ライフサイエンスコーパス: FRET

1 FRET analyses indicated that the C-terminal TnT region a

2 FRET and surface pulldown studies in cell lines revealed

3 FRET experiments can provide state-specific structural i

4 FRET is a powerful approach to study the interactions of

5 FRET-based experiments revealed that the selective P2Y(1

6 gainst X-ray structures for sets of 15 to 23 FRET pairs.

7 The use of 33 FRET-derived distance sets, to screen available T4L stru

8 assays, LC-MS/MS-based proteomics, and CCF-4 FRET analysis, we obtained evidence that the N (alpha)-a

9 A FRET-based high throughput screening identified NSC62260

10 ements on multiple green-red biosensors as a FRET acceptor and is an efficient FRET donor that suppor

11 confocal microscopy was used to calibrate a FRET-based Pi sensor to determine absolute, rather than

12 In this study, we constructed a FRET probe composed of yellow fluorescent protein attach

13 leavage of phosphodiester bonds by TDP1 in a FRET assay with an IC(50) of 190 nM.

14 er (smFRET) to measure the conformation of a FRET labelled E2~Ub conjugate, which distinguishes betwe

15 chromophore distance were quantified using a FRET model.

16 Using a FRET-based assay, we examined the stability of the alpha

17 Using a FRET-based biosensor, we monitored ERK signalling dynami

18 Using a FRET-based high-throughput screening assay that we previ

19 FR1, VEGFR2-FGFR2, and VEGFR2-FGFR3, using a FRET-based method.

20 We utilized a FRET approach to examine the kinetics of structural chan

21 mically labeled ligands or antibodies with a FRET (fluorescence resonance energy transfer) probe to g

22 The FRET probes, with a FRET efficiency of ~20% at physiological pH of 7.0, have

23 fter OAG as well as GSK-1702934A activation, FRET efficiency was simultaneously and significantly red

24 Additionally, FRET experiments indicate an expansion of p27 throughout

25 derations are also given for FRET assays and FRET imaging, especially with fluorescent proteins.

26 citation wavelength and in situ assembly and FRET to mCherry demonstrate the versatility of the TG-FR

27 yield comparable or improved brightness and FRET coupling within a small volume.

28 ), fluorescence lifetime imaging (FLIM), and FRET analyses, we found that substituting the correspond

29 rmal calorimetry analysis, fluorescence, and FRET quenching, and a range of K(d) values were determin

30 uorescence, siRNA-based gene knockdowns, and FRET-based biosensor reporter assays, we investigated th

31 including immunofluorescence microscopy and FRET analyses, we demonstrate that the proto-oncogene c-

32 etection, EPR spectroscopy, mutagenesis, and FRET-positioning and screening, and other biochemical an

33 s are sufficient to reconcile prior SAXS and FRET studies, thus providing a unified picture of the na

34 Complementary MD simulations and FRET experiments showed that open-to-closed transitions

35 chment and isolation by magnetic sorting and FRET-based flow sorting.

36 oscopy to measure the oligomer stability and FRET efficiency for homo- and hetero-oligomers of fluore

37 Using stopped-flow techniques and FRET-melting/annealing assays, we confirmed that the rat

38 We demonstrate photoswitching anisotropy FRET (psAFRET) with a number of test chimeras and exampl

39 tems, allowing for the interpretation of any FRET system conjugated to protein or ribonucleoprotein c

40 plenocytes and human macrophages, as well as FRET-based kinetic and equilibrium binding assays.

41 Using liposome fusion assays, FRET and NMR spectroscopy, here we provide a comprehensi

42 Using this J-aggregate-based FRET method, dye-core-polymer-shell nanoparticles showed

43 ridized with a short oligonucleotide bearing FRET acceptor ATTO647N.

44 fficed for Ca(2+) feedback, yet biochemical, FRET, and structural studies showed that multiple CaM mo

45 Biophysical FRET analyses suggest an unconventional co-distribution

46 ate Src, which was further confirmed by both FRET and western blotting.

47 RET probe was expressed in human cells, both FRET efficiency and fluorescence intensity in the nucleu

48 ts ratiometric response to the target DNA by FRET acceptor displacement and enables DNA detection in

49 Overall, non-invasive VRAC measurement by FRET is an essential tool for unraveling its activation

50 propagation of tau aggregation monitored by FRET.

