ライフサイエンスコーパス: nanodomain

1 ormed between cells, which create signaling 'nanodomains'.

2 0.81 ( 220 mAh g(-1)) were identified in the nanodomain.

3 channels, enabling near-field imaging of the nanodomain.

4 ain out-of-phase oscillations outside of the nanodomain.

5 m regulating the dynamic and organization of nanodomains.

6 CD22 to be highly mobile and organized into nanodomains.

7 AMPAR nanodomains segregated away from NMDAR nanodomains.

8 taxin-1A in and out of partially overlapping nanodomains.

9 as LRRTM2 is organized in compact and stable nanodomains.

10 maR2 is confined by sphingolipid/cholesterol nanodomains.

11 morphous Si (a-Si) band, embedded with dh-Si nanodomains.

12 he results were interpreted in terms of RTIL nanodomains.

13 l with alternately segregated donor/acceptor nanodomains.

14 DGs and the formation of perigranular Ca(2+) nanodomains.

15 zation rotation is an abundance of sub-50 nm nanodomains.

16 the charge distribution in the local charged nanodomains.

17 ion of the size of these highly concentrated nanodomains.

18 ses underpinning synthetic control of defect nanodomains.

19 ese findings for theoretical descriptions of nanodomains.

20 in small ( approximately 80 nm in diameter) nanodomains.

21 anometers for highly ordered, single-polymer nanodomains.

22 bility, consistent with their confinement in nanodomains.

23 and mutant integrin partitioning into lipid nanodomains.

24 eceptors was interrupted by dwellings within nanodomains.

25 etween nucleosome clutches, RNAP II, and RNA nanodomains.

26 g the role of oncogenic APC in reshaping Wnt nanodomains.

27 of the NPC1-dependent construction of lipid nanodomains.

28 inctly regulated by clathrin and tetraspanin nanodomains.

29 ins are organized and functional in membrane nanodomains.

30 izes to planar boundaries of transient polar nanodomains.

31 h energy densities designed with polymorphic nanodomains.

32 s to rotate continuously between the a and c nanodomains.

33 the formation and functionality of membrane nanodomains.

34 from the dynamic evolution of ferroelectric nanodomains.

35 exclusively in thin interdigitating membrane nanodomains.

36 t motion states, two of them associated with nanodomains.

37 ersistently displayed higher mobility within nanodomains.

38 ric fields and depletion of local sodium ion nanodomains.

39 IgG and poly(N-isopropylacrylamide) (PNIPAM) nanodomains.

40 the fragmentation of gephyrin in subsynaptic nanodomains.

41 ated with the promoted formation of gephyrin nanodomains.

42 ed signalling components within dedicated PM nanodomains.

43 daries between randomly oriented crystalline nanodomains.

44 ent visits (~100 ms) of presynaptic VGCCs in nanodomains (~80 nm) that were controlled by neuronal ne

45 ten relies on Ca(2+) computations within the nanodomain-a conceptual region extending tens of nanomet

46 ctor X, which binds directly to the membrane nanodomain adjacent to tissue factor.

47 Normally distributed in linear quadrilateral nanodomains along the flagellum, the complex lacking Cat

48 ssembly of the linear arrangement of CatSper nanodomains along the sperm tail and regulates the pH an

49 l complexes organize linear Ca(2+) signaling nanodomains along the sperm tail.

50 ynaptic densities, we observed GluA2-lacking nanodomains alongside regions with robust GluA2 expressi

51 emonstrate that detergent-resistant membrane nanodomains, also known as lipid rafts, are the primary

52 d that different CTLs rarely occupy the same nanodomain, although they appear colocalized using wide-

53 that consists of the ordered pseudographitic nanodomains among disordered highly nitrogen-doped segme

54 a1 (PI4Kalpha1) to the plasma membrane via a nanodomain-anchored scaffolding complex.

55 AMPARs are stabilized reversibly in these nanodomains and diffuse freely outside them.

56 SMOLM images resolve nanodomains and enzyme-induced compositional heterogenei

57 edict that both the Turing pattern-generated nanodomains and experimentally measured nanodomains demo

58 alectins restored lateral diffusion in lipid nanodomains and JAK/STAT signaling in patient cells, whe

59 c receptor interactions with actin and lipid nanodomains and reveal a new function for receptor glyco

60 s by dynamically disrupting Na(V)1.5-rich ID nanodomains and slowing atrial conduction.

61 l arrhythmia susceptibility by disrupting ID nanodomains and slowing atrial conduction.

