ライフサイエンスコーパス: depolymerize

1 opensity of capsid protein to polymerize and depolymerize.

2 t the mitotic spindle as astral microtubules depolymerize.

3 the tether force that vanish when F-actin is depolymerized.

4 d harsh treatments (e.g., formic acid) to be depolymerized.

5 e time before opening irreversibly and fully depolymerizing.

6 enting newly elongating actin filaments from depolymerizing.

7 ve enzymes and that intact OMVs were able to depolymerize a broad range of linear and branched hemice

8 (CAP) and Cofilin synergize to processively depolymerize actin filament pointed ends at a rate 330-f

9 ereby counteracts MICAL1, an enzyme known to depolymerize actin filaments by direct oxidation.

10 a unique formin that can both polymerize and depolymerize actin filaments.

11 In zebrafish ZF4 cells, Afp18(G) depolymerizes actin stress fibres by mono-O-GlcNAcylatio

12 CDT depolymerizes actin, causes formation of microtubule-bas

13 Depolymerizing actin filaments or decreasing actomyosin

14 al mobility of PSGL-1 similarly increased by depolymerizing actin filaments with latrunculin B or by

15 of ErbB2 compared to ErbB3 was abolished by depolymerizing actin filaments, whereas ErbB2 expression

16 -cadherin-induced cell invasion increase via depolymerizing actin filaments.

17 olished by blocking cell movement (either by depolymerizing actin with latrunculin A or by inhibiting

18 Depolymerizing actin with latrunculin B reduced cross-li

19 pounds 3, 4, and 9 showed potent microtubule depolymerizing activities, while compounds 6-8 had sligh

20 ification inactivates the actin severing and depolymerizing activity of cofilin.

21 The microtubule (MT)-depolymerizing activity of MCAK/Kif2C can be quantified

22 kinase pathway that locally inhibits the MT depolymerizing activity of mitotic centromere-associated

23 Also, the depolymerizing activity of the motor does not contribute

24 As a consequence of their depolymerizing activity, these kinesins increase dynamic

25 transport kinesins also impair MCAK/Kif2C's depolymerizing activity.

26 fferentially control a novel Eg5 microtubule depolymerizing activity.

27 s, as detected by electron microscopy, which depolymerized after zinc chelation.

28 ntly labeled structures are sensitive to the depolymerizing agent latrunculin B (Lat B), demonstratin

29 Further, the F-actin-depolymerizing agent latrunculin induced recall deficit

30 Although the MT depolymerizing agent nocodazole affected dynamic MTs, HI

31 yeast cells are treated with the microtubule-depolymerizing agent nocodazole.

32 Colchicine, a microtubule-depolymerizing agent that is used in prophylaxis and tre

33 3 identify it as a novel, potent microtubule depolymerizing agent with antitumor activity.

34 Treatment of APCs with the actin filament depolymerizing agent, cytochalasin D, as well as knockdo

35 t with colchicine (10 microM), a microtubule-depolymerizing agent, or paclitaxel (10 microM) a microt

36 QCM-D data from cells subjected to an actin depolymerizing agent.

37 Studies showed that microtubule-depolymerizing agents (MDA) not only disassembled microt

38 otoxin is one of the most potent microtubule depolymerizing agents and has served as an important lea

39 microtubule polymers elicited by microtubule depolymerizing agents is blocked by increasing intracell

40 We previously reported that actin-depolymerizing agents promote the alkalization of the Go

41 Diverse microtubule-depolymerizing agents protected mutant huntingtin-expres

42 Under roasting conditions, polysaccharides depolymerize and also are able to polymerize, forming ne

43 oling cycle where the stacks first partially depolymerize and then polymerize again with the still ex

44 Procyanidin oxidation products were depolymerized and the evolution of their markers was mon

45 Second, the microtubules are depolymerized and the granules are released.

46 scence, the nuclear microtubule array slowly depolymerizes and, by pulling attached centromeres back

47 on, our studies provide new insight into how depolymerizing and capping enzymes can lead to MT destab

48 To do so, the kinetochore must hold on to depolymerizing and polymerizing microtubules.

49 Here we identify cofilin1, an actin depolymerizing and severing protein, as a downstream tar

50 tin-binding protein cofilin to stimulate the depolymerizing arm of the cycle, how PAK1 might trigger

51 olymerized within the SR at rest and that it depolymerized as [Ca(2+)] went down: fully when calcium

52 an be rescued by nocodazole treatment, which depolymerizes astral MTs, or by overexpression of CLASP1

