ライフサイエンスコーパス: bimolecular

1 a host indole receptor may exhibit a unique bimolecular (2:1) binding stoichiometry not observed wit

2 alance between the unimolecular (A(AC)1) and bimolecular (A(AC)2) reaction pathways.

3 entration of the precursor, k(1obs) = k(1obs(bimolecular))[A].

4 ace growth, A + B --> 2B (rate constant k2), bimolecular agglomeration, B + B --> C (rate constant k3

5 on), (2) intramolecular aromatic ene and (3) bimolecular Alder ene.

6 e found that the mechanical stability of the bimolecular alphaIIbbeta3-ligand complexes had the follo

7 Bimolecular and Auger charge-carrier recombination rate

8 The results were compared with those for bimolecular and intramolecular Diels-Alder reactions in

9 the use of molecular cobaloxime catalysts in bimolecular and supramolecular photocatalysis schemes fo

10 the key catalyst decomposition pathways are bimolecular, and lowering the catalyst concentration oft

11 We estimate monomolecular lifetimes, bimolecular annihilation rate constants, and triplet exc

12 n forked DNA substrates up to 10-fold and on bimolecular anti-parallel G-quadruplex DNA structures an

13 This transformation is uniquely capable of bimolecular assembly of 2-siloxy-1,4-dienes and can be u

14 Furthermore, the rates of bimolecular association are very fast with k(on) approxi

15 When reconfiguration is fast, bimolecular association is not stable, but as reconfigur

16 ophobic residues on the same time scale that bimolecular association occurs, whereas the rabbit seque

17 .s)(-1), values that are similar to those of bimolecular association of small, complementary DNA stra

18 The bimolecular association rate is only weakly dependent on

19 )Ph2 with methyl propiolate], in line with a bimolecular associative transformation.

20 Supramolecular assembly 1 catalyzes a bimolecular aza-Prins cyclization featuring an unexpecte

21 an oligonucleotide-based probe, ratiometric bimolecular beacon (RBMB), which generates a detectable

22 ely 0.6 mg/mL fits well with an irreversible bimolecular binding model with the rate constant kon = (

23 luence of the 5' aptamer modification on the bimolecular binding rate constant kon and no significant

24 ngle-site bis-phosphonate catalysts and fast bimolecular bis-carboxylate catalysts, have reached turn

25 ractive vehicles for therapeutic delivery of bimolecular cargo such as nucleic acids, proteins, and e

26 lectric-field-induced reduction of radiative bimolecular carrier recombination together with motion o

27 bular macromolecule and its application as a bimolecular catalyst are reported.

28 tic site isolation in the MOF which prevents bimolecular catalyst deactivation pathways.

29 Single-site catalysts have an advantage over bimolecular catalysts because they remain effective when

30 f the Marcus inverted region in photoinduced bimolecular charge separation processes.

31 chromophore experiments such as photoinduced bimolecular charge transfer.

32 his article reviews progress in the study of bimolecular chemical reaction dynamics in solution, conc

33 ductions, autoxidation is now competing with bimolecular chemistry even in the most polluted North Am

34 ic photoassociation, Feshbach resonances and bimolecular collisions, these approaches have been limit

35 Bimolecular complementation assays showed that the TAD o

36 Here we use two independent bimolecular complementation assays, i.e. yeast two-hybri

37 VP16 interacted with cellular Mediator 25 in bimolecular complementation assays.

38 g bioluminescence resonance energy transfer, bimolecular complementation techniques, and cell-signali

39 Thus the LSP1-myosin1e bimolecular complex plays a pivotal role in the regulati

40 y ternary association of competitor with the bimolecular complex.

41 REB-binding protein (NCBD), along with their bimolecular complex.

42 eneral, accelerate the breakdown of isolated bimolecular complexes by occluding rapid rebinding of th

43 y informative to determine the structures of bimolecular complexes in solution.

44 ration and a new way, by sliding on DNA, for bimolecular complexes to form among proteins not involve

45 Bimolecular condensation reactions involving M2, M9, and

46 oduct of the combined process is formed by a bimolecular coupling of the two substrates activated by

47 ty by isolating the metal center, preventing bimolecular decomposition paths and facilitating product

48 on is either much faster or much slower than bimolecular diffusion, biomolecular association is not s

49 the structural features of its interface: a bimolecular domain formed by intertwining of the small d

50 f solute diffusion and solvation dynamics on bimolecular electron transfer in ionic liquids (ILs).