62 diffraction techniques used to detect defect nanodomains and the subnanometer imaging used to observe

63 eraction leading to the formation of adhesin nanodomains and trans-interaction between amyloid sequen

64 luence of the A-site cation on local dynamic nanodomains, and consequently, on the macroscopic proper

65 c field coupling, intercellular cleft sodium nanodomains, and LQT3-associated mutant channels, myocyt

66 h mobility with transient incorporation into nanodomains, and the other pool forms immobile clusters,

67 -order GLP1R organization including membrane nanodomains, and track single receptor subpopulations.

68 Previously, a number of Ca(2+) nanodomains approximations have been developed, for inst

69 These pre- and postsynaptic nanodomains are characterized by a high density of molec

70 Nanodomains are dynamic in their shape and position with

71 rostatic and steric interactions within such nanodomains are known to shape diffusion-limited reactio

72 AMPAR nanodomains are often, but not systematically, colocaliz

73 lly robust insulating and rubbery conducting nanodomains are promising solid-state electrolytes for L

74 DC-SIGN and CD206 nanodomains are randomly distributed on the plasma membr

75 Some of these nanodomains are so small (radius <5 nm) that they cannot

76 The nanodomains are speculated to be of a micellar structure

77 Ca(2+) nanodomains arising from store-operated Orai1 Ca(2+) cha

78 Although stabilization of ordered lipid nanodomains around antigen-crosslinked IgE-FcepsilonRI i

79 ycin, suggesting that critical, local Ca(2+) nanodomains around TPCs stimulate granule exocytosis.

80 rolled whether SK channels were expressed in nanodomains as single entities or as a group of multiple

81 ter resonance energy transfer, which detects nanodomains as well as large domains.

82 localized with synaptic proteins in specific nanodomains, as determined by super-resolution microscop

83 ur results uncover a striking feature of CaV nanodomains, as diffusion-restricted environments that a

84 found these proteins to localize in membrane nanodomains, as observed by colocalization with the nano

85 s rather than liquid-ordered phase-separated nanodomains, as previously thought, with "like/unlike" b

86 We review the main properties of these nanodomains, as well as the methods developed to extract

87 sis to identify previously unrecognized cAMP nanodomains associated with beta-adrenergic stimulation.

88 w that Gpsm2 defines an approximately 200 nm nanodomain at the tips of stereocilia and this localizat

89 exponentially with the area fraction of the nanodomains at fixed surface pressure over the 0.1- to 1

90 lustering at AZs, which likely alters Ca(2+) nanodomains at release sites and thereby affects release

91 Our results do not support the presence of nanodomains based on lipid-phase separation in the basal

92 ive in activating gene expression via Ca(2+) nanodomains because it participates in a membrane-delimi

93 We propose that Ca(2+)-signaling nanodomains between lysosomes and sarcoplasmic reticulum

94 We here localized multiple CaMs to the Ca(V) nanodomain by tethering either WT or mutant CaM that lac

95 ransforms to amorphous carbon with graphitic nanodomains by catalytic effect of Fe.

96 ly encoded superhydrophilic-superhydrophobic nanodomains by partially embedding polyvinylidene fluori

97 observed an unexpected and dramatic boost in nanodomain Ca(2+) amplitude, ten-fold higher than predic

98 is provides an accurate approximation to the nanodomain Ca(2+) and buffer concentrations.

99 proved useful in revealing the dependence of nanodomain Ca(2+) distribution on crucial parameters suc

100 However, direct visualization of nanodomain Ca(2+) far exceeds optical resolution of spat

101 ge-sensitive calcium channels, presumably by nanodomain Ca(2+) near the channels, in response to glut

102 strate a key role of the JPH4 and junctional nanodomain Ca(2+) signalling in the pain-like response i

103 Theory predicts that nanodomain Ca(2+) signals differ vastly from the slow su

104 ed in their voltage-dependent gating and use nanodomain Ca(2+) to drive local CaMKII aggregation and

105 ts suggest a model for fast release in which nanodomain Ca(2+) triggers exocytosis of docked vesicles

106 n frog oocytes requires highly localized, or nanodomain, calcium signaling.

