ライフサイエンスコーパス: rotary

1 Revved-up rotary: A molecular Wankel motor, the dual-ring structur

2 We also observed a rotary action in the suspended supercooled drop driven b

3 Unique elastomeric rotary actuators based on pneumatically driven peristalt

4 Here we show that rotary adenosine triphosphatases (ATPases)/synthases fro

5 Solid-liquid extraction assisted by rotary agitator was utilised, using a mixture of methano

6 population lives within 2 hours by ground or rotary air transport of a verified burn center; however,

7 to verified burn centers by both ground and rotary air transport.

8 shows that the couplings underlie both ring rotary and bending motions.

9 ere we describe chemically-driven artificial rotary and linear molecular motors that operate through

10 They generate rotary and piston-like linear motion using specially des

11 t subunit H inhibits free V1 by bridging the rotary and stator domains.

12 The rotary arm with its azaterpyridine terminal is intramole

13 ectrochemical ion gradient is harnessed by a rotary ATP synthase to phosphorylate adenosine diphospha

14 Using a rotary ATPase as a working example, we show how this ass

15 For the first time in this rotary ATPase subtype, the peripheral stalk is resolved

16 model for the membrane-embedded motor of any rotary ATPase.

17 n the map, providing a complete model of the rotary ATPase.

18 All rotary ATPases catalyse the interconversion of ATP and A

19 Rotary ATPases couple ATP synthesis or hydrolysis to pro

20 ests that the mechanism of ATP generation by rotary ATPases is less strictly conserved than has been

21 Rotary ATPases play fundamental roles in energy conversi

22 the membrane, a feature now synonymous with rotary ATPases.

23 ion between the compartmentalized two-sector rotary ATPases.

24 common mechanism for proton transport in all rotary ATPases.

25 ust; Prince Charles Hospital Foundation; and Rotary Australia.

26 Rotary biomolecular machines rely on highly symmetric su

27 sed chemomechanical group transfer theory of rotary biomolecular motors is applied to treat single-mo

28 e instrumental in energy conservation during rotary catalysis by the synthase.

29 Although the binding change mechanism of rotary catalysis by which F1-ATPase hydrolyzes ATP has b

30 g local field that generates torque to drive rotary catalysis in F(1).

31 Rotary catalysis in F(1)F(0) ATP synthase is powered by

32 Rotary catalysis in F1F0 ATP synthase is powered by prot

33 ur results identify the common properties of rotary catalysis of V1-ATPases that are distinct from th

34 istinct regulatory interactions with F1 when rotary catalysis operates in opposite directions for the

35 ATP synthases produce ATP by rotary catalysis, powered by the electrochemical proton

36 drolysis and serves an essential function in rotary catalysis.

37 into the conformational changes implicit in rotary catalysis.

38 ave been arrested at the same point in their rotary catalytic cycles.

39 Hereunto, the workflow of two multicomponent rotary catalytic machineries was interlinked by the simu

40 talytic sites, details directly supporting a rotary catalytic mechanism analogous to that of the hete

41 ATP synthases operate by a rotary catalytic mechanism where proton translocation th

42 microgravity (muXg) using the NASA developed rotary cell culture system (RCCS) enhanced bone resorbin

43 study, DC were cultured from 2-14 days in a rotary cell culture system, which generates a simulated

44 tudy was to investigate the potential use of rotary cell culture systems (RCCS) as a means to enhance

45 A versatile Rotary Chemical Vapour Deposition (RCVD) technique for t

46 of the challenge involves understanding the rotary-chemical coupling by a nonphenomenological struct

47 experimental findings and indicate that the rotary-chemical coupling is primarily established throug

48 structure-based free energy landscape of the rotary-chemical process.

49 he peripheral V1 domain drives rotation of a rotary complex (the rotor) relative to the stationary pa

50 ibration-suppressing platforms, supports for rotary components, machine tool mounts and metrology fra

51 Cy3 DIGE and detected simultaneously with a rotary confocal fluorescence scanner.

52 led channels, and detected with a four-color rotary confocal fluorescence scanner.

