ライフサイエンスコーパス: monomer

1 ipid vesicles, QUAD opsin reconstitutes as a monomer.

2 resulting in reduced compactness of the PepQ monomer.

3 A at nicks, abasic (AP) sites, and ends as a monomer.

4 that BAM2 was a tetramer, whereas BAM5 was a monomer.

5 DIBAL-H structures into their more reactive monomer.

6 elongation after insertion of a fluorinated monomer.

7 nd that A3G first transiently binds DNA as a monomer.

8 , it was believed to operate as a functional monomer.

9 Pases, ATP7B is assumed to be a single-chain monomer.

10 uncleaved pseudotrimer and the matched gp120 monomer.

11 rent perfluorinated or highly activated aryl monomers.

12 aS fibrils resist incorporation of WT-alphaS monomers.

13 s existing at various feed ratios of the two monomers.

14 the achiral (soldier) and chiral (sergeant) monomers.

15 ugh head-to-tail interactions of the bipolar monomers.

16 CR localizations, which likely represent BCR monomers.

17 pha-subunits are believed to form functional monomers.

18 al switch can occur independently in the two monomers.

19 inclusion of terminal alkyne groups in these monomers.

20 were completely consistent with those of the monomers.

21 of HSA molecules with appropriate functional monomers.

22 ader combinations of prebiotically plausible monomers.

23 mixed oligomers composed of NtBu and Ns1tbe monomers.

24 conjoined half-sites preferred by partnering monomers.

25 ng to measure interactions between NM myosin monomers.

26 Cer), without apparent disassembly into free monomers.

27 om a 1:1 mixture of (13)C- and (15)N-labeled monomers.

28 r-loaded gel core is placed in a solution of monomer 1.

29 ity (1.58 cm(2)V(-1)s(-1)) compared the DMMP monomer (1.63 cm(2)V(-1)s(-1)).

30 is loaded with fresh initiator and placed in monomer 2, which causes a concentric shell of polymer 2

31 A thymidine-derived bicyclic monomer, 3',5'-cyclic 3-(3-butenyl) thymidine ethylphosp

32 Monomers (5 Si atoms/molecule) and dimers (10 Si atoms/m

33 new leaving group significantly accelerates monomer addition as well as trimer-assisted RNA primer e

34 situ block copolymerization upon sequential monomer addition for the case of methacrylates and styre

35 was sufficient to support PU.1 binding as a monomer, additional flanking bases were required to invo

36 We have synthesized 15 new spiroligomer monomer amines that contain two stereocenters and three

37 osed in a capsid with one maturation protein monomer and 89 coat protein dimers arranged in a T = 3 i

38 of CysC therefore likely initiates from the monomer and does not require domain-swapping.

39 g methacrylic acid or methyl methacrylate as monomer and ethylene glycol dimethacrylate as cross-link

40 dues in this peptide compared to that of the monomer and in the bulk solution.

41 eased, suggesting that TP2 translocates as a monomer and is inhibited by lateral interactions in the

42 t physiological concentrations c-di-GMP is a monomer and little is known about how higher oligomeric

43 vel intercalated complex for the hairpin and monomer and Monte Carlo modeling further demonstrated th

44 Both monomer and polymer single crystals are analyzed by X-ra

45 G expression, the overall abundance of ISG15 monomer and protein conjugates rises in HCMV-infected ce

46 Additionally, an equimolar mixture of the monomer and the hairpin assembles into non-fibrillar agg

47 differ significantly from the spectra of the monomer and trimer.

48 PfVIT purified as a monomer and, as measured by intrinsic protein fluorescen

49 quilibrium of multivalent ureidopyrimidinone monomers and a monovalent naphthyridine molecule which a

50 RA currently focuses on monomers and additives used in the manufacture of produc

51 he same overall structure of native TGF-beta monomers and bound TbetaRII in an identical manner.

52 ion of HOMs characterized as C8-10H12-18O4-9 monomers and C16-20H24-36O8-14 dimers in alpha-pinene de

53 ctin filament assembly by sequestering actin monomers and capping filament barbed ends.

54 uggested that Abeta(1-42) oligomers, but not monomers and fibers, formed three distinct pore structur

55 Flavanol monomers and glucoside conjugates were not recovered in

56 llowing the electrokinetic movement of DS(-) monomers and micelles into the capillary.