107 anized in a random fashion; evidently, these nanodomains can be clustered into larger microdomains th

108 with Ca2+-cAMP dynamics on and away from the nanodomains can be explained by an incoherent feedforwar

109 Crucial questions are whether lipid nanodomains can exist in stable equilibrium in membranes

110 , facilitating the nucleation of polymorphic nanodomains characterized by a slush-like polar structur

111 Within these 'nanodomains', charged nucleotides interact with densely-

112 stributed on the plasma membrane, whereas HA nanodomains cluster on length scales up to several micro

113 We show that in mouse MIN6 beta cells, nanodomain clustering of Ca(2+)-sensitive adenylyl cycla

114 Second, histone nanodomain clusters decompact into mononucleosome fibers

115 r a phase boundary wherein c/a and a(1)/a(2) nanodomains coexist.

116 yer best described as highly strained VO2(B) nanodomains combined with an extra (Ti,V)O2 layer on the

117 a differing localization to plasma membrane nanodomains compared with wild-type alpha(q).

118 ing the existence of a previously unknown SR nanodomain composed of both RyR2 and PLN/sarco/endoplasm

119 atching the short-range Taylor series of the nanodomain concentration with the long-range asymptotic

120 The nanodomains consist of 6:1 DPPC:cholesterol "complexes"

121 In the outer leaflet, distinct nanodomains consisting of gangliosides are observed.

122 imate, as a lower limit, that DC-SIGN and HA nanodomains contain on average two tetramers or two trim

123 These data implicate subsynaptic nanodomains containing a major psychiatric risk molecule

124 ation spectroscopy we demonstrate that these nanodomains containing hundreds of lipid molecules are f

125 Double-nanodomain coupling between somatic plasma membrane and

126 Nanodomain coupling has several functional advantages, i

127 (PV)-expressing interneurons is triggered by nanodomain coupling of P/Q-type Ca(2+) channels, whereas

128 ease is triggered by microdomain rather than nanodomain coupling.

129 Stable ferroelectric nanodomains created in SrTiO3 were observed at temperatu

130 ated nanodomains and experimentally measured nanodomains demonstrate the existence of in-phase and in

131 statistical model indicated that the coronal nanodomains detected likely result from a segmented, gra

132 terol segregates into 10- to 100-nm-diameter nanodomains dispersed throughout primarily dipalmitoylph

133 atio, compartment size, and distance between nanodomains do not affect the existence of in-phase or i

134 P oscillation while the distance between two nanodomains does not.

135 e coexistence of rhombohedral and tetragonal nanodomains embedded in a cubic matrix.

136 tes consist of homogeneously dispersed LixSi nanodomains embedded in a highly crystalline Li2O matrix

137 k of Sph and second, coalescence of existing nanodomains ending in large-scale phase separation.

138 vidual dendritic spines can contain separate nanodomains enriched for either PSD-95 or its closest ho

139 omyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in living cells and in model membranes

140 nm nanoclusters or approximately 300-600 nm nanodomains for potential interaction with IL-22R.

141 s, we predict that intercellular cleft Na(+) nanodomain formation and collapse critically regulates c

142 models of the Ca2+/cAMP pathway and AKAP/AC nanodomain formation that give rise to the two important

143 ains as small as 50 nm in radius and observe nanodomain formation, destruction, and dynamic coalescen

144 partially reversible LiMn(2) O(4) -like sub-nanodomain formation/dissolution process during each cha

145 phosphatidylserine membrane localization and nanodomains formation, which, in turn, tunes ROP6 signal

146 Deficiency of C2CD6 depletes the CatSper nanodomains from the flagellum and results in male steri

147 uate these sequentially-coupled reactions in nanodomain geometries representative of extracellular sy

148 Although the general presence of membrane nanodomains has become widely accepted as fact, fundamen

149 Interestingly, similar disruption of ID nanodomains has been identified in atrial samples from A

150 plexes within the context of plasma membrane nanodomains has remained a highly challenging task.

151 ility in euchromatin, spatial arrangement of nanodomains, histone acetylation, and methylation.

152 Ca(V)3 functionally localized to produce nanodomain hotspots of calcium influx that coupled to ry

153 The investigation of potential nanodomains, however, requires the use of superresolutio

154 observed sensitive variations in the thermal nanodomain IMT behaviour, this suggests that the IMT is

155 UCC1 forms a central CS nanodomain in comparison with other CS-located proteins

156 en Ca(2+) influx and exocytosis changes from nanodomain in low-frequency tuned hair cells ( approxima

157 recruitment of Ca(2+)-sensitive enzymes to a nanodomain in the immediate vicinity of the LTCC by an u

158 +) source describing a single-channel Ca(2+) nanodomain in the presence of a single mobile Ca(2+) buf

159 bservation of ferroelectric and ferroelastic nanodomains in (110)-oriented BiFeO3 (BFO) thin films ep

160 relocalizes into symbiosis-specific membrane nanodomains in a stimulus-dependent manner.