51 by some factor not properly accounted for in bimolecular electron transfer models based on a spherica

52 vary 1000-fold, enabling stringent tests of bimolecular electron transfer models.

53 ceptor state is predominantly deactivated by bimolecular electron transfer reactions (yielding radica

54 photovoltaics (OPVs) lead to a high rate of bimolecular encounters between spin-uncorrelated electro

55 and for ca. 1:1 mol:mol mixed valencies, the bimolecular ET rate constants (assuming a cubic lattice

56 he GPCR-G-protein interaction is viewed as a bimolecular event involving the formation of a ternary l

57 A bimolecular event occurring on the sensor area of the de

58 icting the outcome for the H + H2 --> H2 + H bimolecular exchange reaction that it might seem further

59 f granzyme and perforin acts as an effective bimolecular filter to ensure target specificity.

60 d, GST pull-down, co-immunoprecipitation and bimolecular florescence complementation, we found that S

61 ioluminescence resonance energy transfer and bimolecular fluorescence and bioluminescence complementa

62 bunits were observed in yeast two-hybrid and bimolecular fluorescence assays, consistent with a more

63 beta1-adrenoceptor homodimers constrained by bimolecular fluorescence complementation (9.8- and 9.9-f

64 rmed in the nucleus of living plant cells by bimolecular fluorescence complementation (BiFC) analyses

65 This method is based on bimolecular fluorescence complementation (BiFC) analysis

66 ays with electrophysiology and imaging-based bimolecular fluorescence complementation (BiFC) and biol

67 Bimolecular fluorescence complementation (BiFC) and co-i

68 ntification and tracking of hybrids based on bimolecular fluorescence complementation (BiFC) and foun

69 rtners in the RLR pathway through the use of bimolecular fluorescence complementation (BiFC) and supe

70 Over the last decade, bimolecular fluorescence complementation (BiFC) assay ha

71 The bimolecular fluorescence complementation (BiFC) assay ha

72 Here, we describe a bimolecular fluorescence complementation (BiFC) assay to

73 , protein coimmunoprecipitation (Co-IP), and bimolecular fluorescence complementation (BiFC) assays d

74 2 interacted using coimmunoprecipitation and bimolecular fluorescence complementation (BiFC) assays i

75 rescent resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC) assays r

76 Yeast two-hybrid screening combined with bimolecular fluorescence complementation (BiFC) experime

77 normal and mutant ZnTs, we applied here the bimolecular fluorescence complementation (BiFC) techniqu

78 present study, a genome-wide screen based on bimolecular fluorescence complementation (BiFC) was perf

79 Studies using coimmunoprecipitation (co-IP), bimolecular fluorescence complementation (BiFc), and col

80 of precisely defined GPCR dimers, trapped by bimolecular fluorescence complementation (BiFC).

81 ion of multiple normal and mutant ZnTs using bimolecular fluorescence complementation (BiFC).

82 d in heterologous systems, assays relying on bimolecular fluorescence complementation (BiFC; also ref

83 iction modeling of the complex structure and bimolecular fluorescence complementation analyses reveal

84 Bimolecular fluorescence complementation analyses showed

85 etween NPR3 and NPR1/TGA2 was explored using bimolecular fluorescence complementation analysis in oni

86 Interestingly, bimolecular fluorescence complementation analysis showed

87 Lastly, bimolecular fluorescence complementation analysis sugges

88 Bimolecular fluorescence complementation analysis to det

89 Using bimolecular fluorescence complementation analysis we sho

90 Using bimolecular fluorescence complementation analysis, we de

91 of the Bcl-2 family in living cells by using bimolecular fluorescence complementation analysis.