57 t polyphenols were flavan-3-ols, flavan-3-ol monomers and oligomers, with an average degree of polyme

58 thermal polymerization of methacrylate-based monomers and the photopolymerization of methyl methacryl

59 y, Watson-Crick base pairing between the RNA monomers and the template is observed at the extension s

60 ation between bisalkylsulfonyl fluorides (AA monomers) and bisphenol bis(t-butyldimethylsilyl) ethers

61 d monomers, trisolvated dimers, octasolvated monomers, and octasolvated dimers were identified.

62 tiates the polymerization of the vinyl ether monomer-and a dithiocarbamate radical that is likely in

63 e prodomain arm domain and GF domain in each monomer are swapped).

64 lity, and availability of benzophenone imine monomers are all attractive features of this approach.

65 s into straight filaments in which flagellin monomers are arranged in a left-handed helix.

66 merization reactions, mostly multifunctional monomers are employed, as they ensure fast reaction time

67 mposite resins that contain special adhesive monomers are necessary.

68 er follows a first-order process where lipid monomers are transferred presumably through the aqueous

69 ization rates, implying that the majority of monomers are transiently kept in a non-polymerizable "re

70 mics predict a general rigidification of the monomer as compared to wild-type.

71 of trimeric photosystem I (PSI) and two PSII monomers as deduced from electron microscopy.

72 apable of multimerization, leading to excess monomers at vesicle membranes.

73 vibronic structure is quenched as the water monomer becomes electronically perturbed.

74 d in the virion first deaminate viral DNA as monomers before dimerizing to form multiple enzymaticall

75 , demonstrate a stoichiometry of one Delta22-monomer binding to every two consecutive GGAA-repeats on

76 into the amyloid fibril: namely, the initial monomer binding to the fibril end (charge-dependent, rel

77 inositide PI(3,4,5)P3 and involves the actin monomer-binding protein profilin.

78 ymerization, with nanoparticles as linkable "monomers"; bond angles determined by directional interna

79 ciations involving four polymerized cationic monomers bonded to two different polymer chains.

80 The boroxole functional monomer bound the sugar templates through cis-1,2-diol,

81 one monomer on the G4 strand and the second monomer bound to the C-rich strand.

82 res of FAM3C ILEI and show that it exists as monomers but also as covalent dimers.

83 dominant ADCP activity of anti-gp41 against monomers but not trimers, with some higher activity of a

84 We found that CLEC3A mainly occurs as a monomer, but also forms dimers and trimers, potentially

85 A method for 18 phenolic monomers by HPLC-DAD was developed, validated, and appli

86 he hypothesis that the strained 3',5'-cyclic monomer can promote ring-opening polymerization to affor

87 We conclude that an engineered opsin monomer can scramble phospholipids, and that the lipid-e

88 of G structural changes and suggests that G monomers can re-associate, through antiparallel interact

89 RAS-independent and signal either as active monomers (class 1) or constitutively active dimers (clas

90 on by the FRP, a different oligomeric state (monomer compared to dimer for OCP1) and lower fluorescen

91 on the use of covalent bond formation among monomers, compensating for intermolecular electrostatic

92 terocyclic diamidine, DB2277, forms a strong monomer complex with a DNA sequence containing 5-AAAGTTT

93 tion and formation of a 1:1:1 NEIL1-DNA-PCNA(monomer) complex.

94 studies reveal that the stability of hairpin-monomer complexes is much higher than hairpin-hairpin co

95 erized by mass spectrometry to determine its monomer composition.

96 We now show that the differences in myosin monomer concentration of RLC-unphosphorylated and -phosp

97 of magnitude higher than the in vitro actin monomer concentration required to support the observed p

98 es the high CMC of surfactant precludes high monomer concentration within micelles.

99 ith the LBD enables CAR to adapt a transient monomer configuration that can be converted to either th

100 in structure, consisting of two Abeta(14-23) monomers connected by a turn forming YNGK peptide.

101 It is a homotetramer, with each monomer consisting of a transmembrane region, a stalk, a

102 Each CHIP monomer consists of a tetratricopeptide-repeat (TPR), he

103 data, concentration of active catalyst, and monomer consumption suggests optimal activation conditio

104 face, which facilitates grafting and reduces monomer consumption.

105 Thus, the homodimer-monomer conversion is the underlying molecular mechanism

106 rization mechanism, and only low to moderate monomer conversions were attained.

107 pin-free system in which double-stranded DNA monomers could dendritically assemble into highly branch

108 monomers show a large change in density when monomers covalently join in polymer chains.