161 Compiling a dynamic map of cAMP nanodomains in defined cell types would establish a blue

162 tion microscopy identified reduced Ankyrin-G nanodomains in dendritic spines.

163 opensity of DAT-AAA to localize to irregular nanodomains in dopaminergic terminals.

164 he existence of ANO1-containing multichannel nanodomains in DRG neurons and suggest that coupling bet

165 , function, and regulation of cAMP-signaling nanodomains in health and disease is essential and will

166 lung surfactant, and can explain the role of nanodomains in its surface activity and inhibition by an

167 tion of room-temperature skyrmion-like polar nanodomains in lead titanate/strontium titanate bilayers

168 ns (MC-FRET) identifies directly 10 nm large nanodomains in liquid-disordered model membranes compose

169 The presence and effect of RTIL nanodomains in molecular solvent/RTIL mixture were inves

170 de strong direct evidence of the presence of nanodomains in molecular solvent/RTIL mixtures.

171 tatistically quantified from over 20 million nanodomains in polycrystalline particles.

172 cent dyes or sQDs were diffusing in confined nanodomains in PSDs, which were stable for 15 min or lon

173 finement of VDCC within sarcolemmal membrane nanodomains in response to varying tonus of C. elegans b

174 Hybrid lipids generate nanodomains in some model membranes and are also abundan

175 shes the physiological relevance of membrane nanodomains in the control of transmembrane receptor sig

176 alated disk, facilitating formation of Na(+) nanodomains in the intercellular cleft between cells.

177 We directly image defect nanodomains in the MOF UiO-66(Hf) over an area of ca. 10

178 to extend the Pade method to estimate Ca(2+) nanodomains in the presence of cooperative Ca(2+) buffer

179 rated iron-rich, redox-active and preceramic nanodomains in the solid state with applications in nano

180 orted here for direct, probe-free imaging of nanodomains in unperturbed membranes open new avenues fo

181 gs suggest that AMPARs rapidly enter stable 'nanodomains' in PSDs with lifetime >15 min, and do not a

182 +) source describing a single-channel Ca(2+) nanodomain, in the presence of a single mobile buffer wi

183 ease in lambda expected from the line-active nanodomains, in analogy to 3D emulsions.

184 is abolished in the GPMVs, whereas transient nanodomain incorporation of ganglioside lipid GM1 is app

185 lar assemblies that exclude cholesterol-rich nanodomains, increase membrane fluidity, and disrupt raf

186 eticulum (ER) membrane, plasma membrane, and nanodomains induced by cholera toxin B.

187 Nanodomains inserted within a crystalline matrix can pro

188 ation that AMPARs are highly concentrated in nanodomains, instead of diffusively distributed in the P

189 irregularly shaped 100-200 nm poly(alanine) nanodomains interspersed within the PEG phase.

190 ated positive feedback that reinforces these nanodomains into polarized domains.

191 ge-carrier trapping times in sp(2) and sp(3) nanodomains is determined.

192 erall view of the cellular landscape of cAMP nanodomains is missing.

193 red environment of cholesterol-rich membrane nanodomains is thought to exclude many transmembrane (TM

194 The key to characterizing nanodomains is to monitor the coincidental secondary ion

195 , the key orchestrator of glutamate receptor nanodomains juxtaposed to the presynaptic glutamate rele

196 tage-activated Cav3.2 Ca(2+) channels at the nanodomain level to support a previously undescribed tra

197 These associations within membrane nanodomains likely maximise interactions between pigment

198 They are involved in the formation of nanodomains ("lipid rafts"), which serve as important si

199 3/CPK21 with ABI1, however, prevented proper nanodomain localization of the SLAH3/CPK21 protein compl

200 ity interfacial connections, and hydrophobic nanodomains maintain bulk integrity via entropic water e

201 heir interplay with proteins, and aspects of nanodomain maintenance and persistence remain poorly und

202 visualising FLS2 and BRI1 within distinct PM nanodomains marked by specific remorin proteins and diff

203 ains, as observed by colocalization with the nanodomain marker remorin Arabidopsis thaliana remorin 1

204 REMs are the best-characterized nanodomain markers via an uncharacterized moiety called

205 +) tuning by the physical composition of the nanodomain may represent an energy-efficient means of lo

206 eir size, fluidity, order and lifetime these nanodomains may represent a relevant model system for ce

207 cell types, NFAT can be activated by Ca(2+) nanodomains near open store-operated Orai1 and voltage-g

208 cepted model of SiCO which is conceived as a nanodomain network of graphene.