53 the capacity of filaments to polymerize and depolymerize at their ends in response to cellular condi

54 Polymers that depolymerize back to monomers can be repeatedly chemical

55 terion exchange with a surfactant, it can be depolymerized back into monomer upon relatively mild the

56 This sc-material can be fully depolymerized back to rac-monomer in a quantitative yiel

57 ird (G3) and second (G2) generation catalyst depolymerize BBs significantly faster than Grubbs' first

58 Crocin depolymerized both the interphase and mitotic microtubul

59 phase onset when microtubules are completely depolymerized but not in the presence of relatively few

60 in filaments and microtubules polymerize and depolymerize by adding and removing subunits at polymer

61 yethylene terephthalate (PET) is selectively depolymerized by a carbon-supported single-site molybden

62 While microtubules in nonneuronal cells are depolymerized by cold, Ca(2+), or antimitotic drugs, neu

63 In this study alginate polymer was depolymerized by heat treatment.

64 l, all MT minus ends that reach the pole are depolymerized by kinesin-13.

65 ng of weakly Bronsted acidic OH-defect sites depolymerizes cellulose under mild conditions, the natur

66 By depolymerizing cellulose, hemicelluloses, and lignin sep

67 In vitro, depolymerized clathrin forms a stable complex with Hsc70

68 g from an inactivating mutation of the actin-depolymerizing cofactor Wdr1.

69 g2-g3 linker in determining the open F-actin depolymerizing-competent shape of G1-G3 in this conditio

70 to CO(2) requires oxidative mechanisms that depolymerize complex molecules into smaller, soluble mon

71 treating Chlamydomonas cells with the actin-depolymerizing compound cytochalasin D resulted in rever

72 tability against cold and nocodazole-induced depolymerizing conditions.

73 CD(r) polymer with the unique capability of depolymerizing continuously and completely in the solid

74 To introduce pits into a cell wall, plants depolymerize cortical microtubules, which prevents subse

75 , severe cell membrane disturbances based on depolymerized cortical actin and an elevated Lyn kinase

76 The objective of this study was to depolymerize cranberry procyanidins, particularly the po

77 The most active catalyst depolymerized crystalline cellulose without prior pretre

78 a kinesin-13 of Drosophila melanogaster that depolymerizes cytoplasmic microtubules.

79 ell as in presence of structurally intact or depolymerized cytoskeletal microtubules.

80 Animals grown with a MT depolymerizing drug caused synthetic defects in neurite

81 This could be mimicked by the actin-depolymerizing drug latrunculin B or by reducing ROCK ac

82 oduction of a brief pulse of the microtubule-depolymerizing drug nocodazole allowed spindle assembly

83 ed tension by treatment with the microtubule-depolymerizing drug nocodazole or compromising kinetocho

84 ore-microtubule interaction by a microtubule depolymerizing drug nocodazole.

85 ratinib acts in synergy with the microtubule-depolymerizing drug vinorelbine to promote apoptosis, su

86 ays that are hypersensitive to a microtubule-depolymerizing drug.

87 could be rescued in cells treated with actin-depolymerizing drugs by mechanically constraining nucleu

88 calization was altered in the presence of MT-depolymerizing drugs, but growth of IAV in all of the ce

89 sult in increased sensitivity to microtubule-depolymerizing drugs, indicative of a mild impact of thi

90 are also inhibited by microtubule- and actin-depolymerizing drugs, invoking both cytoskeletal systems

91 polymer that can rapidly and quantitatively depolymerize due to its low ceiling temperature.

92 TTL (TTL-E331Q) to separate the microtubule depolymerizing effects of TTL from its enzymatic activit

93 escue: 1) an "end-driven" model in which the depolymerizing end stochastically switches to a stable s

94 regation, outer kinetochore components track depolymerizing ends of microtubules to facilitate the se

95 these sites is influenced by changes in the depolymerizing ends.

96 have been characterized, studies of alginate-depolymerizing enzymes have lagged.

97 osting the activity of well-known hydrolytic depolymerizing enzymes.

98 spine and reorganizing it to be resistant to depolymerizing events.

99 Because of its ability to rapidly depolymerize F-actin, plasma gelsolin has emerged as a t

100 We then depolymerized F-actin to decouple vesicle diffusion from

101 Members of the actin-depolymerizing factor (ADF) and cofilin protein family p

102 In higher eukaryotes, the related actin depolymerizing factor (ADF) and cofilin proteins are ess

103 Inactivation of actin depolymerizing factor (ADF) causes sustained actin polym

104 Cofilin/actin-depolymerizing factor (ADF) proteins are critical nodes

105 actin interacting protein1 (AIP1) and actin depolymerizing factor (ADF).