53 tercurrent chromatography (HSCCC), low-speed rotary countercurrent chromatography (LSRCCC) and spiral

54 Our understanding of the rotary-coupling mechanism of F(1)-ATPase has been greatl

55 F1-ATPase inhibitor protein, IF1, halts the rotary cycle at the catalytic dwell.

56 overcrowded alkenes is well established, but rotary cycles based purely on photochemical isomerizatio

57 anisms associated with spray production from rotary dental instrumentation with particular focus on w

58 mic force microscopy to demonstrate that the rotary device is fully functional after insertion.

59 res that emulate the elements of macroscopic rotary devices, such as those found in macroscopic gyros

60 time scale, which has contributions from the rotary diffusion of the protein, from internal motions i

61 equence independent, as is that from protein rotary diffusion.

62 type of wavemeter by exploiting its optical rotary dispersion.

63 by demonstrating a robust sequence-dependent rotary DNA device operating in a four-step cycle.

64 pecially when a single needle is inserted by rotary drilling and then retracted part way before infus

65 n was controlled by inserting needles with a rotary drilling device, which enabled localized injectio

66 hods of drying, hot air and microwaving with rotary drum, combined with quantitative Raman spectrosco

67 Here, we characterized the rotary dynamics of EhV1 using single-molecule analysis e

68 A suitable choice of rotary-echo parameters compensates for different scenari

69 he sensor spin by a composite pulse known as rotary-echo yields a flexible magnetometry scheme, mitig

70 The flagellum, a rotary engine required for motility in many bacteria, pl

71 carboxyfluorescein for vesicles prepared by rotary evaporation and found oligolamellar vesicles have

72 he Bangham thin-film hydration (conventional rotary evaporation method and using organic solvents) an

73 tion instead of more time and work consuming rotary evaporation.

74 The extracts were concentrated by rotary-evaporation and derivatized; no clean-up was nece

75 ation efficiency using both NanoAssemblr and rotary evaporator manufacturing processes.

76 ere extracted in cold acetone and dried in a rotary evaporator.

77 otors are not interfering and preserve their rotary function on gold.

78 interconversion may not be necessary during rotary function.

79 chemically treated with PVC in a bench-scale rotary furnace in order to remove heavy metals via the c

80 mycobacterium-specific loop of the enzyme's rotary gamma subunit plays a role in the coupling of ATP

81 )F(o) ATP synthase functions as a biological rotary generator that makes a major contribution to cell

82 esults imply that the motor's gait follows a rotary hand-over-hand mechanism.

83 vot point that appear suitable to coordinate rotary handoffs of kinked DNA intermediates among enzyme

84 Rotary has already transitioned its grants program to in

85 Rotary has contributed more than $1.61 billion for the g

86 mice is caused by loss of sensory input for rotary head movements (detected by cristae ampullaris) a

87 probe contained in a custom-built 3D-printed rotary holder.

88 A two-loop, eight-port rotary injection valve demonstrated better consistency o

89 th a heated single-pass spray chamber, and a rotary injection valve, used as an online interface betw

90 uctured sprays were produced by water-cooled rotary instruments, which, in the worst case of an air t

91 p among the World Health Organization (WHO), Rotary International, the Centers for Disease Control an

92 Rotary is providing additional support for routine immun

93 rent innovations in excitation laser source, rotary joint assembly, 1 mm IVPA-US catheter size, diffe

94 xty-three patients with subacute and chronic rotary knee joint trauma of either the left or right kne

95 ght to evaluate the use of a continuous-flow rotary left ventricular assist device (LVAD) as a bridge

96 LVAD device malfunctions (DMs) occurring in rotary LVADs implanted at a single center between April

97 Continuous-flow rotary LVADs represent an innovative design with potenti

98 The flagellar motor is a sophisticated rotary machine facilitating locomotion and signal transd

99 esting insight but could not account for the rotary mechanism by a nonphenomenological structure/ener

100 These results lead us to propose a rotary mechanism for ATR function in which, at any given

101 -molecule experiments and support a tri-site rotary mechanism for F(1)-ATPase under physiological con

102 ransmembrane proton pump that operates via a rotary mechanism fuelled by ATP.