209 In the case study on the PbS-Ag system, Ag nanodomains not only contribute to block phonon propagat

210 that the ER-mitochondrial interface hosts a nanodomain of H2O2, which is induced by cytoplasmic [Ca(

211 ured substrates, such printed patterns yield nanodomains of block-copolymers with well-defined sizes,

212 ocal control of BKCa channels by fluctuating nanodomains of Ca(2+).

213 of the grana thylakoid membrane that reveals nanodomains of colocalized PSII and cytb6f complexes.

214 The thin films have nanodomains of crystallinity with lattice spacing simila

215 le-molecule immunolabeling showed that dense nanodomains of PSD-95 were preferentially enriched in AM

216 Vitrification of aqueous nanodroplets yields nanodomains of pure low-density amorphous ice in coexist

217 of these 10(6)-10(7) measurements arise from nanodomains of similar composition, data can be grouped

218 Structured nanodomains of the metallic VO2 locally and reversibly t

219 Caveolae are spherically shaped nanodomains of the plasma membrane, generated by coopera

220 ts gross spatial arrangement within specific nanodomains of these nanoparticles and reveal how compar

221 encapsulate beta-barrel proteins into lipid nanodomains of variable size.

222 nstitutive organization of the proteins in a nanodomain on the apical membrane, which translates loca

223 cally segregates into iodide-rich perovskite nanodomains on a length scale of up to a few hundred nan

224 ed RNAs (glycoRNAs) form precisely organized nanodomains on cancer cell surfaces.

225 pendent neuroexocytosis and are organized in nanodomains on the plasma membrane of neurons and neuros

226 ermore, ARF1 and ARF3 localize to segregated nanodomains on the trans-Golgi network (TGN) and are fou

227 were controlled by Ca(2+) acting across two nanodomains, one between plasma membrane P/Q Ca(2+) chan

228 The TCR nanoclusters could array to form nanodomains or microdomains on the membrane of clonally

229 The functional significance of ordered nanodomains (or rafts) in cholesterol rich eukaryotic ce

230 The presence of DAG-generated nanodomains, or of DAG-induced lipid packing defects, is

231 es form membranes containing submicroscopic (nanodomain) ordered lipid domains (rafts).

232 Here, we review the current knowledge of nanodomain organization and function, with a particular

233 In this study, we explored the nanodomain organization of ribbon-type active zones by a

234 n together, our results reveal an unexpected nanodomain organization of synapses in which neurexin-1

235 onventional lipid-binding motif that confers nanodomain organization.

236 Flagellar Ca(2+) signaling nanodomains, organized by multi-subunit CatSper calcium

237 Furthermore, Flotillin 1 (Flot1), a nanodomain-organizing protein, associates with the kinas

238 H2O2 nanodomains originate from the mitochondrial cristae, wh

239 domain structure emerges in which elemental nanodomains, potentially capable of binding viruses, are

240 l decomposition starts by the formation of a nanodomain precursor state with a so-called tweed struct

241 Here we show that low-symmetry dynamic nanodomains present in the high-symmetry average cubic p

242 nal via receptor-associated independent cAMP nanodomains (RAINs) that constitute self-sufficient, ind

243 driven by these local endo-lysosomal Ca(2+) nanodomains rather than global cytoplasmic or ER Ca(2+)

244 As condensates age, nanodomains reposition, facilitating fused-in-sarcoma fi

245 Thus, ER-mitochondrial H2O2 nanodomains represent a component of inter-organelle com

246 bution of defects, for example in correlated nanodomains, requires characterization across length sca

247 ene end blocks phase separate into localized nanodomains, resulting in the formation of an optically

248 ignification specifically in this central CS nanodomain, revealing a nano-compartmentalized machinery

249 g ventricular myocyte intercalated disk (ID) nanodomains rich in cardiac sodium channels (Na(V)1.5) a

250 ting and depalmitoylating enzymes into AMPAR nanodomains segregated away from NMDAR nanodomains.

251 ordering of ferroelectric 109 degrees stripe nanodomains separated by periodic vertical domain walls

252 influence GLP-1R palmitoylation, clustering, nanodomain signaling, and internalization.