51 olecular dynamics simulations with live-cell FRET and secondary messenger measurements, for 21 GPCR-G

52 bsent or photobleached, from which two-color FRET data is collected in the same experiment.

53 Furthermore, combining FRET data with small-angle X-ray scattering (SAXS) model

54 opomyosin-TnT crystal structures and complex FRET measurements during model construction.

55 The concept of this multi-component FRET/NSET fluorescence quenching system can be extended

56 e acceptor significantly affect conventional FRET calculations.

57 stingly, protein kinase inhibition decreases FRET efficiency in guard cells, providing direct experim

58 rol experiments to unambiguously demonstrate FRET and validate that the experiments provide meaningfu

59 Proximity-dependent FRET could be monitored directly after or during (real-t

60 e accurately estimated from the CLSM derived FRET ratio.

61 rate and quantify the signals from different FRET-based biosensors to simultaneously measure changes

62 d human cell lines with a designer disulfide FRET probe.

63 ver, time-gated FRET imaging with the Ln-dye FRET pairs efficiently suppressed sample autofluorescenc

64 with a stretched exponential decay model (<E(FRET)(exp)> = 0.25 +/- 0.05) and those calculated from t

65 from the molecular dynamics simulations (<E(FRET)(MD)> = 0.18 +/- 0.14).

66 that can be tailored and optimized for each FRET pair.

67 stributions and relative populations of each FRET level based on the assigned kinetic model and to di

68 tion rates, and relative populations of each FRET level based on the assigned kinetic model.

69 nsors as a FRET acceptor and is an efficient FRET donor that supports red/far-red FRET biosensing.

70 ), and bearing 65 acceptors, shows efficient FRET with >20% quantum yield and a signal amplification

71 ion of the MKK7gamma PIIVIT motif eliminated FRET with CaN and promoted MKK7gamma redistribution to t

72 To address this, we used genetically encoded FRET biosensors of molecular tension in a nesprin protei

73 cytometry in conjunction with an engineered FRET reporter called VIral ProteasE Reporter (VIPER) to

74 multiple single-molecule and in-gel ensemble FRET assays.

75 rster resonance energy transfer experiments (FRET) supported the theoretical predictions.

76 olution fluorescence lifetime imaging (FLIM)-FRET of HeLa cells to identify protein interactions with

77 Time-domain FLIM-FRET measurements of these dynamic interactions are part

78 Transient kinetic analysis and stopped-flow FRET demonstrated that the R712G mutation slowed the max

79 cterized through changes in the fluorescence FRET ratio and validated with isothermal titration calor

80 ve structure, (ii) an efficient approach for FRET-assisted coarse-grained structural modeling, and al

81 Some considerations are also given for FRET assays and FRET imaging, especially with fluorescen

82 suite with (i) an automated design tool for FRET experiments, which determines how many and which FR

83 conjugation to FPs and combined nanoprobe-FP FRET sensing.

84 te-based sensor for CaMKII activity, FRESCA (FRET-based sensor for CaMKII activity).

85 We also present an equation derived from FRET and anisotropy equations which converts anisotropy

86 Moreover, time-gated FRET imaging with the Ln-dye FRET pairs efficiently supp

87 of RNA, the U2AF1 subunit stabilizes a high FRET value, which by structure-guided mutagenesis corres

88 ne approach, we find that using average homo-FRET rates (k(FRET)), average fluorescence lifetimes (ta

89 rophores that are indirectly excited by homo-FRET (r(ET)) do not compromise the accuracy of calculate

90 Here, we describe homo-FRET measurements by monitoring anisotropy changes in ph

91 anisotropy in the same specimen during homo-FRET as well as non-FRET conditions.

92 rk, we present an approach to study GFP homo-FRET via a combination of time-resolved fluorescence ani

93 allows experiments performed on a given homo-FRET pair to be more easily compared across different op

94 Here we introduce the use of homo-FRET (Forster resonance energy transfer between identica

95 ool for the study and interpretation of homo-FRET.