103 ATP-dependent proton pumps that operate by a rotary mechanism in which ATP hydrolysis drives rotation

104 Sequence conservation indicates this rotary mechanism is fully possible for all eukaryotes an

105 les, and experimentally demonstrate that the rotary mechanism of its ATP synthase is coupled to the c

106 o this interface, which is essential for the rotary mechanism of the enzyme, appears to consist of he

107 s, these membrane-associated complexes use a rotary mechanism powered by the transmembrane diffusion

108 transient storage of energy required by the rotary mechanism takes place in the central stalk or in

109 ATP synthase uses a rotary mechanism to carry out its cellular function of m

110 ATP synthase uses a unique rotary mechanism to couple ATP synthesis and hydrolysis

111 ATP synthase uses a rotary mechanism to couple transmembrane proton transloc

112 upled to membrane-bound proton pump Vo via a rotary mechanism.

113 F(1)F(o) ATP synthases function by a rotary mechanism.

114 lated family of F1F0 ATP synthases, employ a rotary mechanism.

115 detailed understanding of the nature of its rotary mechanism.

116 inear response approximation to describe the rotary mechanism.

117 ue-speed curve at various [ATP]s and discuss rotary models in which the archaellum has characteristic

118 of funneling the photon energy into specific rotary modes, thus achieving photoisomerization quantum

119 cuolar H+-ATPase (V-ATPase) is an ATP-driven rotary molecular motor that is a transmembrane proton pu

120 directional rotation of [2]- and [3]catenane rotary molecular motors and the transport of substrates

121 The linear and rotary molecular motors are driven by aliquots of a chem

122 Unidirectional rotary molecular motors based on chiral overcrowded alke

123 Of particular interest are unidirectional rotary molecular motors driven by chemical fuel or light

124 The two opposed rotary molecular motors of the F0F1-ATP synthase work to

125 Previously, rotary molecular motors powered by light and chemical en

126 Synthetic light-driven rotary molecular motors show complicated structural dyna

127 V-ATPases are rotary molecular motors that generally function as proto

128 ndings will be essential in designing future rotary molecular motors.

129 r understanding of the general mechanisms of rotary molecular motors.

130 electron transport chain is harnessed by the rotary molecular nanomotor ATP synthase to generate ATP.

131 Rotary motion around a molecular axis has been controlle

132 dergo repetitive light-driven unidirectional rotary motion around the central C horizontal lineC bond

133 uch an analysis reveals how the character of rotary motion could be changed from a precessional motio

134 Subjects reported seeing rotary motion during viewing of all stimuli.

135 unit a in promoting proton translocation and rotary motion in the Escherichia coli F1Fo ATP synthase

136 his indicates that the ability to respond to rotary motion is more sensitive to the effects of aging.

137 ers have taken the approach of mimicking the rotary motion of helical bacterial flagella for propulsi

138 and cD61, and behaves as a leash that allows rotary motion of the c-ring to a limit of approximately

139 in promoting H(+) transport and the coupled rotary motion of the subunit c ring in F(1)F(0)-ATP synt

140 le in promoting H+ transport and the coupled rotary motion of the subunit c ring in F1F0-ATP synthase

141 key role in promoting H(+) transport-coupled rotary motion of the subunit c ring in F1Fo ATP synthase

142 owed significant enhancement if the flagella rotary motion was paralyzed.

143 Their rotary motion was studied by (1)H NMR and UV-vis absorpt

144 ed is the effect of solvent viscosity on the rotary motion when long, rigid substituents are present.

145 te state following the 40 degrees substep of rotary motion, and to study the timing and molecular mec

146 rvesting low-energy green light to power the rotary motion.

147 tor CheY plays a key role in regulating this rotary motion.

148 zed molecular machines based on light-driven rotary motion.

149 ors, and explains the stepped unidirectional rotary motion.