106 in (Dstn) gene, which is also known as actin depolymerizing factor (ADF).

107 we found that NGF treatment increases actin-depolymerizing factor (ADF)/cofilin activity and growth

108 Disassembly of actin filaments by actin-depolymerizing factor (ADF)/cofilin and actin-interactin

109 Here, we test the hypothesis that actin depolymerizing factor (ADF)/cofilin contributes to stoch

110 Actin depolymerizing factor (ADF)/cofilin controls actin turno

111 Actin depolymerizing proteins of the actin depolymerizing factor (ADF)/cofilin family are essential

112 Proteins of the actin depolymerizing factor (ADF)/cofilin family are the centr

113 Proteins of the actin-depolymerizing factor (ADF)/cofilin family have been sho

114 ring synaptic plasticity, in which the actin depolymerizing factor (ADF)/cofilin family of actin-asso

115 Cofilin is a member of the actin depolymerizing factor (ADF)/cofilin family of proteins.

116 ration factor (GMF) is a member of the actin-depolymerizing factor (ADF)/cofilin family.

117 to ATP and recycle actin monomers from actin-depolymerizing factor (ADF)/cofilin for new rounds of fi

118 We report that depletion of actin depolymerizing factor (ADF)/cofilin proteins in human ce

119 ks requires actin filament severing by actin-depolymerizing factor (ADF)/Cofilin proteins.

120 ar junctions as a model, we found that actin depolymerizing factor (ADF)/cofilin regulated actin-depe

121 Aip1p cooperates with actin-depolymerizing factor (ADF)/cofilin to disassemble actin

122 Actin depolymerizing factor (ADF)/cofilins are essential regul

123 the single allele of Toxoplasma gondii actin depolymerizing factor (TgADF) has strong actin monomer-s

124 repeat domain 1 (WDR1), an enhancer of actin-depolymerizing factor activity, is downregulated in plat

125 We identified the actin depolymerizing factor ADF/cofilin1, which mediates high

126 roteins Cyclase-Associated Protein and Actin-Depolymerizing Factor are identified as key downstream t

127 d with robust dephosphorylation of the actin depolymerizing factor cofilin by PP1 and PP2A serine/thr

128 ol of RhoA and of cortactin toward the actin-depolymerizing factor cofilin.

129 LIM kinase and phosphorylation of the actin-depolymerizing factor cofilin.

130 hat phosphorylates and inactivates the actin-depolymerizing factor cofilin.

131 east two-hybrid analysis uncovered the actin-depolymerizing factor gelsolin, the membrane glycoprotei

132 ner that interacts with the N-terminal actin depolymerizing factor homology domain (ADFH) domain of m

133 Deactivation of cofilin, an actin depolymerizing factor is required for spinogenesis.

134 ry cilium, where CEP170 recruits microtubule-depolymerizing factor KIF2A to disassemble cilium.

135 llen allergens, polygalacturonase, and actin depolymerizing factor were characterized for the first t

136 proteins identified was cofilin-1, an actin depolymerizing factor which regulates neuronal dendrite

137 he actin-binding proteins profilin and actin-depolymerizing factor, because they are essential and th

138 Cofilin, the major actin depolymerizing factor, modulates actin dynamics that con

139 y downstream target of PAK and a major actin depolymerizing factor, prevented Shank3 siRNA from reduc

140 of the Rho target protein cofilin, an actin-depolymerizing factor.

141 d by the inhibitor of cofilin, a major actin-depolymerizing factor.

142 indicating that AtADF4 is a bona fide actin-depolymerizing factor.

143 through phosphorylation of cofilin, an actin-depolymerizing factor.

144 AMP-induced alterations phenocopied an ACTIN DEPOLYMERIZING FACTOR4 (ADF4) knockout mutant.

145 Actin-depolymerizing factors (ADFs) are a group of actin-bindi

146 the activity of a conserved family of actin-depolymerizing factors (ADFs), whose primarily function

147 binds monomeric actin with a K(d) of 9.0 nM, depolymerizes filamentous actin in vitro and in A549 (no

148 Latrunculin B, which depolymerizes filamentous actin, markedly slows growth b

149 When HS/heparin is enzymatically depolymerized for compositional analysis, 3-O-sulfated g

150 for creating aromatic poly(carbamates) that depolymerize from head-to-tail in low dielectric constan

151 c filaments that are rapidly polymerized and depolymerized from a pool of pilin subunits.