92 PYL6 and MYC2 interact in planta based on bimolecular fluorescence complementation and co-immunopr

93 family encoding CAR1 to CAR10 proteins, and bimolecular fluorescence complementation and coimmunopre

94 us and interact with each other in planta in bimolecular fluorescence complementation and coimmunopre

95 We investigated the topology of Toc75 using bimolecular fluorescence complementation and immunogold

96 Using bimolecular fluorescence complementation and metabolic l

97 Here we develop a new method combining bimolecular fluorescence complementation and photoactiva

98 Analysis by bimolecular fluorescence complementation and yeast-two-h

99 Bimolecular fluorescence complementation assay confirms

100 action spectrum of HDC1 using a quantitative bimolecular fluorescence complementation assay in tobacc

101 Furthermore, bimolecular fluorescence complementation assay shows tha

102 We created a bimolecular fluorescence complementation assay to detect

103 Using a Bimolecular Fluorescence Complementation assay, we have

104 Using a validated bimolecular fluorescence complementation assay, we provi

105 f with Tec family kinases using a cell-based bimolecular fluorescence complementation assay.

106 tion in ABT-263-treated cells, shown using a bimolecular fluorescence complementation assay.

107 supported by its interaction with RIP1 in a bimolecular fluorescence complementation assay.

108 Bimolecular fluorescence complementation assays confirm

109 In planta bimolecular fluorescence complementation assays confirme

110 Bimolecular fluorescence complementation assays indicate

111 Bimolecular fluorescence complementation assays reveal a

112 Bimolecular fluorescence complementation assays reveal P

113 Both yeast two-hybrid and bimolecular fluorescence complementation assays were use

114 st (Saccharomyces cerevisiae) two-hybrid and bimolecular fluorescence complementation assays, HSFA4A

115 Using biochemical, pharmacological, and Bimolecular Fluorescence Complementation assays, we have

116 Using the yeast two-hybrid system and bimolecular fluorescence complementation assays, we show

117 by yeast two-hybrid, in vitro pulldown, and bimolecular fluorescence complementation assays.

118 co-immunoprecipitation, co-localization and bimolecular fluorescence complementation assays.

119 ybrid tests, immuno-pull-down assays, and by bimolecular fluorescence complementation at the apical p

120 Co-localization of Pi04089 and StKRBP1, and bimolecular fluorescence complementation between them, i

121 In vivo interaction studies using bimolecular fluorescence complementation between VSR2;1,

122 Bimolecular Fluorescence Complementation demonstrated th

123 Yeast two-hybrid and bimolecular fluorescence complementation experiments fur

124 Bimolecular fluorescence complementation experiments in

125 Furthermore, yeast two-hybrid and bimolecular fluorescence complementation experiments sug

126 abidopsis thaliana mesophyll protoplasts and bimolecular fluorescence complementation in living PTs.

127 This observation was confirmed by bimolecular fluorescence complementation in planta.

128 pha in N. benthamiana, which was detected by bimolecular fluorescence complementation in the nucleopl

129 le of in vitro binding to, and shows in vivo bimolecular fluorescence complementation interaction in

130 Bimolecular fluorescence complementation of the N- and C

131 Bimolecular fluorescence complementation results indicat

132 Bimolecular fluorescence complementation reveals that th

133 Co-immunoprecipitation and bimolecular fluorescence complementation studies showed

134 The bimolecular fluorescence complementation studies showed

135 Bimolecular fluorescence complementation studies suggest

136 t in transgenic Nicotiana benthamiana cells, bimolecular fluorescence complementation suggested that

137 monstrated by both coimmunoprecipitation and bimolecular fluorescence complementation that these NF-Y

138 We conducted coimmunoprecipitation and bimolecular fluorescence complementation to determine th

139 ioluminescence resonance energy transfer and bimolecular fluorescence complementation to establish th

140 We used bimolecular fluorescence complementation to show that ex

141 Here we utilized indirect bimolecular fluorescence complementation to visualize a

142 Bimolecular fluorescence complementation was used to stu

143 Here, we used the BiFC (bimolecular fluorescence complementation) assay and repo

144 Small RNA analysis, bimolecular fluorescence complementation, and coimmunopr

145 Co-immunoprecipitation, colocalization, bimolecular fluorescence complementation, and mutational

146 , they were recovered in vivo by ratiometric bimolecular fluorescence complementation, and they were

147 In vitro pull-down, bimolecular fluorescence complementation, coimmunoprecip

148 In vitro pull-down, bimolecular fluorescence complementation, coimmunoprecip

149 Bimolecular fluorescence complementation, Forster resona

150 dimers was shown to occur in plant cells by bimolecular fluorescence complementation, pointing to th

151 yeast (Saccharomyces cerevisiae NMY51), and bimolecular fluorescence complementation, to show that,

152 nally, using both co-immunoprecipitation and bimolecular fluorescence complementation, we demonstrate

153 Using bimolecular fluorescence complementation, we observed th

154 Moreover, using photoconvertible bimolecular fluorescence complementation, we selectively

155 leaching at variable radius experiments with bimolecular fluorescence complementation, we show that t

156 Here, we used a Bimolecular Fluorescence Complementation-based functiona

157 ivity, Torso dimerization was detected using bimolecular fluorescence complementation.

