using bioluminescence resonance energy transfer 2 (BRET(2)) in STHdh(Q7/Q7) cells.

23 bition of receptor bioluminescence resonance energy transfer and bimolecular fluorescence complementa

24 photon emission, the distance dependence of energy transfer and carrier diffusion have been investig

25 to elucidate the fundamental dynamics of the energy transfer and charge separation processes of these

26 Here, we investigated excitation energy transfer and charge separation using this FRL-gro

27 ntimate relationship between triplet-triplet energy transfer and charge transfer.

28 ls with time-resolved fluorescence resonance energy transfer and death assays, and show remarkable ag

29 rison with single-molecule Forster Resonance Energy Transfer and ensemble measurements revealed that

30 udies substantiated the mechanism of triplet energy transfer and explained the unusual regiocontrol.

31 the main emphasis on the characterization of energy transfer and its role in dictating device archite

32 rk, a novel combination of Forster resonance energy transfer and Monte Carlo simulations (MC-FRET) id

33 y be obtained from the simulations regarding energy transfer and peptide-H(+) surface-induced dissoci

34 Alpha-particle emitters have a high linear energy transfer and short range, offering the potential

35 issue PDT via red-shifted porphyrin Q-bands, energy transfer and sonodynamic effects, and enable new

36 of excess anthracene in solution, efficient energy transfer and subsequent triplet-triplet annihilat

37 -encoded light-absorbers, thereby augmenting energy transfer and trapping in photosynthesis.

38 cules capable of performing highly efficient energy transfer and ultrafast photoinduced electron tran

39 orescence complementation, Forster resonance energy transfer, and coimmunoprecipitation approaches re

40 uate complex dynamics such as photosynthetic energy transfer, and complements traditional global and

41 d with immunoassays or fluorescent resonance energy transfer, and contractility was determined in car

42 ring, single-molecule fluorescence resonance energy transfer, and NMR) indicate that HIPK1-PAGE4 exhi

43 eflection fluorescence microscopy, resonance energy transfer, and proximity biotinylation.

44 f atomic force microscopy, Forster resonance energy transfer, and small-angle x-ray scattering data o

45 y useful phenomena, such as highly efficient energy transfer, anomalous single particle blinking, and

46 cross-linking and bioluminescence resonance energy transfer approaches, we found that PiT1 and PiT2

47 ased on exciton theory and Forster resonance energy transfer are explored.

48 tes originating from FRET (Forster Resonance Energy Transfer) are powerful tool for examining the act

49 pendent phenomena, such as Forster resonance energy transfer, are important interactions for use in s

50 BODIPY-hydroporphyrin energy transfer arrays allow for development of a family

51 A series of energy transfer arrays, comprising a near-IR absorbing a

52 rate net optical amplification and Brillouin energy transfer as the basis for flexible on-chip light

53 a novel time-resolved fluorescence resonance energy transfer assay, and correlated these properties w

54 Bioluminescence resonance energy transfer assays for Gi activation and arrestin-3

55 Furthermore, bioluminescent energy transfer assays indicated that while Galphao inte

56 oprecipitation and bioluminescence resonance energy transfer assays.

57 hat can be used in bioluminescence resonance energy transfer assays.

58 proteins that are FRET pairs exhibit robust energy transfer at the plasma membrane.

59 This aptasensor enables the energy transfer based on a fluorescence resonance energy

60 theoretical models for amplified or multiple energy transfer based on exciton theory and Forster reso

61 Our upconversion nanoparticle resonance energy transfer based sensor with polyethylenimine-coati

62 ticles (UCNPs) are attractive candidates for energy transfer-based analytical applications.