152 s-ends of KMTs have selectively detached and depolymerized from the centrosome.

153 These enzymes depolymerize fucoidan into fucose, which is metabolized

154 In agreement with a role for the actin-depolymerizing function of ADF3 in defense against the G

155 g that Nm23-H1 binding inactivated the actin-depolymerizing function of Gelsolin to inhibit cell moti

156 Bacterial polysaccharide lyases depolymerize GAGs in beta-elimination reactions, and the

157 commonly used actin-disrupting drugs do not depolymerize giActin structures.

158 Ca-gamma-actin depolymerizes half as fast as does beta-actin.

159 onsortia or single organisms are required to depolymerize highly complex glycans.

160 otubules in cells below 20 degrees C rapidly depolymerize in a temperature-dependent manner whereas t

161 les colliding with cell boundaries zip-up or depolymerize in an angle-dependent manner, as predicted

162 h the cytosol of HeLa cells within 5 min and depolymerize in less than 1 min to release the native su

163 planta, and the mechanisms by which they are depolymerized in microbial ecosystems.

164 When microtubules are depolymerized in spreading cells, they experience morpho

165 onstrate the strategy and now are capable of depolymerizing in the context of rigid, solid-state poly

166 on, we do not understand how actin filaments depolymerize inside cells.

167 ese data show that vimentin filaments do not depolymerize into individual subunits; they recompose by

168 polymers (BBCPs) are shown to quantitatively depolymerize into linear diblock polymer grafts.

169 from simple monomers and can be designed to depolymerize into nontoxic products.

170 After s-SWNT separation, the polymer can be depolymerized into monomers and be cleanly removed under

171 acteria cultivated in the vessel, the PGA is depolymerized into oligogalacturonates (UGA), which are

172 emical route 1, alkali lignin was chemically depolymerized into vanillin and syringate as major produ

173 We show that expression of the microtubule depolymerizing kinesin KIF2C is induced by transformatio

174 liary cap is critical to recruit the tubulin-depolymerizing kinesin Klp59D, required for regulation o

175 A CLASP family MT stabilizer and the depolymerizing kinesin MCAK are differentially required

176 Here we identify Klp10A, a microtubule-depolymerizing kinesin of the kinesin-13 family, as the

177 We show that Kif24, a microtubule depolymerizing kinesin, is phosphorylated by Nek2, which

178 MTs is restricted in the steady state by the depolymerizing kinesin-13 family member KLP-7.

179 e-associated kinesin (MCAK) is a microtubule-depolymerizing kinesin-13 member that can track with pol

180 multinucleation by targeting the microtubule depolymerizing kinesins and inhibiting AR.

181 sms for microtubule length control, based on depolymerizing kinesins and severing proteins, have been

182 high-affinity binding state for microtubule-depolymerizing kinesins is in a closed conformation.

183 ee tubulin, which contrasts with microtubule-depolymerizing kinesins that preferentially bind free tu

184 tivity is not universal and that microtubule-depolymerizing kinesins utilize a distinct conformationa

185 member of an important class of microtubule-depolymerizing kinesins, KLP10A, is required for the pro

186 ata support a model in which KLP59D directly depolymerizes kinetochore-associated plus ends during an

187 n simplified peroxide digestion that rapidly depolymerizes large polysaccharide chains to small oligo

188 ient conditions, the poly(CO2) spontaneously depolymerizes, leading to a sorbent that can be easily r

189 ow-through reactors as an analytical tool to depolymerize lignin in poplar with naturally varying S/G

190 degrading peroxidase from Rodococcus jostii, depolymerizes lignin and reduces recalcitrance in transg

191 d species, Ceriporiopsis subvermispora, also depolymerizes lignin but may do so with relatively littl

192 d neurotrophic factor shows that the F-actin depolymerizing macrolide toxin mycalolide B (MB) rapidly

193 The Kif18A motor domain also depolymerizes microtubule plus and minus ends.

194 physically interact with polymerizing versus depolymerizing microtubule bundles, and whether they use

195 omplex binds to microtubules and tracks with depolymerizing microtubule ends [2].

196 netochore-localized Ska1 complex tracks with depolymerizing microtubule ends and associates with both

197 etween intersecting microtubules, and tracks depolymerizing microtubule ends.