109 f two new selenophene-containing ladder-type monomers, cyclopentadiselenophene (CPDS) and indacenodis

110 s into large clusters containing hundreds of monomers dampens the signaling.

111 ling, here the authors show that local actin monomer depletion and network architecture can tune the

112 ct solution conformation of polymers through monomer design.

113 ride polymers, dimers, oxidized triglyceride monomers, diglycerides and free fatty acids, and inducti

114 orms monomers upon GTP binding, leading to a monomer-dimer cycle during GTP hydrolysis.

115 Moreover, the monomer-dimer equilibrium affinity constant was determin

116 SecA has been shown to exist in a dynamic monomer-dimer equilibrium modulated by translocation lig

117 hentic HIV RNA is regulated independently of monomer:dimer equilibrium of the 5'UTR.

118 show that G12V K-Ras exists as a mixture of monomers, dimers and larger oligomers, while the K101E m

119 of the dephosphorylated filaments to folded monomers, dimers, and small oligomers, followed by diffu

120 IN precursors are monomers, dimers, or tetramers in solution.

121 different oligomeric assemblies ranging from monomers, dimers, tetramers to higher order oligomers to

122 R revealed an asymmetric homodimer, with one monomer displaying complete regulatory metal coordinatio

123 ion of Hyp fluorescence originating from Hyp monomers dissolved in the GUV membrane has been recorded

124 nts, but involves the key assumption that gA monomers do not exchange between bilayers.

125 ound that small structural variations in the monomers dramatically affected the crystallinity, surfac

126 of 14-3-3zeta is a consequence of the dimer-monomer dynamics and may play a role in conferring chape

127 role of FP oligomerization in vivo while our monomers enable detailed structural insight paving the w

128 t measurably enhancing beta-structure in the monomer ensemble.

129 he experimental observations, revealing that monomer exchange in and out the fibres originates from t

130 erfering with H-bonding to the next incoming monomer exhibit poor amyloid formation and act as potent

131 like DNA-binding conformation and the second monomer exhibiting disrupted regulatory metal coordinati

132 The other two constructs, an exact monomer flanked by ribozymes and a trihelix-forming RNA

133 Hydroxycinnamic acids, flavan-3-ol monomers, flavonols and anthocyanins leached in the syru

134 ation of cyclically docked arrangements of a monomer followed by sequence design of the newly formed

135 The helical domains of each Cya monomer form a tight hairpin, bringing the two catalytic

136 not only in the classical heteropentameric "monomer" form, but that it also adopts much larger confi

137 ess cytosolic actin assembly prevented actin monomer from rapid translocation to and efficient incorp

138 ends, and (ii) promoting shuttling of actin monomers from profilin-actin complexes onto nearby WH2 d

139 ging photophysical states of individual C-PC monomers from Spirulina platensis in free solution by si

140 different benzene-1,3,5-tricarboxamide (BTA) monomers functionalized with either oligodimethylsiloxan

141 port that spatiotemporal enrichment of actin monomers (G-actin) in dendritic spines regulates spine d

142 t was particularly notable for a hydrophobic monomer glycidyl methacrylate combined with a nonionic s

143 cursor and N-dodecyl imidazole as functional monomer, gold nanoroots (AuNRs) were fabricated and char

144 Each monomer has flexible loop regions linking the core alpha

145 Antimicrobial and ester-free monomers have been developed in the recent past, and evi

146 Here, we measured APJ monomer-homodimer-oligomer interconversion by monitoring

147 In both Abeta protofibrils and monomers, HSA targets key Abeta self-recognition sites s

148 way to the PTS1 import pathway supports Gpd1 monomer import but not Gpd1 homodimer import and Pnc1 co

149 These studies identify a role of p40 monomer in helping cancer cells to escape cell death via

150 aphy showed two juxtaposed FAD molecules per monomer in redox communication with an active disulfide

151 ve conformations adopted by a folded insulin monomer in solution, namely, the R-, the R(f)-, and the

152 ttering experiments, revealed that ObgE is a monomer in solution, regardless of the bound nucleotide.

153 ar homogeneity and found that it exists as a monomer in solution.

154 t interacts with the arm domain in the other monomer in the dimeric structure (i.e. the prodomain arm

155 : see text]) and polar ([Formula: see text]) monomers in a computational model.

156 ing experiments verified that individual BSA monomers in bulk solution had increasingly lower conform

157 s of tNTPs, will help advance the use of TNA monomers in exobiology and biotechnology applications.