63 recently developed bioluminescence resonance energy transfer-based approach involving fusion of the R

64 ese, we used a set of fluorescence resonance energy transfer-based biosensors for different RhoGTPase

65 c mice expressing the fluorescence resonance energy transfer-based cGMP biosensor cGi500, NO-induced

66 ur knowledge, a novel fluorescence resonance energy transfer-based measurement of the binding kinetic

67 added to a sensitive fluorescence resonance energy transfer-based tau uptake assay to assess blockin

68 This orthodox picture of incoherent energy transfer between clusters of a few pigments shari

69 a substantial amount of FRET is generated by energy transfer between fluorophores located in separate

70 Furthermore, the energy transfer between host CdS QDs and dopants can be

71 we show time-resolved fluorescence resonance energy transfer between receptor glycans and fluorescent

72 In this Perspective, we examine energy transfer between semiconductor nanocrystals (NCs)

73 ted state is involved in efficient and rapid energy transfer between the electronic system and the la

74 that there is a strong spectral overlap and energy transfer between the infrared luminescence of Er(

75 to weak absorption overlap and thus limited energy transfer between the plasmonic metal and the semi

76 s-less coupling and thus coherent ultra-fast energy transfer between the remote partners.

77 Multiplexed bioluminescence resonance energy transfer (BRET) assays were developed to monitor

78 ptors by real-time bioluminescence resonance energy transfer (BRET) assays.

79 Using bioluminescence resonance energy transfer (BRET) in live cells, we show that WNT5A

80 We utilized bioluminescence resonance energy transfer (BRET) to detect and quantify assembly o

81 We have used bioluminescence resonance energy transfer (BRET) to study the Arf1/AP-1 interactio

82 , as determined by bioluminescence resonance energy transfer (BRET)-based saturation and kinetic bind

83 emiconductor structure and show that exciton energy transfer can be extended to tens of microns, medi

84 spontaneous emission, scattering and Forster energy transfer) can be controlled by nonlocal dielectri

85 ments, we identify an efficient out-of-plane energy transfer channel, where charge carriers in graphe

86 This method is based on Forster resonance energy transfer combined with fluorescence quenching.

87 the interpretation of fluorescence resonance energy transfer data.

88 rformed time-resolved fluorescence resonance energy transfer, directly detecting structural changes w

89 end this review with a brief overview of the energy-transfer dynamics and pathways in the light-harve

90 In this electrochemiluminescence resonance energy transfer (ECL-RET) approach, Fe3O4@SiO2/dendrimer

91 anisms regulate the efficiency of excitation energy transfer (EET) to fit light energy supply to bioc

92 l as the mechanisms of electronic excitation energy transfer (EET).

93 due to Trp-NAD(P)H interactions, correlating energy transfer efficiencies (E%) vs NAD(P)H-a2%/FAD-a1%

94 noscale surface texturing can lead to higher energy transfer efficiencies, substantial energy savings

95 hat Top2 binds and bends DNA to increase the energy transfer efficiency (EFRET), and ATP treatment fu

96 ramids are expected to predominate, based on energy transfer efficiency [2] and empirical evidence fr

97 By studying the energy transfer efficiency from the various AuNP conjuga

98 ctively, but also a higher biomass yield and energy transfer efficiency relative to Nitrobacter spp.

99 (PPCs) that can modulate the donor-acceptor energy transfer efficiency with exceptional precision by

100 the long lifetime is not cut short upon high energy-transfer efficiency.

101 They also demonstrate energy transfer (ET) acceptor/sensitization properties w

102 preciated is their growing role as versatile energy transfer (ET) donors and acceptors within a simil

103 hybrid material with rapid ligand-to-ligand energy transfer (ET).

104 - and intermolecular proton-, electron-, and energy transfer events of the guest within the SBMs.

105 ectron resonance, and fluorescence resonance energy transfer experiments applied to IDPs.

106 confounding factor in fluorescence resonance energy transfer experiments measuring arm closure rates

107 Bioluminescence resonance energy transfer experiments proved that this compound wa

108 nly used acceptor agent in Forster resonance energy transfer experiments that allows the study of hig

109 y simulations, single-pair Forster resonance energy transfer experiments, and existing NMR data, we d

110 nor-acceptor pairs in fluorescence resonance energy transfer experiments, especially those involving

111 ere, using single-molecule Forster resonance energy transfer experiments, we show that both SpCas9-HF

112 We developed a novel Forster resonance energy transfer-fluorescence lifetime imaging microscopy

113 r dissociation routes made available through energy transfer following the eventual decay of LSPRs.