150 In particular, it lacked the necessary rotary motions in its limbs to push the body off the gro

151 e (F1-ATPase) can function as an ATP-fuelled rotary motor and has been integrated into self-assembled

152 l evolution of the prototypical light-driven rotary motor are followed on the ultrafast time scale by

153 Escherichia coli cells have a reversible rotary motor at the base of each filament.

154 This rotary motor catalyzes the synthesis of ATP with high ef

155 rchaellum (archaeal flagellum), a reversible rotary motor consisting of a torque-generating motor and

156 The rotary motor enzyme FoF1-ATP synthase uses the proton-mo

157 The vacuolar H(+)-ATPase (V-ATPase) is a rotary motor enzyme that acidifies intracellular organel

158 erial flagella are driven at their base by a rotary motor fueled by the membrane gradient of protons

159 Physiological properties of the flagellar rotary motor have been taken to indicate a tightly coupl

160 F1-ATPase is an ATP-driven rotary motor in which a rod-shaped gamma subunit rotates

161 herichia coli, the behavior of the flagellar rotary motor near zero load can be studied by scattering

162 e cell's inner membrane powers the flagellar rotary motor of Escherichia coli.

163 ical filaments, each driven at its base by a rotary motor powered by a proton or a sodium ion electro

164 is the catalytic portion of ATP synthase, a rotary motor protein that couples proton gradients to AT

165 is is the first example in which a molecular rotary motor shows self-assembly in an aqueous medium wi

166 The flagellum is a rotary motor that enables bacteria to swim in liquids an

167 The bacterial flagellar motor (BFM) is the rotary motor that rotates each bacterial flagellum, powe

168 tein complex that functions as an ion-driven rotary motor to propel cells through liquid media.

169 The universal joint or hook that links the rotary motor to the filament is composed of approximatel

170 binds to and locks the axle of the V-ATPase rotary motor would need to be re-evaluated.

171 flagellum is a motile organelle driven by a rotary motor, and its axial portions function as a drive

172 V-ATPase is a rotary motor, and recent structural analyses have reveal

173 synthase of Escherichia coli functions as a rotary motor, coupling the transmembrane movement of pro

174 eed of an overcrowded alkene-based molecular rotary motor, having an integrated 4,5-diazafluorenyl co

175 nts, each driven at its base by a reversible rotary motor, powered by a transmembrane proton flux.

176 nts, each driven at its base by a reversible rotary motor, powered by an ion flux.

177 1) portion, called F(1)-ATPase, can act as a rotary motor, with ATP binding, hydrolysis, and product

178 s into the molecular nature of the F1-ATPase rotary motor.

179 mparable to those generated by the flagellar rotary motor.

180 iven gamma-subunit rotation in the F1-ATPase rotary motor.

181 hine synthesizing or hydrolyzing ATP using a rotary motor.

182 nts, each driven at its base by a reversible rotary motor.

183 propelled by flagellar filaments driven by a rotary motor.

184 f these is F(o)F1-ATP synthase, the smallest rotary motor.

185 f up to 87% of crown ethers in a [2]catenane rotary motor.

186 ibe the origins of the first light-activated rotary motors and their modes of function, the structura

187 Molecular rotary motors based on oxindole which can be driven by v

188 ATP synthase contains two rotary motors coupled back-to-back: the protonmotive for

189 , the design of light-driven single molecule rotary motors has been mainly guided by the modification

190 y for the coupled rotations of the Fo and F1 rotary motors in ATP synthase, and explain the need for

191 l alkenes is the driving force for molecular rotary motors in nanoscale machines.

192 he bacterial flagellar motor, one of the few rotary motors in nature, produces torque to drive the fl

193 f model organic chromophores and synthesized rotary motors is used for rationalizing the effect of el

194 echanism of energy conversion in the coupled rotary motors of FoF1-ATP synthase.

195 directional rotation of individual molecular rotary motors on a quartz surface in unprecedented detai

196 Now, there are three rotary motors powered by protonmotive force: the bacteri

197 ynthases from coupling membranes are complex rotary motors that convert the energy of proton gradient

198 Unidirectional molecular rotary motors that harness photoinduced cis-trans (E-Z)

199 Driving molecular rotary motors using visible light (530-550 nm) instead o

200 e catalyzes the synthesis of ATP via coupled rotary motors within F0 and F1.