158 (i) bringing polymerization-competent actin monomers in proximity to growing filament ends, and (ii)

159 henylene and 1,4-phenylene bis(boronic acid) monomers in solution.

160 ared by simply changing the functional vinyl monomers in the polymerization mixture.

161 ing-opening polymerization of several common monomers, including lactide, delta-valerolactone, epsilo

162 ypically depresses catalytic activity and co-monomer incorporation.

163 n of nonaromatic 5,5-dimethylcyclopentadiene monomer into a conjugated backbone is an attractive stra

164 usion distance of unreacted cross-linker and monomer into a prepolymerized hydrogel sink results in a

165 rt polycrystalline or single-crystal benzene monomer into single-crystalline packings of carbon nanot

166 the activation of the receptor by assembling monomers into 6- to 8-mer oligomers; condensation of the

167 s preventing the reorganization of E protein monomers into fusogenic trimers in the acidic environmen

168 wo steps of incorporation of alpha-synuclein monomers into the amyloid fibril: namely, the initial mo

169 From these analyses, we show that the monomer is intrinsically disordered and that the dimer c

170 nstrate that the prodomain arm domain in one monomer is linked to the GF that interacts with the arm

171 erization of ethylene with functionalized co-monomers is a long-sought-after approach to introducing

172 -specific, because the HSA affinity of Abeta monomers is lower for Abeta(1-42) than for Abeta(1-40).

173 lar Abeta, but the affinity of HSA for Abeta monomers is lower than for Abeta protofibrils (Kd values

174 The low affinity observed for GCRho monomers is unusual for this enzyme class and suggests t

175 Herein, we describe an engineered TGF-beta monomer, lacking the heel helix, a structural motif esse

176 The isolated protein, a 45-kDa monomer, lacks catalytic activity but becomes active upo

177 Its dissociation into monomers leads to the formation of fibrils that underlie

178 ential association that is determined at the monomer level.

179 They show that actin monomer levels are elevated in spines upon activity, wit

180 arameters: Starting as a nucleation site for monomer-monomer contacts, this six-residue sequence elem

181 (N-isopropyl acrylamide) (PNIPAM) and in its monomer N-isopropyl acrylamide (NIPAM) in solution acros

182 The third interface between Hda monomers occludes the active site arginine finger, block

183 Tracheal cytotoxin (TCT), a monomer of DAP-type peptidoglycan from Bordetella pertus

184 disulfide bond is easily formed between the monomers of the dimer preventing carotenoid transfer.

185 f residues located at key interfaces between monomers of this RBM resulted in severe defects both in

186 a hexanuclear cluster structure wherein two monomer-of-trimer units are linked by a genuine d(10)-d(

187 ted the average translocation rate of a UvrD monomer on ssDNA composed solely of deoxythymidylates.

188 re a PC4 dimer accommodates the DNA with one monomer on the G4 strand and the second monomer bound to

189 equence-controlled hydrophobic and ionizable monomers on the inner surface of solid-state nanopore.

190 stabilizing hydrogen bonds between the PsbS monomers only at high lumen pH, whereas at low pH (exces

191 e loop; and Form 4 is a zero-nucleotide loop monomer or an interlocked dimer.

192 ely, materials composed of a trimethacrylate monomer or bisphenol A glycidyl methacrylate, which is a

193 biquitin is ligated to substrate proteins as monomers or chains and the topology of ubiquitin modific

194 -opened species are much less prevalent than monomers or dimers and the aerosol yield is higher.

195 though most transcription factors operate as monomers or dimers, a few, including the E26 transformat

196 s binds a single sequence-specific site as a monomer over a single helical turn.

197 tic response depends on the structure of the monomer, polymer molecular weight and concentration, and

198 FtsZ monomers polymerize head to tail forming tubulin-like dy

199 stereomutation was observed only if the CBI monomer possesses molecular pockets.

200 ia self-sorting behavior among three sets of monomers possessing mismatched host-guest pairs.

201 a self-sorting behavior among three sets of monomers possessing mismatched host-guest pairs.