198 omplexes to bind microtubules, especially to depolymerizing microtubule plus ends, but how this is ac

199 s, the Ndc80 complex couples the energy in a depolymerizing microtubule to perform the work of moving

200 e kinesin superfamily of motor proteins that depolymerize microtubules (MTs) and have no motile activ

201 Motor proteins from the kinesin-8 family depolymerize microtubules by interacting with their ends

202 Kif24 is able to bind and depolymerize microtubules in vitro.

203 ses: the kinesin-13 proteins, which directly depolymerize microtubules, and the kinesin-8 proteins, w

204 inesin family members (KIFs) KIF2A and KIF2C depolymerize microtubules, unlike the majority of other

205 ability revealed that both TTL and TTL-E331Q depolymerize microtubules, while VASH1 and SVBP depletio

206 o resistant to calcium as well as drugs that depolymerize microtubules.

207 g-pool model that incorporates proteins that depolymerize microtubules.

208 D5 depolymerized microtubules in cultured cells and produce

209 It depolymerized microtubules, induced spindle defects, and

210 in MCF-7 cells and delayed the reassembly of depolymerized microtubules.

211 In contrast, Kar3Cik1 depolymerizes microtubules during mating but cross-links

212 p60 katanin, an AAA protein that severs and depolymerizes microtubules, is subject to multiple modes

213 However, it is still unclear how kinesin-8 depolymerizes microtubules.

214 etochore-associated Ska1 complex hangs on to depolymerizing microtubules and brings some important fr

215 Depolymerizing microtubules did not affect the ability o

216 le at the interface with polymerizing versus depolymerizing microtubules remains unclear.

217 Surprisingly, we discovered that depolymerizing microtubules stiffens embryonic tissues b

218 e the ring-shaped Dam1 complex to slide down depolymerizing microtubules to move chromosomes, but cur

219 xpansion, and the asymmetry was removed upon depolymerizing microtubules with oryzalin.

220 dothelial cell adhesion molecule 1 antibody, depolymerizing microtubules, or microinjection of an ant

221 ka1 and Ndc80 complexes that associates with depolymerizing microtubules, potentially by interacting

222 metaphase, one sister kinetochore couples to depolymerizing microtubules, pulling its sister along po

223 olecular kinetochore must remain attached to depolymerizing microtubules, which drive chromosome move

224 How kinetochores associate with depolymerizing microtubules, which undergo dramatic stru

225 compromise the kinetochore's ability to grip depolymerizing microtubules.

226 ely probe Hec1's role on polymerizing versus depolymerizing microtubules.

227 nstead, they processively tracked shrinking, depolymerizing minus ends.

228 -stabilized microtubules and the microtubule-depolymerizing mitotic centromere-associated kinesin (MC

229 Instead, the microtubule depolymerizing motor protein kif2a functions to modulate

230 esins instead uniquely recognize MT ends and depolymerize MT protofilaments.

231 ion of Kip3 facilitates its association with depolymerizing MT plus ends, where Kip3 promotes rescue

232 in dimers from the ends of MTs, appearing to depolymerize MTs.

233 Surprisingly, all cells with depolymerized MTs rapidly repolymerize their MTs after a

234 It has been shown that depolymerizing MTs with nocodazole abrogates the stathmi

235 g fewer filaments into a smaller volume, the depolymerizing network shrinks and thereby generates suf

236 n-tropomyosin filaments to protect them from depolymerizing, not elongating.

237 able of responding to a different signal and depolymerizing once the signal reacts with the trigger.

238 When cells are treated with drugs that depolymerize or stabilize the cytoskeleton or the nucleu

239 s when ParB complexes have a passive role in depolymerizing ParA filaments.

240 ghout their ~40-s lifetime unless the mother depolymerized past the branch point.

241 Specifically, the I. sakaiensis PETase depolymerizes PET, liberating soluble products, includin

242 addition, SALS-WH2 can bind to but fails to depolymerize phalloidin- or jasplakinolide-bound actin f

243 rylation of beta-catenin and two microtubule depolymerizing phosphorylations of Tau, potentially expl

244 bules or forming end-on attachments to their depolymerizing plus-ends.

245 d means for efficient and safe production of depolymerized-polymer derivatives.

246 rbohydrate-active enzymes that synthesize or depolymerize polysaccharides by chain translocation mech

247 To depolymerize polysaccharides to soluble sugars, many org

248 ons with experiments suggests that kinesin 8 depolymerizes processively, i.e., one motor can remove m

249 Knowing that the F-actin depolymerizing property of gelsolin resides in its N ter

250 2(LRR1) leads to the activation of the actin-depolymerizing protein cofilin, dramatic reorganization

251 ity by controlling the activity of the actin depolymerizing protein Cofilin.