114 oprecipitated, and in-cell Forster resonance energy transfer (FRET) and glutathione S-transferase pul

115 hich have been ascribed to Forster resonance energy transfer (FRET) and, to a lesser extent, nanosurf

116 ere, we use a quantitative Forster resonance energy transfer (FRET) approach to show that Ecadherin f

117 ticle size measurement and forster resonance energy transfer (FRET) approach.

118 oded sensors based on fluorescence resonance energy transfer (FRET) are powerful tools for quantifyin

119 ere we describe a time-resolved fluorescence energy transfer (FRET) assay reporting membrane expressi

120 ing a novel flow cytometry-Forster resonance energy transfer (FRET) assay.

121 munoprecipitation and fluorescence resonance energy transfer (FRET) assays, we now show the PBM direc

122 ng a highly sensitive Fluorescence Resonance Energy Transfer (FRET) based assay.

123 (from development of fluorescence resonance energy transfer (FRET) between phycoerythrin-biotin (Phy

124 ver, the Forster (or fluorescence) resonance energy transfer (FRET) between the C-dots and EtBr was s

125 Using a fluorescence resonance energy transfer (FRET) biosensor, we show that a phospho

126 The performance of Forster Resonance Energy Transfer (FRET) biosensors depends on brightness

127 maging near-infrared (NIR) Forster resonance energy transfer (FRET) both in vitro and in vivo.

128 l substrates based on Fluorescence Resonance Energy Transfer (FRET) for the MPR by employing computat

129 y transfer based on a fluorescence resonance energy transfer (FRET) from the QDs to the GO sheets, qu

130 The single-molecule Forster resonance energy transfer (FRET) is a powerful tool to study inter

131 ve this conundrum, we used Forster resonance energy transfer (FRET) measured by fluorescence lifetime

132 k and single-molecule fluorescence resonance energy transfer (FRET) methods to investigate a set of t

133 ticle synthesis method and Forster resonance energy transfer (FRET) microscopy imaging to visualize n

134 Forster resonance energy transfer (FRET) microscopy is a powerful techniqu

135 ded by genetically encoded Forster resonance energy transfer (FRET) nanosensors.

136 further show that a simple Forster resonant energy transfer (FRET) network model accurately predicts

137 that QDs provide as either Forster resonance energy transfer (FRET) or charge/electron transfer donor

138 competitive and sequential Forster resonance energy transfer (FRET) pathways between QDs and fluoresc

139 denaturing conditions, two Forster resonance energy transfer (FRET) populations were observed that co

140 -based intramolecular fluorescence resonance energy transfer (FRET) probe, which previously allowed u

141 cose in tear by using fluorescence resonance energy transfer (FRET) quenching mechanism.

142 cation was enabled using a Forster Resonance Energy Transfer (FRET) relationship between the photochr

143 By measuring of fluorescence resonance energy transfer (FRET) signals between CDs and AuNPs as

144 Forster resonance energy transfer (FRET) studies performed at the single m

145 We use single-molecule Forster resonance energy transfer (FRET) to measure the global reconfigura

146 aveguides (ZMWs) with fluorescence resonance energy transfer (FRET) to resolve single-molecule associ

147 ingle-molecule three-color Forster resonance energy transfer (FRET) tracking methods.

148 Forster resonance energy transfer (FRET) using fluorescent base analogues

149 rotein interactions, using Forster resonance energy transfer (FRET), confocal microscopy, and intrace

150 his work, a combination of Forster resonance energy transfer (FRET), nonreducing SDS-PAGE, and strate

151 ling based on in vivo fluorescence resonance energy transfer (FRET), small-angle x-ray scattering (SA

152 Also, by using fluorescence resonance energy transfer (FRET), we demonstrate increased interac

153 FR biosensor based on fluorescence resonance energy transfer (FRET), which can detect the real-time P

154 Studies with a fluorescence resonance energy transfer (FRET)-based alpha-catenin conformation

155 Here, we employed fluorescence resonance energy transfer (FRET)-based biosensors in conjunction w

156 herefore, we targeted fluorescence resonance energy transfer (FRET)-based biosensors toward subcellul

157 c mitochondrially targeted Forster resonance energy transfer (FRET)-based calcium indicator (4mtD3cpv

158 ardiomyocytes expressing a Forster resonance energy transfer (FRET)-based cAMP biosensor, we confirme

159 Here, we present a set of Forster resonance energy transfer (FRET)-based crowding-sensitive probes a

160 Here we present a fluorescence resonance energy transfer (FRET)-based sensor, CUTie, which detect

161 While fluorescence resonance energy transfer (FRET)-based sensors for these kinases h

162 reverse-transcription fluorescence resonance energy transfer (FRET)-PCR.