202 Here we show that Bri2 BRICHOS monomers potently prevent neuronal network toxicity of A

203 eact, with the steric bulk of the functional monomers preventing the favorable Lewis acid base intera

204 C-terminal growth factor (GF) domain in each monomer, pro-TGF-beta is secreted and stored in latent c

205 to individually stabilize the dimer-prone or monomer-prone conformations, validated in-solution, and

206 dition, the HSA-induced perturbations of the monomer/protofibrils pseudo-equilibrium extend to the C-

207 Such engineered monomers provide a new avenue to probe and manipulate TG

208 the conserved C-terminal tail of the second monomer provides residues essential for catalysis.

209 One monomer provides the SAM-binding site, whereas the conse

210 For example, few single-crystal organic monomers react under topochemical control to produce sin

211 imer are compared to two different ZnTPP-PDI monomer reference systems designed to probe electron tra

212 Incorporation of this unit as a monomer, results with the first class of stimuli-respons

213 studies and crystallography, the engineered monomer retained the same overall structure of native TG

214 boronate ester-linked systems and with broad monomer scope.

215 mechanisms in a one-pot setup and switch the monomer selectivity via an external stimulus provides an

216 al model for the TatA oligomer in which TatA monomers self-assemble using electrostatic 'charge zippe

217 lymers with precisely defined molar mass and monomer sequence (primary structure) have many potential

218 where a high level of molecular precision or monomer sequence control confers potential for molecular

219 fferent end group functionalities as well as monomer sequence distribution (MSD), gradient separation

220 is little understanding of how to translate monomer sequence to physical material properties.

221 anced functions.Nature can precisely control monomer sequences in biopolymers, but this is somewhat p

222 Nature precisely manipulates primary monomer sequences in biopolymers.

223 Furthermore, a perfluorinated photocurable monomer serves as a transparent shell phase with remote

224 lev measures density, and certain classes of monomers show a large change in density when monomers co

225 viral encoded K(+) channel proteins, with a monomer size of only 82 amino acids, resemble the pore m

226 nt appears to enhance both polarization (via monomer solubilization in surfactant micelles) and adher

227 e entire ectodomain of mouse P-selectin as a monomer (sP-selectin) or as a disulfide-linked dimer fus

228 HmAb 5J7 binds to a complex, 3-monomer spanning quaternary epitope in the DENV3 envelop

229 e G-quartet stacks dissociate laterally into monomer stacks without significantly changing the longit

230 rfering with beta2m amyloid formation at the monomer stage, we found that doxycycline and rifamycin S

231 isphenol A glycidyl methacrylate, which is a monomer standard in dental materials, do not support ste

232 ng on the availability of information on the monomer structure, oligomeric state and locations of unr

233 -terminal hexapeptide binding on the Abeta42 monomer structure, which might help in explaining their

234 % (14/17) of the antigen targets using bound monomer structures in docking, 35% (6/17) when using unb

235 tructure database or by ab initio docking of monomer structures resolved by experiment or predicted b

236 With slowly polymerizing monomers (styrene and methyl methacrylate) and initiator

237 ough three disulfide cross-links between the monomer subunits.

238 Using a monomer such as butyl acrylate for the emulsion's oil ph

239 ute by which simple hybrid inorganic-organic monomers, such as compound 1, can spontaneously assemble

240 K28 can cause the release of cytotoxic alpha monomers, suggesting a toxin-intrinsic mechanism of disu

241 nuated by increasing concentrations of actin monomers, suggesting competition between actin and micro

242 Across this interface, one monomer supplied a catalytic arginine to the opposing su

243 n expressed as a soluble protein is mainly a monomer that does not display quaternary epitopes, which

244 we discovered, in grass lignins, a phenolic monomer that falls outside the canonical lignin biosynth

245 main of CrSEPT purified as a nucleotide-free monomer that hydrolyzes GTP and readily binds its analog

246 , which facilitate interactions with another monomer that undergoes conformational changes stabilizin

247 ion of water-insoluble, low-molecular-weight monomers that show a large change in density upon polyme

248 e separately incorporated into heteroditopic monomers that then generate an ABC sequence-controlled s

249 For each VWF monomer, the ADAMTS13 cleavage site is located deeply bu

250 The first example of a PBD monomer, the natural product anthramycin, was discovered

251 of functional imidazolium-type ionic liquid monomers, the polymer membrane protects the metal agains

252 The development of renewable monomers, the versatile synthetic routes to convert thes

253 ctional group, was synthesized from a gemini monomer through photoreaction in the solid state.

254 ophy of Ppmet6 Thus, association of two PpMS monomers through the interaction of Arg-742 and Asp-113

255 Comparisons of the dynamics of ARL2 monomer to ARL2 in the trimer suggested that its protein

256 condary metabolites by iteratively appending monomers to a growing serial oligomer chain.