158 a dimers at the plasma membrane in planta by bimolecular fluorescence complementation.

159 d on a yeast two-hybrid screen and in planta bimolecular fluorescence complementation.

160 the interaction was found in the nucleus by bimolecular fluorescence complementation.

161 1 self-association also occurs in vivo using bimolecular fluorescence complementation.

162 cells by immunofluorescence microscopy using Bimolecular Fluorescence Complementation.

163 wn with CaM Sepharose, CaM overlay assay and bimolecular fluorescence complementation.

164 Using in vivo bimolecular fluorescent complementation (BiFC) assays, w

165 (Saccharomyces cerevisiae) three-hybrid and bimolecular fluorescent complementation assays revealed

166 Yeast two-hybrid, coimmunoprecipitation and bimolecular fluorescent complementation assays showed th

167 Yeast- or protoplast-based two-hybrid and bimolecular fluorescent complementation assays showed th

168 of the Ba, the recombination shifts towards bimolecular from monomolecular.

169 synthesized for the very first time via the bimolecular gas-phase reaction of ground-state carbon at

170 Such bimolecular indole-mediated activation of the human AHR

171 inhibited African malaria mosquito AChE with bimolecular inhibition rate constants (k(inact)/K(I)) of

172 27-264 binds to DeltaF508-CFTR, suggesting a bimolecular interaction.

173 The standard description of bimolecular interactions posits that TF off rates are in

174 f 600-750 pN, making it one of the strongest bimolecular interactions reported, equivalent to half th

175 internal forces are generated affecting the bimolecular interactions that maintain cell-cell adhesio

176 new strategy to characterize the response of bimolecular interactions to forces even in the presence

177 y a two-step process, which consists of fast bimolecular intercalation of the first dppz moiety follo

178 ucidated in detail for several examples, the bimolecular intermolecular coupling could not be assigne

179 rate constants for intracomplex (k(et)) and bimolecular (k(2)) ET.

180 f two inhibitory sites on open channels with bimolecular kinetics.

181 long-lived nonconducting events that follow bimolecular kinetics.

182 ction rate (1.43 x 10(5) s(-1)) than that of bimolecular Langmuir-Hinshelwood (L-H) pathway (4.29 s(-

183 eta hydroxy peroxy radicals depends on their bimolecular lifetime (taubimolecular).

184 iving cells using a new recombinase enhanced bimolecular luciferase complementation platform (ReBiL).

185 re we developed a highly specific and robust bimolecular luminescence complementation (BiLC) reporter

186 revealed that these reactions proceed via a bimolecular mechanism in which either the basic Al(I) ce

187 tem that can undergo glycosylation through a bimolecular mechanism.

188 uct is then oxidized by the ferrocenium in a bimolecular MS-CPET step.

189 Eyring analysis is consistent with the bimolecular nature of the reaction, with DeltaH(double d

190 ults obtained definitively rule out a simple bimolecular nucleation mechanism and provide evidence fo

191 ntimate mechanisms of nucleation are tested: bimolecular nucleation, termolecular nucleation, and a m

192 s of the stannane cation radicals occur by a bimolecular, nucleophile-assisted mechanism (S(N)2).

193 Bimolecular nucleophilic addition generates bent 1,3-zwi

194 roton source in a rare example of asymmetric bimolecular nucleophilic addition into an oxocarbenium i

195 Terminating the process through bimolecular nucleophilic addition into the intermediate

196 cks of enzyme chemistry: "Proton transfer," "Bimolecular nucleophilic addition," "Bimolecular nucleop

197 The competition between bimolecular nucleophilic substitution and base-induced e

198 ause the key bond-forming step proceeds in a bimolecular nucleophilic substitution fashion.