96 scent molecules with different spectra, homo-FRET can occur between fluorescent molecules of the same

97 e anisotropy is a popular tool to study homo-FRET of fluorescent proteins as an indicator of dimeriza

98 ypic Forster resonance energy transfer (homo-FRET), in which the emitted radiation is partially depol

99 Overall, we demonstrate how FRET-FLIM imaging technology can be used to show localis

100 g site-directed mutagenesis, immunoblotting, FRET, and proximity-ligation assays, we show that both L

101 ompounds, chloroxine and myricetin, increase FRET and inhibit [(3)H]ryanodine binding to RyR1 at nano

102 ABA rapidly increases FRET efficiency in N. benthamiana leaf cells and Arabido

103 xcellent spectral overlap with the interbase FRET acceptors qAnitro and tCnitro, and demonstrate that

104 Here single-molecule intermolecular FRET measurements of wild-type E-cadherin and cis-intera

105 Finally, using intermolecular FRET analysis, we demonstrate that SWG directly binds to

106 Intramolecular FRET analysis in living nematodes demonstrates that SYD-

107 -soluble) antenna followed by intramolecular-FRET/TBET energy transfers.

108 e find that using average homo-FRET rates (k(FRET)), average fluorescence lifetimes (tau), and averag

109 We characterize a new, to our knowledge, FRET standard formed by two enhanced GFPs (eGFPs) and a

110 -rich splice site, U2AF2 switches to a lower FRET value characteristic of an open, side-by-side arran

111 erous methods have been developed to measure FRET in cells.

112 Using fluorescence and UV melts, FRET, and an exonucleolytic decay assay we define a conc

113 esterase LAPD, and the cAMP biosensor mlCNBD-FRET to the cilium.

114 J synapsis by pol mu using a single molecule FRET (smFRET) assay where we can measure the duration of

115 uence using a combination of single molecule FRET and optical tweezers.

116 tion of these proteins using single molecule FRET and small angle X-ray scattering.

117 Here we use real time single molecule FRET experiments and crystallography to investigate the

118 e force spectroscopy (SMFS), single-molecule FRET (smFRET), and molecular dynamics (MD) simulations,

119 Using single-molecule FRET (smFRET), we show here that both Ku plus XRCC4:DNA

120 ysical approaches, including single-molecule FRET (smFRET)- and gel-based nuclease assays, we show th

121 Single-molecule FRET analysis reveals that the riboswitch exists in two

122 In this work, we used single-molecule FRET and biochemical techniques to demonstrate that Mg2+

123 exchange mass spectrometry, single-molecule FRET and molecular dynamics simulations to map the clien

124 Employing a single-molecule FRET assay to probe the folding status of reconstituted

125 Here, we used single-molecule FRET assays with a nanodisc membrane reconstitution syst

126 Here, we combine single-molecule FRET experiments and molecular dynamics studies to eluci

127 Single-molecule FRET experiments that observe end synapsis in real-time

128 Using single-molecule FRET investigations, we show that in the presence of cal

129 Here we applied single-molecule FRET methods to the Enterococcus faecalis (Efa) Cas1-Cas

130 Here, we use single-molecule FRET to derive a model that couples ATP hydrolysis-depen

131 Here we use single-molecule FRET to follow the postrecognition states of MutS and th

132 s closing." Here, we applied single-molecule FRET to measure distance changes associated with DNA bin

133 interaction parameters from single-molecule FRET trajectories.

134 ilayer electrophysiology and single-molecule FRET, to address the relationship between SNARE complex

135 73 distances collected using single-molecule FRET, we determined a novel solution structure of the si

136 Using single-molecule FRET, we discover novel dynamic behavior in the closed s

137 Interestingly using single-molecule FRET, we find that similar functional and conformational

138 Using single-molecule FRET, we unveil a previously unobserved extended 4WJ con

139 Here we performed single-molecule FRET-based DNA unwinding experiments using various combi

140 This assay monitors FRET between fluorescent proteins fused to the mutant AB

141 e ability of stagRFP to couple with multiple FRET partners, we develop a novel multiplex method to ex

142 orescence lifetime imaging (2pFLIM) with new FRET biosensors to chronically image in vivo signaling o

143 ame specimen during homo-FRET as well as non-FRET conditions.

144 quality estimate for judging the accuracy of FRET-derived structures as opposed to precision.

145 It takes advantage of FRET between a single fluorophore attached to a biomolec

146 findings will find use in the application of FRET and fluorescence correlation spectroscopy for the a

147 oss-correlation and facilitates comapping of FRET.

148 ophore dipoles, complicate interpretation of FRET data and have not been typically accounted for.

149 The occurrence of FRET mechanism is due to intermolecular hydrogen bonding

150 uantified and liposomes containing a pair of FRET fluorophores.

151 troponin C (TnC) protein fused to a pair of FRET fluorophores.