257 ism that uses cross-talk between the two NDK monomers to accelerate phosphorylation-related assembly

258 eation, the common evolution from disordered monomers to alpha-helices and then to beta-sheets when t

259 -9 act together to aid aggregation of m4-1BB monomers to efficiently initiate m4-1BB signaling.

260 ological ionic strength proceeds from folded monomers to folded antiparallel dimers, tetramers, and h

261 rature synthesis may allow diverse molecular monomers to form single-crystalline packings of polymers

262 versatile synthetic routes to convert these monomers to polyesters and polycarbonate, and the differ

263 er arms are available to recruit and deliver monomers to the filament tip, suggesting that VASP opera

264 The antibody extensively anchors two monomers together at the base of the trimer, and biochem

265 the protein and potentially to the dimer-to-monomer transition.

266 ins of Hendra virus F protein associate in a monomer-trimer equilibrium (Smith, E.

267 our mechanisms corresponding to monosolvated monomers, trisolvated dimers, octasolvated monomers, and

268 Coacervation of the elastin monomer, tropoelastin, in response to heat and salt is a

269 cross-linker outperformed its corresponding monomer twin, establishment of a phase-transfer protocol

270 dimeric transcriptional repressors with each monomer typically containing both structural and regulat

271 apacity of a DNA probe with two inserted UNA monomers (UNA2), and compared it to the DNA probe with t

272 ts capture the interstrand separation within monomer units during the transition from the oligomer to

273 de-free and GDP-bound states, while it forms monomers upon GTP binding, leading to a monomer-dimer cy

274 sed the potential EA of both a new bisphenol monomer used to synthesize polymeric coatings for metal

275 sphenol bis(t-butyldimethylsilyl) ethers (BB monomers) using [Ph3 P=N-PPh3 ](+) [HF2 ](-) as the cata

276 beta configuration of the lactam ring in the monomer via the stereospecific [2+2] cycloaddition of tr

277 This leads to a model in which Vpu monomers, Vpu homooligomers, and Vpu-target heterooligom

278 A novel phenylpiperazine acrylamide monomer was synthesized and chain extended using atom tr

279 Even under conditions in which the LiHMDS monomer was the dominant observable form, dimer-based me

280 The synthesis of the fluoranthene monomers was carried out using a divergent strategy that

281 only considered divalent ureidopyrimidinone monomers we now present a model-driven engineering appro

282 , and as m4-1BBL can only recruit two m4-1BB monomers, we hypothesize that m4-1BBL and Gal-9 act toge

283 Pre-organized gemini monomers were irradiated with UV light and monitored by

284 yl fluoride and amines/anilines while the BB monomers were obtained from silylation of bisphenols by

285 The AA monomers were prepared via the highly reliable Michael a

286 ons induce conformational transitions of the monomer, which facilitate interactions with another mono

287 by copolymerization of amine functionalized monomer, which is indispensable to the enzyme immobiliza

288 mobilization, with palladium complex bearing monomer, which is mediate the bioelectrocatalytic reacti

289 opolymerization of acrylamide and functional monomers, which are dynamically complexed with the host

290 e reduction of cytosolic NPR1 oligomers into monomers, which enter the nucleus and function as transc

291 easing the concentration of functional apoE4 monomers, which gives rise to its higher lipid binding c

292 re frequently populated within the A2T-bound monomer, while A2V-bound Abeta42 is often enhanced in ov

293 tional entanglements from newly incorporated monomers, whose key features can be recapitulated with m

294 ycol has one Ca(2+) ion resolved within each monomer with a constricted pore; this is likely to corre

295 ed metastable state was an unfolded, compact monomer with little similarity to the native structure.

296 chemically polymerizing a conducting polymer monomer with ssDNA probe sequence pre-attached.

297 tridium perfringens that cleaves sialic acid monomers with an alpha2-3,6,8,9 linkage, which is simila

298 tris(2-aminoethyl amine)), semi-fluorinated monomers with side chains containing between three and 2

299 stable dimers, ClC-4 was mostly observed as monomer, with ClC-3-ClC-4 heterodimers being more stable

300 ture shows that ZIKV-117 Fabs cross-link the monomers within the surface E glycoprotein dimers as wel

301 Dicyclopropyl ketone added rapidly to the monomers (Z)-1&3THF and (E)-1&3THF with a rate ratio of