ライフサイエンスコーパス: amphiphile

1 g a biologically inert, low-molecular-weight amphiphile.

2 ght of as monodisperse oligomers of a single amphiphile.

3 io-opaque elements encapsulated by synthetic amphiphile.

4 e achiral segment of the fluorescent peptide amphiphile.

5 s an effective and well-accessible colloidal amphiphile.

6 le by adjusting the structure of the polymer amphiphile.

7 rities and to self-assemble like a molecular amphiphile.

8 ecular self-assembly of a perylene monoimide amphiphile.

9 ntetheinyl transferase to generate a peptide amphiphile.

10 coil" and "globule-rod-coil" protein complex amphiphiles.

11 lar geometry, and hydrocarbon content of the amphiphiles.

12 erting the zwitterions into typical cationic amphiphiles.

13 f-assembled cylindrical micelles of cationic amphiphiles.

14 as a topological isomer pair of these shape amphiphiles.

15 ences from those characteristic of molecular amphiphiles.

16 d regulation of membrane protein function by amphiphiles.

17 bbon in supramolecular assemblies of peptide amphiphiles.

18 nded hydrophilic groups, affording polymeric amphiphiles.

19 uble monolayers of nonionic analogues of the amphiphiles.

20 the presence of DNA with the addition of the amphiphiles.

21 tric data on the membrane partition of other amphiphiles.

22 composed of hexagonal- and lamellar-forming amphiphiles.

23 igating the hydrophobic portions of cationic amphiphiles.

24 nanofiber formed by self-assembly of peptide amphiphiles.

25 self-assembling features of these dendritic amphiphiles.

26 can be preserved by using photocrosslinkable amphiphiles.

27 edia exhibit optical responses to biological amphiphiles.

28 e identical electronic properties of all PMI amphiphiles.

29 n of nanomaterials based on aromatic peptide amphiphiles.

30 A third, novel, LLC-forming, amphiphile 1-O-beta-(3,7,11,15-tetramethylhexadecyl)-d-r

31 f planar bilayers that contain two different amphiphiles, a lamellar former and a hexagonal former, w

32 lity, attributed to the unusual shape of the amphiphile: a relatively rigid molecule composed of a la

33 We report on a simple carbohydrate amphiphile able to self-assemble into nanofibers upon en

34 However, we find that anionic and cationic amphiphiles adopt strikingly different structures at liq

35 f a new class of cardanol-derived functional amphiphiles, along with their ability to generate hierar

36 A triple-helical "peptide-amphiphile" (alpha1(IV)1263-1277 PA), which binds CD44/C

37 Zwitterionic amphiphiles also can bind directly to the protein and en

38 molecular vaccines, through the synthesis of amphiphiles (amph-vaccines) comprising an antigen or adj

39 In binary systems consisting of an amphiphile and a solvent, the ability to tune the 3D cub

40 ne mesophases may form in select mixtures of amphiphile and solvent.

41 report here on the self-assembly of peptide amphiphiles and fatty acids driven primarily by anion-pi

42 groups increases the cohesion energy of the amphiphiles and favors the formation of two-dimensional,

43 mphiphiles, which thereby demix from neutral amphiphiles and form spots or rafts within vesicles as w

44 es (Sterosomes) formulated with single-chain amphiphiles and high content of sterols have been develo

45 polar and hydrophobic groups, such as ionic amphiphiles and proteins, is of paramount importance in

46 n vivo correlations that emphasize promising amphiphiles and successful formulation optimization effo

47 cation of an elastin-like protein by peptide amphiphiles and with the capacity to access, and be main

48 alently linked to the hydrophilic end of the amphiphile, and the second molecule is a shorter, nonflu

49 ith prescribed and well-defined densities of amphiphiles, and (iv) require only approximately 200 nL

50 utting of long CNTs in the presence of lipid amphiphiles, and for validation of CNTP incorporation in

51 nditions, these stimuli-responsive molecular amphiphiles are able to assemble into different structur

52 Dynamic amphiphiles are amphiphiles with dynamic covalent bridge

53 Enzyme-responsive peptide-polymer amphiphiles are assembled as spherical micellar nanopart

54 Tripod amphiphiles are designed to promote the solubilization a

55 Aromatic peptide amphiphiles are gaining popularity as building blocks fo

56 , we report that the same "fragrant" dynamic amphiphiles are ideal to screen for new siRNA transfecti

57 Ionic amphiphiles are known to stabilize the oil/water interfa

58 on hybrids, in which perylene diimide (PDI) amphiphiles are noncovalently immobilized onto single wa

59 MNG amphiphiles are promising tools for membrane protein sci

60 co-assembly arrangements of aromatic peptide amphiphiles are reviewed.