152 is paper presents a study of the response of FRET based DNA aptasensors in the intracellular environm

153 However, to overcome the sparsity of FRET experiments, they need to be combined with computer

154 To fill this gap, we used an assay based on FRET that exploits a HEK293T "biosensor" cell line stabl

155 we developed an analytical strategy based on FRET-fluorescence lifetime imaging (FLIM) and fluorescen

156 Alongside a primer on FRET basics, we provide guidelines for making experiment

157 -loading using FRET pairs exhibited not only FRET but also a J-aggregate red-shift (116 nm).

158 PP proteins exhibited Fpn co-localization or FRET.

159 Overall, our FRET-based HTS platform sets the stage to screen large c

160 Thus, our FRET-based nanoparticle biosensor enables detection of n

161 t underutilized method called photobleaching FRET (pbFRET), with the major difference being that the

162 The technique, photoswitching FRET (psFRET), is similar to an established but underuti

163 arable kinetics and dynamic range to the PKA FRET reporter, AKAR3EV.

164 Concurrent to our primary FRET assay, we also developed a high-throughput compatib

165 Thus, we propose FRET-based hysteresis analysis as an express method for

166 polytopic transmembrane proteins, proximity FRET, and rotational diffusion of fluorophore dipoles, c

167 f the FRET data to account for the proximity FRET effect occurring in confined two-dimensional enviro

168 l homogeneous signaling technique called QTR-FRET, which combine QRET technology and time-resolved Fo

169 The dual-parametric QTR-FRET technique enables the linking of guanine nucleotide

170 The study indicates that the QTR-FRET detection technique presented here can be readily a

171 eal-time reaction monitoring method, the QTR-FRET technique was also applied for G(i)alpha GTP-loadin

172 One of the most robust ways of quantifying FRET is to measure changes in the fluorescence lifetime

173 and we highlight the utility of quantitative FRET for probing multiple interactions in the plasma mem

174 otropy changes into a factor we call delta r FRET (drFRET).

175 g moiety to develop a lactate/pyruvate ratio FRET-based genetically encoded indicator, Lapronic.

176 RCA-FRET provides simple, rapid, sensitive, and specific qua

177 present an important proof of concept of RCA-FRET imaging with a strong potential to advance in situ

178 ficient FRET donor that supports red/far-red FRET biosensing.

179 We identified nine Hits that reduced FRET between Lifeact and ABD.

180 In a previous high-throughput time-resolved FRET (TR-FRET) screen, we identified a class of compound

181 tion, competition binding, and time-resolved FRET assays in whole cells.

182 Time-resolved FRET experiments revealed that R712G and F750L populate

183 Time-resolved FRET revealed that the structure of the pre- and post-po

184 olog, here we used competitive time-resolved FRET to sensitively and quantitatively characterize the

185 ric micropeptide species still showed robust FRET with SERCA, and there was a surprising positive cor

186 ty to the carboxyl-terminus produced similar FRET ratios.

187 e- and post-power-stroke states with similar FRET distance and distance distribution profiles.

188 a single excitation wavelength, and a single FRET pair allowed for a simultaneous quantification of m

189 vated CO(2) and MeJA, did not increase SNACS FRET ratios.

190 Upon injection at the one-cell stage, FRET nanoprobes can be imaged in developing zebrafish em

191 hrough the transition from dynamic to static FRET signals.

192 ell capture efficiency, we employ a one-step FRET-based biosensor which monitors the single cancer ce

193 We observed strong FRET between engineered tryptophans in the alphaE(C)/J a

194 ulk Rac1 activity assays and spatio-temporal FRET image analysis, the extracellular and cytoplasmic C

195 ular crowding sensor optimized for long-term FRET measurements, we show that crowding is rather stabl

196 HCR-TG-FRET provided washing-free nucleic acid quantification w

197 Cherry demonstrate the versatility of the TG-FRET nanoprobes and the possibility of in vivo bioconjug

198 -gated Forster resonance energy transfer (TG-FRET) between terbium donors and dye acceptors into HCR

199 donor fluorophore at its free end, such that FRET with acceptor fluorophores in the membrane provides

200 The FRET efficiency is modulated upon Ca(2+) ion binding.

201 The FRET in the solid-state coaxial heterojunctions with an

202 The FRET probes, with a FRET efficiency of ~20% at physiolog

203 eplacing Na(+) with Cs(+) does not alter the FRET efficiencies of the states significantly, but shift

204 An excellent agreement is found between the FRET efficiency calculated from the fit of the eGFP15eGF

205 We directly compared the FRET results with single-molecule mechanical events exam

206 discuss technical issues for converting the FRET-based cyclization/decyclization rates to an equilib

207 limit of detection was slightly higher, the FRET assay is superior for the detection of small vesicl

208 asein or E-cadherin as substrates and in the FRET peptide assay.