201 unifies the physical concepts of linear and rotary motors, and explains the stepped unidirectional r

202 ATPase is composed of two rotary motors, F0 and F1, which compete for control of t

203 n rotational mechanism for A-type and F-type rotary motors, in which the angular velocity is limited

204 Proton pumping is achieved by means of rotary motors, namely vacuolar ATPases (V-ATPase), which

205 esis of rotaxanes and catenanes to molecular rotary motors, shuttles, muscles, and other devices.

206 Although chemists have made small-molecule rotary motors, to date there have been no reports of sma

207 odels of three distinct types of Schiff base rotary motors.

208 l bonds, molecular rotors, and light-powered rotary motors.

209 tion transmission despite the ultrasensitive rotary motors.

210 al propellers that are powered by reversible rotary motors.

211 ion of helical flagellar filaments driven by rotary motors.

212 ers and light-driven and electrically driven rotary motors.

213 It is composed of two rotary motors/generators, FO and F1, which do not slip a

214 h ATP hydrolysis in the cross-bridge driving rotary movement of a lever arm converting torque into li

215 The rotary nanomotor ATP synthase is a central player in the

216 F1-ATPase is the catalytic complex of rotary nanomotor ATP synthases.

217 te reversibility, which forms the basis of a rotary nanomotor driven by temperature.

218 F-type ATP synthases are rotary nanomotor enzymes involved in cellular energy met

219 The development of rotary nanomotors is crucial for advancing nanoelectrome

220 FOF1 ATP synthases are rotary nanomotors that couple proton translocation acros

221 Fast ROtary Nonlinear Spatial ACquisition (FRONSAC) was recen

222 e Ti-bound biofilms for 30 seconds each: (1) rotary nylon brush; (2) Ti brush; (3) water-jet on high

223 a, spastic quadriplegia, dystonic movements, rotary nystagmus, and impaired gaze and hearing.

224 found that the landscape along the relevant rotary path is determined by the electrostatic free ener

225 l microtubules, with domains describing slow rotary patterns.

226 This result shows that rotary photon drag applies to images as well as polariza

227 Because this rotary photon drag has a contribution that is inversely

228 day by making financial contributions to the Rotary PolioPlus program, participating in national immu

229 which the angular velocity is limited by the rotary position at which ATP binding occurs and by the d

230 ratio of the propulsive power output to the rotary power input provided by the motors, is found to b

231 results in anisotropic optical activity and rotary power, which can be experimentally observed as a

232 FT calculations, demonstrate that during the rotary process of the motor, as the rigid substituent be

233 at led to newer motor designs with optimized rotary properties at variable activation wavelengths.

234 cluding twitching motility, effector export, rotary propulsion, nutrient uptake, DNA uptake, and even

235 The V-ATPase is a multisubunit, rotary proton pump whose precise role in homotypic fusio

236 Pleasanton, Calif; n=16) or continuous-flow rotary pump with an axial design operating at a fixed ro

237 Over the past 2 years, a number of smaller rotary pumps have been introduced into clinical trials i

238 nical trials in the United States with three rotary pumps in both bridge-to-transplant and destinatio

239 Pushers are novel descending aorta rotary pumps that directly increase renal artery pressur

240 Continuous-flow rotary pumps with axial design are increasingly used for

241 d sets of residues that collectively undergo rotary rearrangements implicated in ribosome function.

242 In particular, near-rotary-resonance relaxation dispersion (NERRD) experimen

243 persion techniques (Bloch-McConnell and near-rotary-resonance) give complementary information about t

244 psy by using a phase-cycled stimulus-induced rotary saturation (PC-SIRS) approach with spin-lock (SL)

245 s enabled the separation of T2* effects from rotary saturation effects.

246 electrophoresis using a folded channel and a rotary scanner to interrogate the separation at multiple

247 The rotary Scheimpflug camera (Pentacam(R) type) analyzed th

248 Rotary Shadow electron microscopy of purified CsgG sugge

249 olarization interferometry and visualized by rotary shadow electron microscopy.