61 the aggregates formed in water by head/tail amphiphiles are revisited and discussed from the point o

62 These amphiphiles are soluble in aqueous solutions of triethan

63 High molecular weight ssDNA amphiphiles are synthesized by enzymatic polymerization.

64 ive phase behaviors of these molecular shape amphiphiles are unique and have not been systematically

65 urvival of vesicles composed of single chain amphiphiles as model protocell membranes.

66 , we report here the use of isomeric peptide amphiphiles as molecular building blocks to create one-d

67 e, the polymerization of monomers in peptide amphiphile assemblies by a rigid conjugated backbone als

68 r membranes to stabilize otherwise transient amphiphile assemblies.

69 that underpin the field of aromatic peptide amphiphile assembly, paving the way to a more rational d

70 neous mixture of assemblies when the peptide amphiphiles associate weakly with dodecanoic acid.

71 possible to draw firm conclusions regarding amphiphile association in solution from crystallographic

72 ar force probes to measure the net effect of amphiphiles, at concentrations often used in biological

73 hydrogen-bonding can induce such rigidity in amphiphile backbone.

74 ated a small library of structurally similar amphiphiles based on poly(2-oxazoline)s and poly(2-oxazi

75 Thus, aggregates of a prebiotic amphiphile bind certain heterocyclic bases and sugars, i

76 Contiguous cooperative amphiphile binding is predominantly driven by the hydrop

77 n transmitting the effect of the cooperative amphiphile binding to the i-face as a structural change

78 areful selection of LHGs, different types of amphiphiles (both polymer and small-molecule surfactants

79 Moreover, the serum half-life of the amphiphile bound to the cage and the protein was shown t

80 govern the self-assembly of aromatic peptide amphiphiles by focusing on four segments, (i) the N-term

81 Since each component of the amphiphile can be readily tailored, these micelles provi

82 rooctyl chain attached to a perylene diimide amphiphile can dramatically enhance the strength of supr

83 The effects of structurally diverse amphiphiles can be described by changes in a phenomenolo

84 ssumption that opportunely designed cationic amphiphiles can behave as CD14/MD-2 ligands and therefor

85 rane-mediated mechanisms by which biological amphiphiles can produce their cellular effects.

86 PEG-dendron amphiphiles can serve as powerful tools for the study of

87 Long fibers assembled from peptide amphiphiles capable of binding the metalloporphyrin zinc

88 s) represent the most recent self-assembling amphiphiles capable of forming monodisperse, stable, and

89 We found that these chromophore amphiphiles (CAs) self-assemble into charged nanostructu

90 owever, fusion is restored by the lipophilic amphiphile chlorpromazine or by the phospholipase C inhi

91 ctivity relationships were drawn within each amphiphile class, presenting the cellular and animal mod

92 To this end, the use of small molecules, amphiphiles, colloids, and polymers have been investigat

93 rticularly phospholipids and micelle-forming amphiphiles, commonly denoted detergents.

94 When the nonfluorescent peptide amphiphile component is designed to bind the important b

95 of pre-existing vesicles upon an increase in amphiphile concentration either through solvent evaporat

96 At low amphiphile concentrations above the critical aggregate c

97 echanisms that would lead to increased local amphiphile concentrations is an important aspect of defi

98 A C(s)-symmetric amide amphiphile containing a C(18) alkyl chain exists in at l

99 supramolecular assemblies of a novel peptide amphiphile containing aldehyde functionality in order to

100 One molecule is a fluorescent peptide amphiphile containing its branched stilbene chromophore

101 viously we showed that liposomes of cationic amphiphiles containing mannose-mimicking shikimoyl headg

102 repared from polymer-peptide block copolymer amphiphiles containing substrates for protein kinase A,

103 conjugates, small molecule prodrugs, or drug amphiphiles) could involuntarily aggregate, or self-asse

104 lves intercalation of the lipid tails of DNA amphiphiles (CpG motifs for TLR-9 stimulation) into the

105 Within 48h after amphiphile-CpG administration, immune activation could b

106 examined enhanced tumor-specific delivery of amphiphile-CpG, an albumin-binding analog of CpG ODN, fo

107 The amphiphile-decorated oil-water interfaces hosted within

108 Cationic amphiphiles derived from aminoglycosides (AGs) have been

109 fferent metals in the porphyrin ring for the amphiphiles described here) in variable proportions.