209 There was a significant reduction in the FRET signal obtained from analysis of murine TRPC6 FRET

210 After ligation, the FRET signal becomes static.

211 s, and we use Monte Carlo simulations of the FRET data to account for the proximity FRET effect occur

212 sm for the experimental determination of the FRET efficiency at high excitation intensity when satura

213 Before ligation, dynamic fluctuations of the FRET signal are observed due to transient binding of the

214 Taken together, the FRET assay is a simple, robust, and versatile method for

215 Using the FRET Hits, we show that our counter screen is sensitive

216 cell lactate and pyruvate dynamics using the FRET sensors Laconic and Pyronic.

217 When the FRET probe was expressed in human cells, both FRET effic

218 itro and tCnitro, and demonstrate that these FRET pairs enable conformation studies of DNA and RNA.

219 With these FRET reporters, we determined VRAC activation, non-invas

220 ial sensor was 10 CFU/ml and ability of this FRET immunosensor for Campylobacter jejuni sensing in co

221 We show that three FRET efficiencies and kinetic parameters can be determin

222 We describe a real-time FRET assay with a thioester linked E2~Ub conjugate to mo

223 TR-FRET resolved an equilibrium between two distinct struct

224 vious high-throughput time-resolved FRET (TR-FRET) screen, we identified a class of compounds that bi

225 etection, its inherent sensitivity (e.g., TR-FRET versus radiometric detection), and the ability to i

226 luorescent probes and used intramolecular TR-FRET to assess interlobe distances when CaM is bound to

227 identify IL-36 antagonists using a novel TR-FRET binding assay.

228 ce of enzymatic activity, increase in the TR-FRET signal between the biotin-bound Eu(III)-labeled str

229 solved Forster resonance energy transfer (TR-FRET) detection method for PTMs of cysteine residues usi

230 d fluorescence resonance energy transfer (TR-FRET) to study structural changes in CaM that may play a

231 solved Forster resonance energy transfer (TR-FRET).

232 Forster resonance energy transfer (FRET) and fluorescence cross-correlation spectroscopy ar

233 r, we use Forster resonance energy transfer (FRET) and fluorescence intensity fluctuation spectroscop

234 -molecule Forster Resonance Energy Transfer (FRET) and kinetic Monte Carlo (kMC) simulations.

235 nciple of Forster resonance energy transfer (FRET) and using upconversion nanoparticles (UCNPs) funct

236 Both fluorescence resonance energy transfer (FRET) and western blotting revealed the activation of Sr

237 mployed a Forster resonance energy transfer (FRET) approach using a small fluorescein arsenical hairp

238 ngineer a Forster resonance energy transfer (FRET) based biosensor deemed BioSTING.

239 tructed a Forster Resonance Energy Transfer (FRET) based pH nanoprobe using upconversion nanoparticle

240 We used Forster energy transfer (FRET) between 7AW and the flavin to estimate the distanc

241 show that Forster resonance energy transfer (FRET) between fluorescent dyes and between lanthanide (L

242 measured Forster resonance energy transfer (FRET) between fluorescent proteins fused to the C-termin

243 ng a fluorescence resonance energy transfer (FRET) biosensor-based assay, a variety of photopharmacol

244 robes and Forster resonance energy transfer (FRET) biosensors to monitor the changes in Ran and impor

245 ssays and Forster resonance energy transfer (FRET) distance measurements.

246 interbase Forster resonance energy transfer (FRET) donor.

247 ence in a Forster resonance energy transfer (FRET) donor/acceptor couple of antibody functionalized w

248 ied novel Forster resonance energy transfer (FRET) dual DNA probes with the excimer-forming pyrene pa

249 (FCS) and Forster resonance energy transfer (FRET) enable assessment of interaction between proteins.

250 itored by Forster resonance energy transfer (FRET) experiments both in solution and on surface-anchor

251 Fluorescence resonance energy transfer (FRET) experiments show that the mBBC formation is driven

252 ular fluorescence resonance energy transfer (FRET) experiments to determine structural changes of PLB

253 s exhibit Forster resonance energy transfer (FRET) from the PDHF inner core to the P3EHT outer core w

254 arably to Forster resonance energy transfer (FRET) has not yet been reported.