252 ardium were enriched for cofilin-2, an actin-depolymerizing protein known to participate in neurodege

253 , by way of a direct sequestration of the MT depolymerizing protein Stathmin 1 (STMN1), and we provid

254 sis identified Stathmin-1 (STMN1), a tubulin-depolymerizing protein, as a potential disease modifier

255 d thereby inactivation of Cofilin1, an actin-depolymerizing protein, in ATG7-depleted cells.

256 can arise from a concentration gradient of a depolymerizing protein, such as kinesin-13 in Giardia, a

257 Stabilizing and depolymerizing proteins control the steady-state levels

258 Actin depolymerizing proteins of the actin depolymerizing fact

259 red: a linear and an exponential gradient of depolymerizing proteins.

260 enhanced dynamics upon treatment with actin depolymerizing reagents in elongated and polarized geome

261 affinity for Rev and was able to effectively depolymerize Rev filaments, as shown by both surface pla

262 an lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts la

263 Depolymerized right after use, the best siCPDs are nonto

264 nate, provides a poly(ethyl glyoxylate) that depolymerizes selectively upon irradiation with UV light

265 ng over minutes activates the actin filament depolymerizing/severing factor cofilin, alters F-actin d

266 ion of C for O is also attained in PDCs with depolymerized silica-rich domains containing lithium, as

267 While viscosity of depolymerized silicate melts increases with pressure con

268 a few seconds, yet in vitro actin filaments depolymerize slowly over minutes.

269 f both AurA and AurB results in a failure to depolymerize spindle microtubules (MTs) in anaphase afte

270 In dividing cells, depolymerizing spindle microtubules move chromosomes by

271 oposed to facilitate kinetochore movement on depolymerizing spindle microtubules.

272 ed tubulin protofilaments, and that stathmin depolymerizes stabilized protofilament-rich polymers.

273 Microtubules polymerize and depolymerize stochastically, a behavior essential for ce

274 of 51:5:19:25 or 59:5:11:25 could completely depolymerize tamarind XG to free Glc or Xyl, respectivel

275 ess than 100 ACD molecules are sufficient to depolymerize the actin filaments of a fibroblast cell in

276 ngolipid domains are disrupted by drugs that depolymerize the cells actin cytoskeleton, cholesterol m

277 urface saponification is effective enough to depolymerize the cutin into its monomeric constituents t

278 Using latrunculin A to depolymerize the cytoskeleton during endocrine induction

279 ssess a diverse array of secreted enzymes to depolymerize the main structural polysaccharide componen

280 ls with high concentrations of nocodazole to depolymerize the microtubule network.

281 terium Bacteroides thetaiotaomicron (Bt) can depolymerize the most structurally complex glycan, the p

282 e one composed of the first 28-161 residues, depolymerized the F-actin much faster than the native ge

283 The apparatus that depolymerizes the backbone of rhamnogalacturonan-I is pa

284 d genes during growth on wheat arabinoxylan, depolymerizes the polysaccharide into its component suga

285 Depolymerizing the actin cytoskeleton during cytokinesis

286 When actin was depolymerized, the glycoprotein concentrations dispersed

287 derstanding the mechanisms by which microbes depolymerize their target substrates.

288 The cellular mechanisms enabling actin to depolymerize this fast have so far remained obscure.

289 nes utilized by the colonic Bacteroidetes to depolymerize this polysaccharide.

290 itro, calsequestrin must polymerize and then depolymerize to release it.

291 large oligosaccharides that are subsequently depolymerized to mannose by the action of periplasmic en

292 t concentrations of cytochalasin D, an actin-depolymerizing toxin.

293 their poly(ethyl glyoxylate) blocks rapidly depolymerize upon UV irradiation.

294 ls, Glk1 polymerized upon sugar addition and depolymerized upon sugar withdrawal.

295 The extract was depolymerized, using 0.1 or 1M methanolic HCl, with (+)-

296 Furthermore, when microtubules are depolymerized with colchicine just before metaphase the

297 nidulans, we find that MTs are regulated to depolymerize within forming fungal biofilms.

298 ereas regions near new microtubule plus ends depolymerized without any observable change in shape.

299 hese two enzymes function synergistically to depolymerize xylan.

300 AxlA together with beta-glucosidase depolymerized xyloglucan heptasaccharide.