199 The SN2 reaction (bimolecular nucleophilic substitution) is a well-known c

200 sfer," "Bimolecular nucleophilic addition," "Bimolecular nucleophilic substitution," and "Unimolecula

201 oncepts needed to understand two-dimensional bimolecular organizations at the vacuum-solid interface.

202 change and a pseudo-free energy penalty for bimolecular pairing of nucleotides that are unlikely to

203 probabilities, is applied per nucleotide in bimolecular pairs, and this approach is able to predict

204 ps and their precise chemical descriptors of bimolecular particle agglomeration, B + B --> C, and aut

205 A bimolecular pathway involving hydrogen-atom-transfer fro

206 Bimolecular pathways were invoked in early proposals, bu

207 Bimolecular peroxy decomposition is promoted by the red-

208 These results suggest that bimolecular phenoxy radical couplings in nature can be c

209 the formation of excited ions upon ultrafast bimolecular photoinduced charge separation is found usin

210 intrinsic, diffusion free, rate constant of bimolecular photoinduced electron transfer reactions, fl

211 The dynamics of bimolecular photoinduced electron-transfer reactions has

212 understanding of the dynamics of elementary (bimolecular) polyatomic reactions in the gas-phase have

213 ization of nitrones proceeds via a diradical bimolecular process involving an initial dimerization th

214 Kinetic studies indicate a bimolecular process, rate = k [Fe(NO)2](1)[CO](1), and a

215 the addition of H2 to triphosphabenzene is a bimolecular process.

216 Unimolecular and bimolecular processes have also been considered.

217 Several bimolecular processes involving an initial dimerization

218 ationalized as an interplay between uni- and bimolecular processes.

219 hich phosphoryl transfer through a series of bimolecular protein-protein interactions is coupled to s

220 However, bimolecular protonation by a proton donor from the bulk

221 arent Stern-Volmer (KsvApp) and the apparent bimolecular quenching constants (kqApp) were calculated

222 The synthesis features a bimolecular radical addition/cyclization/fragmentation c

223 emperature and pressure, identifying the key bimolecular radical reactions responsible for the low ac

224 elative rate techniques were used to measure bimolecular rate coefficients for reactions of EtFBA wit

225 C-LR followed second-order kinetics with the bimolecular rate constant (kMCLR+Fe(VI)) decreasing from

226 The bimolecular rate constant for reaction of alanine with O

227 y generated Ru(bpy)3(3+) and 1 occurs with a bimolecular rate constant of 2.5 x 10(8) M(-1) s(-1).

228 ropane-fused trans-cyclooctene (sTCO) with a bimolecular rate constant of 72,500 +/- 1660 M(-1) s(-1)

229 The bimolecular rate constant of HNO with PY in pH 7.4 phosp

230 The enzymes show apparent bimolecular rate constants and deuterium kinetic isotope

231 Bimolecular rate constants for association are weakly se

232 Near room temperature, in dry samples, bimolecular rate constants for ET between organothiolate

233 Bimolecular rate constants for the reaction of STAR with

234 the ferrocene derivative, as expected, with bimolecular rate constants in the range 10(3)-10(5) M(-1

235 ) </= 12.7 protonate [Fe2(bdt)(CO)6](-) with bimolecular rate constants of 4 x 10(6), 7 x 10(6), and

236 Moreover, apparent bimolecular rate constants of the reaction of compound I

237 ively, affording 5-fluoro-1,4-pyrazoles with bimolecular rate constants up to 10(4) m(-1) s(-1) , sur

238 We present all relevant apparent bimolecular rate constants, the spectral signatures of t

239 NH2OH, forming the N-N bond of N2O during a bimolecular, rate-determining step.

240 On the other hand, considering a fast bimolecular reaction A + B --> C occurring as A displace

241 ed for Phi-value analysis has now revealed a bimolecular reaction hidden beneath the observed first-o

242 We are not aware of any single-step, bimolecular reaction in which two hydrogen atoms are sim

243 This transformation exhibits bimolecular reaction kinetics and represents a key step

244 age of the Maillard reaction by a reversible bimolecular reaction mechanism and also to evaluate the

245 A bimolecular reaction mechanism involving a Mn(IV)-hydrox

246 ron molecule (HCCBS) has been formed via the bimolecular reaction of the boron monosulfide radical (B

247 e) was synthesized for the first time by the bimolecular reaction of the simplest silicon-bearing rad

248 ution, respectively, which demonstrates that bimolecular reaction rate coefficients can be quantified

249 Bimolecular reaction rate constants with hydroxyl radica

250 Bimolecular reaction rates are at least an order of magn

251 , whereas thermal reaction of 1a proceeds by bimolecular reaction with the substrate.