255 Forster resonance energy transfer (FRET) is a powerful tool to investigate the interaction

256 says, and Forster resonance energy transfer (FRET) measurements.

257 atly from Forster Resonance Energy Transfer (FRET) measurements.

258 py (FLIM)-Forster resonance energy transfer (FRET) microscopy data acquired in live cells coexpressin

259 with fluorescence resonance energy transfer (FRET) microscopy to uncover the molecular mechanism for

260 dot (QD) Forster resonance energy transfer (FRET) nanoprobe with narrow and tunable emission bands f

261 ovel fluorescence resonance energy transfer (FRET) peptide derived from a gel-based label-free proteo

262 ree-color Forster resonance energy transfer (FRET) spectroscopy for probing sub-millisecond conformat

263 antum-dot Forster Resonance Energy Transfer (FRET) strategy for transducing analyte recognition into

264 firmed by Forster resonance energy transfer (FRET) studies to show membrane blending and confocal mic

265 rement of Forster resonance energy transfer (FRET) to detect changes in biosensor conformation that a

266 molecule Forster resonance energy transfer (FRET) to determine the influence of wild-type or S34F-su

267 and fluorescence resonance energy transfer (FRET) to quantify micropeptide oligomerization and SERCA

268 efficient Forster Resonance Energy Transfer (FRET) to red fluorescent acceptor hybridized at the part

269 ements of Forster resonance energy transfer (FRET), and for quantification of protein-protein interac

270 based on Forster resonance energy transfer (FRET), which uses the principles of polymer physics to p

271 a tunable Forster resonance energy transfer (FRET)-based assay to detect triplex/H-DNA-destabilizing

272 y encoded Forster Resonance Energy Transfer (FRET)-based biosensors are powerful tools to illuminate

273 we used a Forster Resonance Energy Transfer (FRET)-based cGMP biosensor combined with scanning ion co

274 oolbox of Forster Resonance Energy Transfer (FRET)-based ERK biosensors by creating a series of impro

275 ed an NIR Forster resonance energy transfer (FRET)-based genetically encoded calcium indicator (iGECI

276 tilized a Forster resonance energy transfer (FRET)-based molecular tension sensor and live cell imagi

277 oded fluorescence resonance energy transfer (FRET)-based Pb(2+) biosensor, 'Met-lead 1.44 M1', with e

278 orescence/Forster resonance energy transfer (FRET)-based probes are capable of monitoring the dynamic

279 Using a Forster resonance energy transfer (FRET)-based screening strategy, we found that the orphan

280 re, a new Forster resonance energy transfer (FRET)-based sensor is integrated with an optical fiber t

281 sses in a Forster resonance energy transfer (FRET)-operated photochromic fluorene-dithienylethene dya

282 ple using Forster resonance energy transfer (FRET).

283 tudied by Forster resonance energy transfer (FRET).

284 e by fluorescence resonance energy transfer (FRET).

285 cule fluorescence resonance energy transfer (FRET).

286 bing fluorescence-resonance-energy-transfer (FRET) biosensor (FynSensor) that reveals cellular Fyn ac

287 ate-based Forster-resonance energy-transfer (FRET) method to investigate the release of novel high-dr

288 ignal obtained from analysis of murine TRPC6 FRET constructs with homologous amino-terminal mutations

289 Here, we present H-NE and H-CG, two FRET-based reporters armed with a DNA minor groove binde

290 patible counter screen to remove undesirable FRET Hits.

291 We then use FRET to analyze the dimerization of human rhomboid prote

292 Using FRET assays to monitor conformational changes of pol bet

293 Using FRET-cAMP nanorulers, we directly map cAMP gradients at

294 Using FRET-force biosensors for E-cadherin, we observed signif

295 Here, using FRET and fluorescence cross-correlation spectroscopy, we

296 ed nanoparticles with high dye-loading using FRET pairs exhibited not only FRET but also a J-aggregat

297 r direct detection of ascorbic acid (AA) via FRET quenched.

298 s in real-time at single-cell resolution via FRET.

299 nching of upconverted light from Au/UCNP via FRET after target (ochratoxin A, OTA) detection.

300 riments, which determines how many and which FRET pairs should be used to minimize the uncertainty an