110 d and synthesized a novel class of glucoside amphiphiles, designated tandem malonate-based glucosides

111 f each PEG elastic spring so as to slow down amphiphile desorption.

112 Tripod amphiphiles differ from conventional detergents in that

113 The tetrahedrally shaped amphiphile displays an unprecedented aggregation behavio

114 A remarkable range of amphiphile-DNA structures (DNA-pyrene, DNA-triphenylphos

115 nanoporous network, whereas carboxylic acid amphiphiles do not adopt this nanoporous network due to

116 hydrogen-bonded beta-sheets, and chromophore amphiphiles driven to assemble by pi-orbital overlaps--w

117 e study of enzymatic hydrolysis of polymeric amphiphiles due to the monodispersity and symmetry of th

118 ation protocol, and the use of unique facial amphiphiles during crystallization.

119 by addition of both zwitterionic and neutral amphiphiles (e.g., diheptanoylphosphatidylcholine or Tri

120 sical properties change upon addition of new amphiphiles (e.g., lipids, alcohols, peptides, or protei

121 We introduce a class of amphiphiles, each built around a central quaternary carb

122 Within the hydrophobe-amphiphile efflux subfamily, these resistance-nodulation

123 means of two supramolecular systems--peptide amphiphiles engaged in hydrogen-bonded beta-sheets, and

124 water as the selective solvent, these shape amphiphiles exhibited versatile self-assembled micellar

125 The present bola-type supra-amphiphile exhibits strong fluorescence due to structura

126 tives of this maltose-neopentyl glycol (MNG) amphiphile family show favorable behavior relative to co

127 e developed a family of steroid-based facial amphiphiles (FAs) that are structurally distinct from co

128 led a Vroman-like competitive binding of the amphiphiles for the graphene oxide substrate.

129 ing for a way to rationally design dendritic amphiphiles for the last few decades.

130 s knowledge in the design of novel synthetic amphiphiles, formulations, and revolutionary screening a

131 producing a self-assembling aromatic peptide amphiphile from amino acid precursors that temporarily e

132 ynthesis of a homologous series of five such amphiphiles from 14 to 22 carbons-RNHCONHC(CH2CH2CO2H)3,

133 The self-assembly of biological amphiphiles has proved a fascinating topic in recent yea

134 e gas/water interface of cavitation bubbles, amphiphiles have an additional adsorptive flux.

135 Minimal self-reproducing amphiphiles have been developed in this context and as a

136 But amphiphiles have complex effects on the physical propert

137 Self-assembling dendritic amphiphiles have produced different nanostructures with

138 PFpP amphiphiles have therefore been prepared via an end grou

139 This study shows that biological amphiphiles have wide-ranging effects on plasma membrane

140 Heparin-binding peptide amphiphiles (HBPAs) self-assemble from aqueous media int

141 specific interactions between water and the amphiphile head groups, both at the interface and in the

142 imple expedient of mixing slightly different amphiphiles (i.e., different metals in the porphyrin rin

143 eins bind to and interact with the polymeric amphiphiles in both their assembled and monomeric states

144 ecently reported on the activity of cationic amphiphiles in inhibiting TLR4 activation and subsequent

145 measurements were performed on the discotic amphiphiles in mixtures of water and alcohol at temperat

146 nanostructures formed by charged chromophore amphiphiles in salt-containing aqueous solutions.

147 nducing properties of the promising cationic amphiphiles in syngeneic C57BL/6J mice under prophylacti

148 lateral phase separation of the two types of amphiphiles in the membranes.

149 eparation protocols to self-assemble peptide amphiphiles in water can result in the formation of diff

150 folded structure into soft matters formed by amphiphiles in water.

151 o understand the bilayer-modifying effect of amphiphiles (including therapeutic agents).

152 , we synthesize a series of methanofullerene amphiphiles, including derivatives of C60, C70, and C84,

153 rvature and, like other reversibly adsorbing amphiphiles, increase bilayer elasticity.