163 Tunable Forster resonance energy transfer (FRET)-quenched substrates are useful fo

164 articles (Au NPs) via fluorescence resonance energy transfer (FRET).

165 l suited as donors in fluorescence resonance energy transfer (FRET).

166 fetime as a clear hint for Forster resonance energy transfer (FRET).

167 r for NE activity based on Forster resonance energy transfer (FRET).

168 lated to HIV based on fluorescence resonance energy transfer(FRET) between carbon dots(CDs) and AuNPs

169 ic catalysis via such an activation pathway: Energy transfer from an iridium sensitizer produces an e

170 fluorescence studies supported an efficient energy transfer from BODIPY unit(s) to azaBODIPY unit in

171 dynamically excited through non-equilibrium energy transfer from highly energetic protons in liquid

172 mine the underlying mechanisms of sequential energy transfer from laser light to nanoparticle to flui

173 Here, we demonstrate efficient energy transfer from near-infrared-emitting ortho-mercap

174 version mechanism, allowing cascaded exciton energy transfer from one transition metal dichalcogenide

175 metals, the physical mechanisms that govern energy transfer from plasmonic metals to catalytic metal

176 Plasmon resonance energy transfer from the Au NPs to the CdSe QDs, which e

177 The results demonstrated an efficient energy transfer from the excited Coumarin 2 to the groun

178 lts from a near quantitative triplet-triplet energy transfer from the nanocrystals to 1-pyrenecarboxy

179 tor via an upconversion process utilizing an energy transfer from the nanoparticle to the indicator.

180 of the magnetisation response depends on the energy transfer from the photons to the spins during the

181 biological pathways including transcription, energy transfer, functional aptamers and RNA interferenc

182 e accurate description of the photosynthetic energy transfer functioning and subsequent applications

183 Efficient energy transfer (>0.90) is observed for each dyad, which

184 ough the utility of triplet sensitization by energy transfer has long been known as a powerful activa

185 rs, including photochromic Forster resonance energy transfer, high-resolution microscopy, and live tr

186 y and single-molecule fluorescence resonance energy transfer imaging to elucidate the structures and

187 using single-molecule fluorescence resonance energy transfer imaging, we examine TM6 movements in the

188 Finally, using fluorescence resonance energy transfer imaging, we found that cocaine tolerance

189 approaches, including fluorescence resonance energy transfer imaging, we found that the influx of ext

190 nce/Cerenkov luminescence/Cerenkov radiation energy transfer) imaging for rapid and accurate delineat

191 Using bioluminescence resonance energy transfer, immunofluorescence microscopy, and co-i

192 ng can enrich our understanding of nanoscale energy transfer in molecular excitonic systems and may d

193 rated photonic and plasmonic devices.Exciton energy transfer in monolayer transition metal dichalcoge

194 Here the authors track energy transfer in photosynthetic bacteria using two-dim

195 model Hamiltonians to describe excited state energy transfer in photosynthetic light harvesting syste

196 ly couple to phonons and vibrations, such as energy transfer in photosynthetic pigment-protein comple

197 bottom-up model of pigment organization and energy transfer in phycobilisomes is essential to unders

198 re expected to be important for facilitating energy transfer in the Fenna-Matthews-Olson (FMO) comple

199 and open questions regarding the physics of energy transfer in this regime.

200 Energy transfer in vivo is primarily monitored by measur

201 The description of energy transfer, in particular multichromophoric antenna

202 Today's understanding of the energy transfer includes the fact that the excitons are

203 Molecular control of energy transfer is an attractive proposition because it

204 to the orange polymers via Forster or Dexter energy transfer is analyzed through time resolved photol

205 er transition metal dichalcogenides, exciton energy transfer is typically limited to a short range (

206 Linear energy transfer (LET) has been scored from energy deposi

207 cts (NTE) occur for low doses of high linear energy transfer (LET) radiation, leading to deviation fr

208 lution for particle range, energy and linear energy transfer (LET).

