ライフサイエンスコーパス: amphiphile

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

2 ecular self-assembly of a perylene monoimide amphiphile.

3 ntetheinyl transferase to generate a peptide amphiphile.

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

5 io-opaque elements encapsulated by synthetic amphiphile.

6 ght of as monodisperse oligomers of a single amphiphile.

7 le by adjusting the structure of the polymer amphiphile.

8 s an effective and well-accessible colloidal amphiphile.

9 formations are prevalent for A blocks of BAB amphiphiles.

10 edia exhibit optical responses to biological amphiphiles.

11 rplays among three components of the T-shape amphiphiles.

12 e identical electronic properties of all PMI amphiphiles.

13 n of nanomaterials based on aromatic peptide amphiphiles.

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

15 lar geometry, and hydrocarbon content of the amphiphiles.

16 erting the zwitterions into typical cationic amphiphiles.

17 les from a range of crystallizable polymeric amphiphiles.

18 f-assembled cylindrical micelles of cationic amphiphiles.

19 les from a range of crystallizable polymeric amphiphiles.

20 as a topological isomer pair of these shape amphiphiles.

21 ences from those characteristic of molecular amphiphiles.

22 d regulation of membrane protein function by amphiphiles.

23 bbon in supramolecular assemblies of peptide amphiphiles.

24 nded hydrophilic groups, affording polymeric amphiphiles.

25 oton motive force, similar to other cationic amphiphiles.

26 nanofiber formed by self-assembly of peptide amphiphiles.

27 s consisting of proapoptotic peptide-polymer amphiphiles.

28 self-assembling features of these dendritic amphiphiles.

29 can be preserved by using photocrosslinkable amphiphiles.

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

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

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

33 ies formed by synthetic alkyl triazole-based amphiphiles against interfaces of thermotropic liquid cr

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

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

36 However, these amphiphiles also carry a "nucleotide code" such that sub

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

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

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

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

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

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

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

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

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

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

47 drimers, polyvalent metals, metal complexes, amphiphiles, and alkaloids allow tailoring properties fo

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

49 o constitutionally isomeric aromatic peptide amphiphiles (APAs), K(S)C'EK(S) and C'EK(S)K(S) (K(S) =

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

51 Dynamic amphiphiles are amphiphiles with dynamic covalent bridge

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

53 Tripod amphiphiles are designed to promote the solubilization a

54 Aromatic peptide amphiphiles are gaining popularity as building blocks fo

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

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

57 These multiacylated lipid amphiphiles are molecular patterns that are differential

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 ally well-segregated yet the B blocks of ABA amphiphiles are significantly less stretched than in the

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 ermolysin-responsive peptide-based polymeric amphiphiles assembled into spherical micellar nanopartic

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 paper unmask new nonequilibrium behaviors of amphiphiles at LC interfaces, and provide fresh approach

73 d that collision and subsequent spreading of amphiphiles at the interface generates a surface pressur

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

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

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

77 Ranging from 2D assemblies to peptide amphiphile-based biomaterials, Prof.

78 The self-assembly of these amphiphiles bears some similarities, but also some diffe

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

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

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

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

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

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

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

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

87 or explorations into how nonnatural membrane amphiphiles can be used to both study and enhance the pr

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

89 Bilayers of amphiphiles can organize into spherical vesicles, nanotu

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

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

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

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

94 We designed amphiphile CAR-T ligands (amph-ligands) that, upon injec

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

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

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

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

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

100 At low amphiphile concentrations above the critical aggregate c

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

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

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

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

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

106 Ionic amphiphiles containing two imidazolium rings close to ea

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

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

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

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

111 Cationic amphiphiles derived from aminoglycosides (AGs) have been

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

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

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

115 Tripod amphiphiles differ from conventional detergents in that

116 The tetrahedrally shaped amphiphile displays an unprecedented aggregation behavio

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

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

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

120 of bulky, membrane-disruptive supramolecular amphiphiles due to "too strong" binding of anions to tri

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

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

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

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

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

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

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

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

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

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

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

132 Due to the restricted rotation, the amphiphiles feature "double" atropisomeric axes in their

133 A novel hybrid bioinspired amphiphile featuring a cytosine moiety, which self-assem

134 tional basis for the design of lipid-polymer amphiphiles for optimized lymphoid targeting.

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

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

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

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

139 s generated inside the monolayer and attacks amphiphiles from a lateral direction.

140 ylene glycol) (PEG)-pyropheophorbide-a (Ppa) amphiphiles (G320P, G310P, G220P, and G210P) are synthes

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

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

143 tocells derived from phospholipids and other amphiphiles have been made and their enzymatic-driven mo

144 But amphiphiles have complex effects on the physical propert

145 Self-assembling dendritic amphiphiles have produced different nanostructures with

146 PFpP amphiphiles have therefore been prepared via an end grou

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

148 id side-chains along the PNA backbone yields amphiphiles having a "protein code" that directs self-as

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

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

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

152 he development of diagnostics, and learn how amphiphiles in general use lipid trafficking to navigate

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

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

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

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

157 h the assembly of T-shape polymer-rod-sphere amphiphiles in the bulk state.

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

159 dictates the kinetics and structures of the amphiphiles in the organic phase as they decorate the in

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

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

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

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

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

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

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

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

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

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

170 Also the peptide amphiphile investigated spontaneously nucleates the beta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 Amphiphile molecules were prepared by attaching an aroma

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

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

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

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

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

194 Activation by amphiphiles occurs with both micellar (phosphatidylinosi

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

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

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

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

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

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

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

202 noclusters without the use of any additional amphiphiles or carriers.

203 , we designed a series of symmetric triblock amphiphiles (or high-chi block oligomers) comprising inc

204 The amide amphiphiles overcome the barrier to symmetry generation

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

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

207 Here, a charged, chiral amphiphile (palmitoyl-lysine, C(16)-K(1)) is used to elu

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

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

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

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

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

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

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

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

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

217 Cell-like hybrids from natural and synthetic amphiphiles provide a platform to engineer functions of

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 Vesicles formed from single-chain amphiphiles (SCAs) such as fatty acids probably played a

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

229 Amphiphile selection is a critical step for structural s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 Nonnatural amphiphiles, such as diblock copolymers, provide an inte

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

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

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

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

250 low as 1.0 using mixed surfactant or polymer-amphiphile systems with significant positive charge/numb

251 Many cationic amphiphiles tested positive, and some targeted isoprenoi

252 erapy, here we test a synthetic VEGF peptide amphiphile that self-assembles into nanoparticles.

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

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

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

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

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

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

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

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

261 e have assembled a series of nanosized shape amphiphiles that comprise a triphenylene core and six po

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

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

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

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

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

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

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

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

270 In lamellae formed by ABA amphiphiles, the fraction of B blocks "bridging" adjacen

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

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

273 PRAS), nanostructured liquids generated from amphiphiles through sequential self-assembly and coacerv

274 f-assembly and physicochemical properties of amphiphiles, thus affecting their biological effects.

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

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

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

278 d by the addition of suitably functionalized amphiphiles to the droplets.

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

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

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

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

283 Anionic amphiphiles, U73343 (a less electrophilic U73122 analogu

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

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

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 interactions of supramolecular assemblies of amphiphiles with fluid interfaces at the single-event le

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

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

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

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

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