253 PSD95 expression level regulates AMPAR nanodomain size and compactness in parallel to miniature

254 self-quenching assays; and 4), evaluation of nanodomain sizes by time-resolved Forster resonance ener

255 Hierarchical assemblies of ferroelectric nanodomains, so-called super-domains, can exhibit exotic

256 phosphatidylserine (PtdSer) levels in ER/PM nanodomains, specified by the antagonistic action of the

257 We demonstrate that such synaptic gephyrin nanodomains stabilize the amplitude of inhibitory postsy

258 monstrate that the gephyrin rearrangement in nanodomains stabilizes the amplitude of postsynaptic cur

259 ired for both the establishment of perinexal nanodomain structure and the localization of both voltag

260 ut-of-plane direction and a peculiar rumpled nanodomain structure with very large variation in c/a ra

261 polarization and appearance of the MPB-like nanodomain structure.

262 gn, each pixel consists of properly arranged nanodomain structures capable of completely and dynamica

263 morphotropic phase boundary-like polymorphic nanodomain structures in chemically simple, lead-free, e

264 oscopy we find that ankyrin-G forms distinct nanodomain structures within the spine head and neck.

265 rroelectrics by enabling the manipulation of nanodomain structures, paving the way for developing rob

266 ut the physical basis of naturally occurring nanodomains such as lipid rafts.

267 xagonal close-packed structure embedded with nanodomains that adopt a vacated Barlow packing with ord

268 creating Ca(2+)-stabilized crystalline beta-nanodomains that cross-link and toughen the freshly draw

269 ell membranes consist of heterogeneous lipid nanodomains that influence key cellular processes.

270 scopy also reveal the presence of incoherent nanodomains that lithiate as if they are separate partic

271 Periodic nanodomains that self-organize into so-called 'superdoma

272 omplexes and the chain-restricting ionomeric nanodomains that they form.

273 orchestrated through a specialised endosomal nanodomain, the retrieval sub-domain.

274 precursors, contain carbon- and silica-rich nanodomains, the latter with extensive substitution of c

275 Syndapin I-enriched membrane nanodomains thus seem to be important spatial cues and o

276 ast cells, the relationship of ordered-lipid nanodomains to membrane topography had not been determin

277 erminal domain of Orai1 as central to Ca(2+) nanodomain-transcription coupling.

278 ethods are needed to detect and characterize nanodomains under normal membrane conditions.

279 ved the formation of low-polarity, raft-like nanodomains upon cholesterol addition or cholera-toxin t

280 partitioning of Ni(OEPone)(+) into the RTIL nanodomain was observed.

281 Moreover, within each nanodomain we observe extensive long range ordering of A

282 2Vdelta2 T cells bearing TCR nanoclusters or nanodomains were able to rerecognize phosphoantigen and

283 of controllable length with "patchy" coronal nanodomains were accessible.

284 ed in terms of the freezing of dynamic polar nanodomains where a high density of domain walls creates

285 tant diffusion is confined by distinct actin nanodomains where conformational changes required for Ja

286 eptors (AMPARs) are organized into so-called nanodomains where individual molecules are only transien

287 t cholesterol associates with PtdSer to form nanodomains where the headgroups of PtdSer are maintaine

288 GLP-1Rs into liquid-ordered plasma membrane nanodomains, which act as hotspots for optimal coordinat

289 orm aggregates leading to formation of lipid nanodomains, which are enriched in cholesterol, phosphat

290 ynamic partitioning into Lo-like proteolipid nanodomains, which encompass a major fraction of the mem

291 ing stabilizes flotillin1-associated ordered nanodomains, which in turn promote the nanoclustering of

292 rthermore, TADs are subdivided into discrete nanodomains, which persist in cells depleted of CTCF or

293 phosphodiesterase activity can organize cAMP nanodomains, while Zhao and coworkers find that protein

294 at estimate stationary single-channel Ca(2+) nanodomains with great accuracy in broad regions of para

295 re composed of small and dispersed chromatin nanodomains with lower DNA density compared to the large

296 rm highly hydrophobic and dynamically unique nanodomains, with extensive surface contacts to xylan.

297 dition of Ag to Cu in the form of segregated nanodomain within the same catalyst, synergistically acc

298 Cs co-organized with PSD-95, revealing MAGUK nanodomains within individual synapses containing either

299 eted activation of PKA and PKG at proteasome nanodomains would minimize the undesired effects from th

300 ntly confined within various plasma membrane nanodomains, yet how this may contribute to regulation o