252 reacts with the probe via an unaccelerated, bimolecular reaction.

253 ksi values of 5 and 300 m(3)/s.mol for these bimolecular reactions at defective and pristine sites, r

254 We show that bimolecular reactions between species confined to the su

255 demonstrate that the key dynamics of complex bimolecular reactions can be captured with a relatively

256 obtained using known bulk-phase kinetics for bimolecular reactions in our colliding-droplet microreac

257 tion in the gas phase to a series of radical bimolecular reactions in the condensed phase.

258 n of the oxidized molecular catalyst 1(+) in bimolecular reactions is also evidenced for the first ti

259 usion of the reactants on the time course of bimolecular reactions is to modify or renormalize the ph

260 nderstand the key reactivity determinants of bimolecular reactions of Criegee intermediates and H2 X

261 We thoroughly discuss bimolecular reactions of PBDEs with Br and H, as well as

262 Polar bimolecular reactions often begin as charge-transfer com

263 Importantly, for bimolecular reactions we derive an exact expression rela

264 At low concentrations, solution bimolecular reactions will be relatively less important

265 recycle these catalysts but also to minimize bimolecular reactions with ethyl diazoacetate.

266 Unimolecular isomerization and bimolecular reactions with organic peroxy radicals are a

267 cs by controlling the rates of diffusion and bimolecular reactions within the cell interior.

268 For bimolecular reactions, the activation energies are the s

269 including the transition state for activated bimolecular reactions.

270 rs 2-T and 4-T decayed by competing uni- and bimolecular reactions.

271 peroxy radicals lose O2 in competition with bimolecular reactions.

272 tanding quantum state resolved reactivity in bimolecular reactions.

273 An example is bimolecular reactivity of complementary-functionalized p

274 s that exploit the remarkable specificity of bimolecular recognition, i.e., of both G proteins and RT

275 Due to the large electron-hole bimolecular recombination associated with tin and the re

276 The bimolecular recombination coefficient (10(-11) to 10(-10

277 ime, which correlates to a smaller radiative bimolecular recombination coefficient.

278 Bimolecular recombination dominates in materials where t

279 arges measured via their intensity-dependent bimolecular recombination dynamics at room temperature.

280 ng photoluminescence studies, that radiative bimolecular recombination is dominant at higher excitati

281 While the reduced bimolecular recombination with raising fluorine concentr

282 observe the formation of T1 states following bimolecular recombination, indicating that encounters of

283 cation of spectral features while minimizing bimolecular recombination.

284 dyl ligand is found to enhance the rate of a bimolecular reduction mechanism of CO2 by Re(I) fac-tric

285 One of those pathways is a bimolecular reductive coupling via intermediate (N^O)Ni(

286 mplexes that allow the direct observation of bimolecular reductive elimination to generate ethane and

287 ms were developed for improved prediction of bimolecular RNA structure that consider the competition

288 A benchmark set of 17 bimolecular RNA structures was assembled to assess struc

289 These bimolecular roaming reactions are closely related to the

290 Bimolecular secondary structure prediction is also provi

291 perimental and theoretical results support a bimolecular sigma-bond metathesis mechanism in which the

292 ynamics simulation studies are described for bimolecular SN2 nucleophilic substitution, unimolecular

293 of the competition between unimolecular and bimolecular structure.

294 tides that are unlikely to be accessible for bimolecular structure.

295 r the competition between self-structure and bimolecular structure.

296 An on-surface bimolecular system is described, comprising a simple div

297 rogen migration of peroxy radicals and their bimolecular termination reactions.

298 anism compared to the solution analogue from bimolecular to single-site.

299 rier mobility, the IQE increases to 65%, but bimolecular triplet formation significantly increases an

300 IQE is 48% and 16% of excitations decay via bimolecular triplet formation.