154 s of 1 nM, measured for PEO-rich bottlebrush amphiphiles, indicated an enhanced thermodynamic stabili

155 he induced circular dichroism signal of this amphiphile, indicating a sterically congested, but stabl

156 Amphiphile-induced changes in H(B), measured using gA ch

157 hat aggregates of decanoic acid, a prebiotic amphiphile, interact with the bases and sugar found in R

158 drophobic effect drives the self-assembly of amphiphiles into a broad range of micellar, rod-like, bi

159 The ability to direct the assembly of amphiphiles into a membrane creates new opportunities to

160 s, their modified versions, and other single amphiphiles into liposomes, and from block copolymers in

161 Self-assembly of peptide amphiphiles into nanostructures makes them attractive fo

162 stigations on the self-assembly of dendritic amphiphiles into various nanostructures in water on the

163 Also the peptide amphiphile investigated spontaneously nucleates the beta

164 e literature as to whether this single chain amphiphile is in fact bound by LFABP.

165 spontaneous formation of membranes from such amphiphiles is a concentration-dependent process in whic

166 formation of graphene derivatives by natural amphiphiles is essential for elucidating the biological

167 We show that four peptide amphiphile isomers, with identical composition but a dif

168 ing bilayer polymer membranes by adhesion of amphiphile-laden interfaces.

169 -ordered (Lo) and Ld domains among the three amphiphiles, leading to domain separation.

170 Our model accounts for amphiphile-level structural features, particularly hydro

171 The good solubility and molecular-amphiphile-like self-assembly properties can significant

172 guided to a large extent by the teachings of amphiphile (lipid or surfactant) self-assembly.

173 s been drawn between them, organic molecular amphiphiles (MAMs) and inorganic nanoparticle (NP) amphi

174 ness in three-dimensional artificial peptide amphiphile matrices offers a chemical strategy to contro

175 receptor (mouse sequence) preparation in an amphiphile membrane-like environment.

176 show that the 2D crystallization process in amphiphile membranes can be controlled by modifying the

177 on early Earth and other rocky planets, and amphiphile-mineral interactions in diverse other phenome

178 ows the renormalized bending stiffness of an amphiphile mixture membrane tube in contact with a flat

179 ures formed between tobramycin, DNA, and the amphiphile mixtures and show how interactions between th

180 ing cryogenic electron microscopy, a peptide amphiphile molecule containing aromatic residues was fou

181 eveloped a series of self-assembling peptide amphiphile molecules that transform either isolated from

182 Amphiphile molecules were prepared by attaching an aroma

183 embly of two model series of molecular shape amphiphiles, namely, hydrophilic [60]fullerene (AC(60))

184 y to study the molecular exchange of peptide amphiphile nanofibres, supramolecular systems known to h

185 Following self-assembly of peptide amphiphiles, nanoscale filaments form that display on th

186 synthetic cell-free therapy based on peptide amphiphile nanostructures designed to mimic the activity

187 hiles (MAMs) and inorganic nanoparticle (NP) amphiphiles (NPAMs) are significantly different in dimen

188 Activation by amphiphiles occurs with both micellar (phosphatidylinosi

189 olecule is a shorter, nonfluorescent peptide amphiphile of complementary charge.

190 We report here on an amphiphile of completely different chemistry based on az

191 ful linkers for the synthesis of macrocycles/amphiphiles of complementary chirality.

192 c surfactant molecules, representing anionic amphiphiles of endocytic membranes.

193 We conclude that self-assembling amphiphiles of lysine-rich RSH extensin form positively

194 ics, n-alcohols are perhaps the best-studied amphiphiles of this class.

195 Here we show that anionic and cationic amphiphiles of unequal charge can coassemble into small

196 ssembling dilysine (+2) and carboxylate (-1) amphiphiles of various tail lengths into bilayer membran

197 The solution self-assembly of macromolecular amphiphiles offers an efficient, bottom-up strategy for

198 erative sequential and contiguous binding of amphiphiles on the i-face.

199 o lead to quantitative transfer of insoluble amphiphiles onto the oil-water interfaces.