209 sorbed (physical) dose and the proton linear energy transfer (LET).

210 nsor domain using lanthanide-based resonance energy transfer (LRET) between the rat skeletal muscle v

211 lows for upconversion luminescence resonance energy transfer (LRET) that can be used to quantify the

212 Here, we used luminescence resonance energy transfer (LRET) to measure the distances between

213 Forster resonance energy transfer mapping of key residues within this tern

214 Fluorescence resonance energy transfer measurements in cells transiently transf

215 Bioluminescence resonance energy transfer measurements in live cells reveal that K

216 of-the-art single-molecule Forster resonance energy transfer measurements on biologically relevant, m

217 Fluorescence resonance energy transfer measurements, combined with PG-binding a

218 on of single-molecule fluorescence resonance energy transfer measurements, where the observed dynamic

219 endant ytterbium(III) cations, a Dexter-type energy transfer mechanism is suggested, which is an impo

220 istic dichotomy via both singlet and triplet energy transfer mechanisms.

221 and a recently introduced Forster resonance energy transfer microscopy method, fully quantified spec

222 e intensity matched a homo-Forster Resonance Energy Transfer model.

223 fferential centrifugation, Forster resonance energy transfer, native electrophoresis, and chemical cr

224 , maximizing the efficiency of non-radiative energy transfer (NRET) between the donor and the accepto

225 of MoS2 excitonic PL enabled by nonradiative energy transfer (NRET) from adjacent nanocrystal quantum

226 (FRET) and, to a lesser extent, nanosurface energy transfer (NSET).

227 30 nm, rapid and quantitative intramolecular energy transfer occurs from the (1*)ExBIPY(2+) unit to t

228 S) with the photoCORM and shining red light, energy transfer occurs from triplet excited-state (3)PS*

229 MD2 also decreased bioluminescence resonance energy transfer of APJ dimer.

230 rk for modeling the absorption, emission and energy transfer of incoherent radiation between cascade

231 dent exciton decay dynamics and photoinduced energy transfer of QDs is addressed.

232 ssibility that chlorophyll f participates in energy transfer or charge separation is discussed on the

233 c system, and are characterized as amplified energy transfer or multiple energy transfer.

234 d to triplet excited-state quenching via (1) energy transfer or paramagnetic quenching by the Co(II)

235 their use as scaffolds to assemble multiple energy transfer pathways.

236 supercapacitors possess high specific power (energy transferred per unit mass per unit time) and can

237 lectivity provided by photo-induced electron/energy transfer (PET) activation to develop efficient si

238 Energy transfer phenomena between Mn(2+) and Yb(3+) occu

239 he optical sensing principle is based on the energy transfer phenomenon that occurs between photoexci

240 m yields of (3)DOM, measured by electron and energy transfer probes, and (1)O2 decreased with molecul

241 pact of the metal-nanoparticle-based surface energy transfer process for developing light-harvesting

242 electronic spectroscopy to follow the entire energy transfer process in a thriving culture of the pur

243 In order to identify the mechanism of this energy transfer process, the distance of the ytterbium(I

244 Such systems are always based on an energy-transfer process from a chemiluminescent precurso

245 -exclusion chromatography, Forster resonance energy transfer, pulldown, and in vitro GEF assays to de

246 ntroducing a homogeneous quenching resonance energy transfer (QRET) technique-based screening strateg

247 ted state of each complex was estimated from energy-transfer quenching experiments using a series of

248 We find that the exciton energy transfer range can be extended to tens of microns

249 citation power densities, we observed faster energy transfer rates under stronger excitation conditio

250 ay rates, Van der Waals forces and resonance energy transfer rates, are conventionally limited to the

251 343 in the core, with the efficiency of the energy transfer reaching as high as 98 %.