250 motor domains appear as paired particles by rotary-shadow electron microscopy (EM) and circular dich

251 on shows greater helicity by CD analysis and rotary-shadow EM reveals a stalk joined to one large or

252 linking, analytical ultracentrifugation, and rotary shadowed electron microscopy revealed that CARMIL

253 arrays by directly superimposing replicas of rotary shadowed images of rows of feet, obtained from is

254 further supported by electron microscopy of rotary shadowed molecules.

255 Electron microscopy of rotary shadowed specimens yielded a variety of alphaIIbb

256 d striated muscle tropomyosin molecules were rotary-shadowed and compared by means of electron micros

257 Electron microscopy of rotary-shadowed periplakin demonstrated thin flexible mo

258 th and without tilting, and from deep-etched rotary-shadowed replicas.

259 The persistence lengths along the shaft of rotary-shadowed smooth and striated muscle tropomyosin m

260 Rotary shadowing electron microscopy of molecules of BMP

261 Rotary shadowing electron microscopy of TSP-1 has shown

262 Rotary shadowing electron microscopy revealed zizimin1 t

263 Rotary shadowing electron microscopy, combined with limi

264 Using rotary shadowing followed by electron microscopy, we ide

265 Transmission electron microscopy after rotary shadowing revealed the appearance of rodlike stru

266 of isolated PSDs using immunogold labeling, rotary shadowing, and electron microscopic tomography.

267 P-driven motor (F(1)), connected by a common rotary shaft, and catalyzes proton flow-driven ATP synth

268 on pre-cut Carrara marble cylinders using a rotary shear apparatus at conditions relevant to earthqu

269 In particular, rotary shear experiments conducted at seismic slip rates

270 c and thermodynamic parameters show that the rotary speed is affected by the rigidity of the substitu

271 in barrier height and, as a consequence, the rotary speed.

272 structural analyses have revealed different rotary states for disassembled V(1) and V(o), a mismatch

273 We identify this rotary step as the ATP-dependent substep, and find that

274 iven ATP synthase (FOF1) is comprised of two rotary, stepping motors (FO and F1) coupled by an elasti

275 Constant-velocity rotary stimuli in clockwise and counterclockwise directi

276 chanism of how phosphate release generates a rotary substep as follows.

277 etic and mechanistic description of the main rotary substep in the synthetic cycle of mammalian ATP s

278 -terminal domain of subunit a approaches the rotary subunits in free V(0), suggesting a possible mech

279 e how an imidazolyl ring incorporated into a rotary switch based on a hydrazone enables a switching c

280 ational changes within an embedded hydrazone rotary switch that steers the robotic arm.

281 e of a chemically controlled configurational rotary switch.

282 cal coiled-coil linker; light is acting as a rotary switch.

283 These chemically controlled configurational rotary switches exist primarily as the E isomer at equil

284 system is demonstrated where the exotic dual rotary switching behavior provides a unique and sophisti

285 meter and powders within the feed frame of a rotary tablet press is used to simulate the movement of

286 placements of neighboring molecules near the rotary transition states for 1A and 1B can be as large a

287 tted around the hexamer, reveal a processive rotary translocation mechanism and substrate-responsive

288 l NPG based actuator by utilizing a modified rotary triboelectric nanogenerator (TENG).

289 n of the 2 salt bridge networks via a 3-fold rotary twist induced by substrate binding.

290 Angular rotary twist, the dominant ring motion, was estimated to

291 hnical note, we design and fabricate a novel rotary valve and demonstrate its feasibility for perform

292 V device that is attached to a multiposition rotary valve as a central design unit is demonstrated by

293 A four rotary valve configuration allowed the usage of a single

294 rolled microsyringe pump and a multiposition rotary valve for handling aqueous and organic solutions

295 perature vaporization injector in place of a rotary valve or backflush system to divert solvent, a na

296 A face-seal rotary valve provided a means for switching between samp

297 Hundreds of thousands of Rotary volunteers have provided support for polio eradic

298 We propose a kinematic model of the rotary walking mode based on generic features of penetra

299 quency omega, and a dramatic transition from rotary walking to slow swimming occurs when phi becomes

300 very direction on the c-plane of GaN through rotary wear experiment.