200 mixtures of cationic and negative curvature amphiphiles optimized for DNA binding via charge matchin

201 ertion of cone-shaped or inverse cone-shaped amphiphiles or by cholesterol removal switches CD39 to t

202 The amide amphiphiles overcome the barrier to symmetry generation

203 eport here on a coassembly system of peptide amphiphile (PA) molecules designed to form nanofibers fo

204 Peptide amphiphile (PA) molecules that self-assemble in vivo int

205 ane disruption was integrated into a peptide amphiphile (PA) that self-assembles into bioactive, cyli

206 self-assembly of mixtures of bilayer-forming amphiphiles, particularly phospholipids and micelle-form

207 The predictive powers should extend also to amphiphile partitioning and the kinetics of lipid-monome

208 Peptide amphiphiles (PAs) are a class of amphiphilic molecules a

209 Recent evidence indicates that peptide amphiphiles (PAs) are promising candidates for use as ma

210 ramolecular liquid crystal formed by peptide amphiphiles (PAs) that encapsulates cells and growth fac

211 on a set of diacetylene-derivatized peptide amphiphiles (PAs) that react to form conjugated polydiac

212 ilic packing in the self-assembly of peptide-amphiphiles (PAs) was investigated using a series of 26

213 We synthesized a series of peptide amphiphiles (PAs) with systematically modified amino aci

214 ment of tumors using self-assembling peptide amphiphiles (PAs).

215 tics and activities of the resulting peptide amphiphiles (PAs).

216 ater in driving the self-assembly of peptide amphiphiles (PAs).

217 These end-attached PNA amphiphiles (PNAA) partition to nonionic micelles in the

218 In summary, these nonlipid amphiphiles provide new tools to tune domain formation i

219 alent ligands within a mixture of polyvalent amphiphiles provides, in principle, a simple mechanism f

220 perties of aqueous micelles derived from the amphiphile PTS are described.

221 tion of membrane proteins by drugs and other amphiphiles remains unknown.

222 lf-assembly of molecular and block copolymer amphiphiles represents a well-established route to micel

223 expressed by the minimum volume fraction of amphiphile required to form microemulsion (Phi(ME)), whi

224 e on a proof-of-concept bioconjugate polymer amphiphile, revealed growth and evolution occurring by u

225 inding chemistry to design a new fluorinated amphiphile, RfNTA, using an improved one-step synthesis

226 y grafted with macromolecules ('nanoparticle amphiphiles') robustly self-assemble into a variety of a

227 er membranes composed of simple single-chain amphiphiles seem to be well-suited for a potential role

228 Amphiphile selection is a critical step for structural s

229 he ability of ionic liquids (ILs) to support amphiphile self-assembly into a range of mesophase struc

230 tructures that are formed, and (iii) how can amphiphile self-assembly materials be used to enhance pr

231 Ordered amphiphile self-assembly materials with a tunable three-

232 In this review we discuss ionic liquids as amphiphile self-assembly media, and identify trends that

233 To reproducibly engineer the low energy amphiphile self-assembly of materials for the future, we

234 e ionic liquid and its characteristics as an amphiphile self-assembly solvent has been found.

235 ast that many more ILs will be identified as amphiphile self-assembly solvents in the future.

236 ecent key findings regarding (i) what drives amphiphile self-assembly, (ii) what governs the self-ass

237 Molecular amphiphiles self-assemble in polar media to form ordered

238 Owing to their "dual" affinity, amphiphiles self-assemble in water to form different kin

239 re morphologies resulting from the dendritic amphiphiles' self-assembly.

240 ructures obtained from natural and synthetic amphiphiles serve as mimics of biological membranes and

241 uman aortic endothelial cells with exogenous amphiphiles, shown previously in model membranes, and co

242 EC50 ratios for two commercial amphiphiles, sodium dodecyl sulfate (SDS) and Triton X-1

243 hese results suggest that optimized cationic amphiphile solutions have the potential to enhance antim

244 antages of cholesterol with those of charged amphiphiles, stabilizing the aligned phase and preventin

245 hat vesicles composed of simple single-chain amphiphiles such as fatty acids, fatty alcohols, and fat

246 his study we systematically examined whether amphiphiles such as indomethacin influence Ras protein n

247 levels and high concentrations of exogenous amphiphiles, suggesting it as a general feature of the o

248 The results reported here show that peptide amphiphile supramolecular systems can be dynamic and tha

249 The third-generation designer amphiphile/surfactant, "Nok" (i.e., SPGS-550-M; beta-sit

250 ithin the same energy landscape, the peptide-amphiphile system forms a thermodynamically favoured pro

251 Many cationic amphiphiles tested positive, and some targeted isoprenoi

252 rylated once more to generate a farnesyl-CoA amphiphile that self-assembles into spherical micelles.