252 strategy is presented to utilize a resonance energy transfer (RET) mechanism to construct a novel dya

253 Consecutive resonance energy transfers (RETs) may be accessed due to the avail

254 using recombinant-targeted Forster resonance energy transfer sensors, we show that hyperglycemia indu

255 The Forster resonance energy transfer signal between CPT and maleimide thioeth

256 -tRNA single-molecule fluorescence resonance energy transfer signal, we directly observe the conforma

257 Single-molecule fluorescence resonance energy transfer (smFRET) analyses indicate the NIS of ki

258 eling with single molecule Forster resonance energy transfer (smFRET) and catalytic activity measurem

259 Using single-molecule fluorescence resonance energy transfer (smFRET) between (Cy5)EF-G and (Cy3)tRNA

260 Single-molecule Forster resonance energy transfer (smFRET) experiments using donor-labeled

261 e used single-molecule florescence resonance energy transfer (smFRET) experiments, classical molecula

262 e used the single-molecule Forster resonance energy transfer (smFRET) method to observe the open and

263 have used single molecule Forster Resonance Energy Transfer (smFRET) to examine the real time nucleo

264 ated using single-molecule Forster resonance energy transfer (smFRET).

265 oprecipitation and bioluminescence resonance energy transfer studies confirmed that 5-HT2C receptors

266 Using live-cell fluorescence resonance energy transfer studies, we demonstrated that soluble EC

267 Here we report a unique energy-transfer system, where the sensitized acceptor em

268 n for the incorporation of emissive AuNPs in energy transfer systems.

269 w, chlorophyll-to-carotenoid triplet-triplet energy transfer (T-TET) is slow, in the tens of nanoseco

270 ase assay with the bioluminescence resonance energy transfer technique suggested that multiple (at le

271 uciferase assay, a bioluminescence resonance energy transfer technique, and site-directed mutagenesis

272 sing mass spectrometry and Forster resonance energy transfer techniques, we confirm and characterize

273 l on PbS quantum dots (QDs) enhances triplet energy transfer (TET) by suppressing competitive charge

274 Since triplet energy transfer (TET) from NC donors to molecular transm

275 The efficiency of triplet energy transfer (TET) from the CdSe NC donor to a diphen

276 to the cells are the dominant mechanisms of energy transfer that results in intracellular uptake of

277 Rather than facilitating intertrimer energy transfer, the close associations between PSI prim

278 urrent generation is enhanced by directional energy transfer through extended layers of light-harvest

279 scattered light, we extract the dynamics of energy transfer through the dense network of antenna com

280 Different mechanisms have been proposed: energy transfer to a lutein quencher in trimers, formati

281 ion of BODIPY at 500 nm results in efficient energy transfer to and bright emission of hydroporphyrin

282 Here we use Forster resonance energy transfer to characterize the energetics of homo-

283 irected time-resolved fluorescence resonance energy transfer to determine the effect of a pathologica

284 used single-molecule fluorescence resonance energy transfer to directly observe conformational chang

285 the UCNP shell containing Nd and subsequent energy transfer to Er in the Core to produce efficient g

286 used single-molecule fluorescence resonance energy transfer to monitor tertiary structure formation

287 of nanoparticles remains suppressed owing to energy transfer to the chromophore.

288 The subsequent energy transfer to the reaction center is commonly ratio

289 of the time-resolved fluorescence resonance energy transfer (TR-FRET) assay was 9.6 ng/mL, and the l

290 using a time-resolved fluorescence resonance energy transfer (TR-FRET) technology, to identify revers

291 ilizing time-resolved luminescence resonance energy transfer (TR-LRET) was developed for the detectio

292 Ecologically, they influence energy transfer vertically through trophic levels and so

293 region (QX) absorption bands of the RC allow energy transfer via a Forster mechanism, with an efficie

294 (Zn(i + 2)-Zn(i + 6)), and highly efficient energy transfer was demonstrated with estimated efficien

295 Bioluminescence resonance energy transfer was employed to analyze how receptor mut

296 Based on the observed Forster resonance energy transfer, we determined that upon photoconversion

297 Using time-resolved fluorescence resonance energy transfer, we provide, to our knowledge, the first

298 Using single-molecule Forster resonance energy transfer, we show that Psi56 dampens conformation

299 ory dramatically underestimated the observed energy transfer while NSET-based damping models provided

300 quenching, enhancement, or Forster resonance energy transfer with transport methods.