253 in aqueous media produces a bola-type supra-amphiphile that self-assembles to produce higher order m

254 LPS is an amphiphile that spontaneously inserts into the outer lea

255 These results demonstrate that only the amphiphile that thinned Ld lipid domains increased beta1

256 his aggregate consists of three inequivalent amphiphiles that assemble to create 3- and 6-fold rotati

257 are designing novel cationic and procationic amphiphiles that can pack, transport, and deliver nuclei

258 rticles are colloidal analogues of molecular amphiphiles that can self-assemble to form diverse supra

259 work is motivated by one class of molecular amphiphiles that change their surfactant properties in r

260 Antimicrobial peptides (AMPs) are cationic amphiphiles that comprise a key component of innate immu

261 ort the crystal structures of several tripod amphiphiles that contain an N-oxide hydrophilic group.

262 s, we prepared a small collection of anionic amphiphiles that could recognize cations by ionpair-pi i

263 d evaluation of a new class of benzothiazole amphiphiles that exhibit a dose-dependent response leadi

264 gating dendritic alkyl chains to DNA creates amphiphiles that exhibit high-affinity (Kd in low nanomo

265 protocell membranes because they are simple amphiphiles that form bilayer membrane vesicles that ret

266 Antimicrobial peptides are small cationic amphiphiles that play an important role in the innate im

267 We present thrombin-binding aptamer amphiphiles that self-assemble into nanoscale polymeric

268 convert nonstructure forming molecules into amphiphiles that spontaneously assemble into vesicles.

269 Many drugs are amphiphiles that, in addition to binding to a particular

270 intermolecular complexes can exist for this amphiphile, the molecule folds into a unique intramolecu

271 n the dimension mismatch of the two types of amphiphiles, the entanglement of polymer chains, and the

272 In contrast to activation by amphiphiles, the rate enhancement by salt occurs for onl

273 Different from conventional amphiphiles, these hybrids show pH-dependent and counter

274 ed by rational design in the headgroup of an amphiphile to generate small micelles with enhanced stab

275 The ability to utilize multiple distinct amphiphiles to construct discrete assemblies represents

276 PEG chain induces self-assembly of polymeric amphiphiles to form micrometer-sized vesicles entrapping

277 The presence of zwitterionic and neutral amphiphiles (to which the protein binds weakly) dilutes

278 on of n-alkylated peptide nucleic acids (PNA amphiphiles) to the products, followed by separation wit

279 presence of zinc powder, aided by a nonionic amphiphile, to give the alkylated aromatic.

280 those based on either natural or fluorinated amphiphiles, to polymer-based ones.

281 The pathway by which amphiphiles transform from an initial state of vesicles

282 Anionic amphiphiles, U73343 (a less electrophilic U73122 analogu

283 xtures under the influence of three nonlipid amphiphiles, vitamin E (VE), Triton-X (TX)-100, and benz

284 Here, we show that simple amphiphiles/water systems reproduce this behavior, which

285 nd charged oligo(p-phenylene vinylene) (OPV) amphiphiles were fabricated in one step by spin casting

286 tizing perylene monomimide (PMI) chromophore amphiphiles were found to show variation in hydrogen gas

287 or spectroscopic investigation is to form an amphiphile, which is able to disperse the latter at the

288 D in toxicity induced by U18666A, a class II amphiphile, which triggers cell death by impairing the t

289 ns are shown here to crossbridge polyanionic amphiphiles, which thereby demix from neutral amphiphile

290 Here we report that GO is an amphiphile with hydrophilic edges and a more hydrophobic

291 A quaternary amphiphile with swallow-tail side groups displays a new

292 We describe cholate-based cage amphiphiles with a unique architecture that combines ele

293 c function of perylene monoimide chromophore amphiphiles with different alkyl linker lengths separati

294 Dynamic amphiphiles are amphiphiles with dynamic covalent bridges between their

295 on (1)H-(13)C HSQC experiments, complexes of amphiphiles with more than 10 different maltooligosaccha

296 dispersities were obtained from bottlebrush amphiphiles with packing parameters of approximately 0.3

297 functionalized polymer to give rise to shape amphiphiles with precisely defined surface chemistry and

298 versus fibers) in a series of simple peptide amphiphiles with the sequence c16-xyL3K3-CO2H where c16

299 hed dendrons make an excellent headgroup for amphiphiles with ultralong, saturated, linear alkyl chai

300 ebiotic synthesis of fatty acids and related amphiphiles would result in dilute solutions well below